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  • wheat  (55)
  • gene expression  (54)
  • Springer  (108)
  • American Chemical Society
  • 2005-2009
  • 1990-1994  (108)
  • 1980-1984
  • 1925-1929
  • 1994  (108)
  • 1926
Collection
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  • 2005-2009
  • 1990-1994  (108)
  • 1980-1984
  • 1925-1929
Year
  • 1
    Electronic Resource
    Electronic Resource
    DNA in wheat seeds from European archaeological sites (1994)
    Springer
    Cellular and molecular life sciences 50 (1994), S. 571-575 
    Details
    ISSN: 1420-9071
    Keywords: Ancient DNA ; archaeobotany ; carbonized grain ; DNA sequences ; glutenin alleles ; seed proteins ; Triticum ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We have used hybridization analysis to detect ancient DNA in wheat seeds collected from three archaeological sites in Europe and the Middle East. One of these samples, carbonizedT. spelta dated to the first millennium BC, has yielded PCR products after amplification with primers directed at the leader regions of the HMW (high molecular weight) glutenin alleles. Sequences obtained from these products suggest that the DNA present in the Danebury seeds is chemically damaged, as expected for ancient DNA, and also indicate that it should be possible to study the genetic variability of archaeological wheat by ancient DNA analysis. Finally, we describe a PCR-based system that enables tetraploid and hexaploid wheats to be distinguished.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01921727
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  • 2
    Electronic Resource
    Electronic Resource
    Effect of radical scavengers on TNFα-mediated activation of the uPA in cultured cells (1994)
    Springer
    Cellular and molecular life sciences 50 (1994), S. 958-962 
    Details
    ISSN: 1420-9071
    Keywords: Plasminogen activator ; active oxygen ; gene expression ; radical scavengers ; endothelial cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Active oxygen, produced by cultured cells following stimulation with various growth factors, seems to be involved in signal transduction leading to cellular responses such as gene expression and growth modulation. In the present study, the intracellular oxidation state was measured in immortalized human endothelial cells (ECV304) after treatment with tumor necrosis factor (TNF)α, using a fluorescent dye and a laser-scanning confocal microscope. The intracellular oxidation state was increased 60 min after the addition of TNFα, and this increase was abolished by a radical scavenger, N-acetylcysteine (NAC), which is also a precursor of glutathione, and by pyrrolidine dithiocarbamate (PDTC). TNFα increased the steady state level of urokinase-type plasminogen activator (uPA), and NAC inhibited this increase at a dose that also inhibited the increase in the intracellular oxidation state. PDTC, on the other hand, did not affect the induction of the uPA gene by TNFα. These results suggest that intracellular glutathione level rather than the oxidation state is necessary for the induction of the uPA gene by TNFα.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01923487
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  • 3
    Electronic Resource
    Electronic Resource
    Assessing risk associated with N fertilizer recommendations in the absence of soil tests (1994)
    Springer
    Nutrient cycling in agroecosystems 40 (1994), S. 175-183 
    Details
    ISSN: 1573-0867
    Keywords: Nitrogen response ; on-farm research ; risk ; probability ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract In many developing countries, fertilizer recommendations must be made in the absence of plant and soil analyses. When the region is variable in terms of soils, weather, and magnitude of response to fertilizer, a recommendation is likely to involve a high degree of risk for the farmer. Quantification of such risk is key to developing appropriate recommendations for the farmer. However, most methodologies generally used in analyzing fertilizer trials do not allow adequate quantification, especially as a continuous function, of the risk associated with a given recommendation. Three years of on-farm trials conducted in the High Valley of Mexico were used to evaluate different methodologies for generating N fertilization recommendations and their associated risk for wheat (Triticum aestivum) production in the absence of soil tests. When the traditional approach, using average yield responses or separate trial results, was used, an economic optimum was identified, but it was not possible to quantify the associated risk. In contrast, however, by using a combination of response surface methodology and simple probability analysis, the risk associated with any given recommendation was developed, even under the highly variable conditions of the study zone. The approach uses a treatment difference matrix (developed using average yield differences between a treatment and the zero N (0N) check) and its associated standard deviation over locations. From the matrix, an equation (being a function of N rate and relative grain:N price ratios) was developed that shows the probability of outperforming the 0N check for the economic optimum rate.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00750463
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  • 4
    Electronic Resource
    Electronic Resource
    Effect of soil pH on the requirement for water-soluble phosphorus in triple superphosphate fertilizers (1994)
    Springer
    Nutrient cycling in agroecosystems 40 (1994), S. 207-214 
    Details
    ISSN: 1573-0867
    Keywords: available P ; citrate insoluble P ; phosphorus sources ; triple superphosphate ; Triticum aestivum ; water soluble P ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A greenhouse study was conducted to determine if soil pH affects the requirement for water-soluble P and the tolerance of water-insoluble impurities in TSP fertilizers. Two commercial TSP fertilizers were selected to represent a range in phosphate rock sources and impurities. Phosphate fertilizer impurities were isolated as the water-washed fraction by washing whole fertilizers with deionized water. TSP fertilizers with various quantities of water-soluble P (1.2 to 99% water-soluble P) were simulated by mixing the water-washed fertilizer fractions or dicalcium phosphate (DCP) with reagent-grade monocalcium phosphate (MCP). The fertilizers were applied to supply 40 mg AOAC available P kg−1 to a Mountview silt loam (fine-silty, siliceous, thermic Typic Paleudults). Wheat (Triticum aestivum (L.)) was harvested at 49 and 84 days after planting. Soil pH values at the final forage harvest were 5.4±0.16 and 6.4±0.15. At a soil pH of 5.4, the TSP fertilizers required only 37% water-soluble P to reach maximum yields while at pH 6.4 the fertilizers required 63% water-soluble P. Results of this study show that higher levels of water -insoluble P can be tolerated in TSP fertilizers when applied to acid soils. Phosphorus uptake was not affected by soil pH, but for the mixtures containing the fertilizer residues the source having the lowest level of Fe and Al had a higher relative agronomic effectiveness.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00750467
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  • 5
    Electronic Resource
    Electronic Resource
    Wheat growth from phosphorus fertilizers as affected by time and method of application in soil with an acidic subsurface layer (1994)
    Springer
    Nutrient cycling in agroecosystems 39 (1994), S. 77-82 
    Details
    ISSN: 1573-0867
    Keywords: Acidic subsurface layer ; application rate ; North Carolina phosphate rock ; placement method ; time of application ; triple superphosphate ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Using soils with an acidic subsurface layer, three glasshouse experiments were carried out to evaluate the effect of placement method and application rate of triple superphosphate (TSP) and North Carolina phosphate rock (NCPR) on dry matter (DM) yields. Time of application of NCPR on DM yield response of wheat was also studied. For Experiment 1, soil was collected in depth intervals of 0–2; 4–6; 6–8; and 8–10 cm from a red earth (chromic luvisol). The treatments included two P sources (TSP and NCPR), three placement methods (broadcast, banded or mixed into the subsurface layer, 6–8 cm), and six application rates. In this P deficient soil with an acidic subsurface layer, there was relatively little effect of application method of TSP on wheat yield responses. The maximum dry matter yield responses for broadcast, band and mix application methods was 30, 42 and 50 %, respectively. Responses to NCPR broadcast, band and mix methods were 20, 9 and 44 %, respectively. Mixing NCPR into to acidic subsurface layer produced yields similar to those from TSP although a higher application rate of P as NCPR was needed to achieve this outcome. Treatments for Experiments 2 and 3 were time of application of NCPR (0 and 30 days before sowing) and rate of application of NCPR (0 and 40 mg P/pot). In Experiment 2 (same soil as Experiment 1) application of NCPR prior to sowing, resulted in higher Colwell P concentration than when applied at sowing, but time of application had no effect on final DM yields. Experiment 3 used a red podzolic (chromic luvisol) soil which had a lower P-status, was more acid and had a lower exchangeable Ca2+ concentration than the red earth. Application of NCPR prior to sowing resulted in lower DM yield than when it was applied prior to sowing.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00750159
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  • 6
    Electronic Resource
    Electronic Resource
    The residual effectiveness of previously applied copper fertiliser for grain yield of wheat grown on soils of south-west Australia (1994)
    Springer
    Nutrient cycling in agroecosystems 39 (1994), S. 11-18 
    Details
    ISSN: 1573-0867
    Keywords: Copper fertiliser ; nitrogen fertiliser ; residual effectiveness ; Triticum aestivum L. ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The residual effectiveness of copper (Cu) applied 18 to 21 years previously was estimated for grain yield of wheat. In one field experiment, current levels of Cu fertiliser were applied and its effectiveness was compared to that of the same level of Cu applied previously. The effects of nitrogen (N) fertiliser on the Cu concentration in the youngest emerged blade and in the grain, as well as the effects of N levels on the grain yield of wheat, were also studied. Where the recommended level of Cu fertiliser had been applied previously, its residual effectiveness depended on the soil type. On the grey sands over clay and gravelly sands over clay, the residual Cu would last approximately 20 years where wheat is grown in rotation with a legume crop (Lupinus augustifolius L.) and where N fertiliser is applied at high levels (92 kg N ha−1). On the yellow brown sandy earths of the Newdegate district, the residual value was in excess of 30 years. When Cu levels in the soil are marginal, high levels of N applied to wheat crops grown on stubbles of legume crops (high soil N) could suffer from induce Cu deficiency which could reduce grain production. Critical concentrations of Cu in the youngest emerged blade of less than 1.2 mg Cu kg−1 at Gs50–59 would indicate Cu deficiency. Cu concentrations of less than 1.1–1.2 mg Cu kg−1 in the grain suggest that the wheat crop is marginally supplied with Cu. In both situations, Cu fertiliser needs to be applied before the next crop.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00750152
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  • 7
    Electronic Resource
    Electronic Resource
    Penicillium bilaji and phosphorus fertilization effects on the growth, development, yield and common root rot severity of spring wheat (1994)
    Springer
    Nutrient cycling in agroecosystems 39 (1994), S. 97-103 
    Details
    ISSN: 1573-0867
    Keywords: Cochliobolus sativus ; common root rot ; Penicillium bilaji ; phosphorus fertilization ; tillering ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A strain ofPenicillium bilaji Chalabuda (PB) has recently been commercially released as a seed inoculant to increase phosphorus (P) uptake by wheat (Triticum aestivum L.). The purpose of this study was to compare the effects of drill applied P (15 kg P ha−1) with PB seed inoculation on early growth, development, P uptake, and grain yield of ‘Stoa’ spring wheat at four sites in North Dakota. Fertilization with P consistently enhanced early season growth, main stem development, tillering and P uptake. Seed inoculation with PB had little or no effect on these traits. Phosphorus fertilization tended to increase common root rot severity (CRR, incited byCochliobolus sativus (Ito & Kurib) Drechs.), while PB inoculation had no effect. Grain yields were significantly increased by P fertilization at one location. Inoculation with PB also increased grain yield at this location. The reason why PB inoculation increased yield at this location is not evident, as plant growth and P uptake were not enhanced earlier in the season. Averaged across all four sites, PB inoculation increased wheat yields 66 kg ha−1, which is similar to averaged yield responses reported from the Prairie Provinces of Canada.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00750908
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  • 8
    Electronic Resource
    Electronic Resource
    Expression of calcium-binding protein regucalcin mRNA in rat liver is stimulated by calcitonin: The hormonal effect is mediated through calcium (1994)
    Springer
    Molecular and cellular biochemistry 136 (1994), S. 43-48 
    Details
    ISSN: 1573-4919
    Keywords: regucalcin ; calcium-binding protein ; gene expression ; rat liver
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The involvement of a hypocalcemic hormone calcitonin (CT) in the expression of hepatic Ca2+-binding protein regucalcin mRNA was investigated. The change of regucalcin mRNA levels was analyzed by Northern blotting using liver regucalcin complementary DNA (0.9 kb). A single oral administration of calcium chloride (100 mg Ca/100 g body weight) to rats induced a remarkable increase in the serum calcium concentration and a corresponding elevation of the liver calcium content during 120 min after the administration. Thyroparathyroidectomy (TPTX) did not cause a significant increase in the liver calcium content after calcium administration. Hepatic regucalcin mRNA level was markedly elevated by calcium administration; the level was about 180% of controls at 60 min after the administration. This increase was completely abolished by TPTX. A single subcutaneous administration of CT (synthetic eel CT; 25–100 MRC mU/100 g) to TPTX rats received oral administration of calcium (100 mg/100 g) produced a remarkable increase in hepatic regucalcin mRNA levels; the level was about 280% of controls with the dose of 25 MRC mU CT/100 g. The present finding suggests that the expression of hepatic mRNA is stimulated by CT, and that the hormonal effect is mediated through Ca2+ in rat liver.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00931603
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  • 9
    Electronic Resource
    Electronic Resource
    Expression of hepatic calcium-binding protein regucalcin mRNA is decreased by phenobarbital administration in rats (1994)
    Springer
    Molecular and cellular biochemistry 141 (1994), S. 15-19 
    Details
    ISSN: 1573-4919
    Keywords: regucalcin ; calcium-binding protein ; gene expression ; phenobarbital ; rat liver
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The effect of phenobarbital on the expression of calcium-binding protein regucalcin mRNA in rat liver was investigated. The change of regucalcin mRNA levels was analyzed by Northern blotting using liver regucalcin cDNA (0.9 kb of open reading frame). Phenobarbital (4, 8 and 12 mg/ 100 g body weight) was intraperitoneally administered to rats 3 times with 24 h intervals, and the animals were sacrificed by bleeding at 24 h after the last administration. The hepatic regucalcin mRNA levels were markedly reduced by phenobarbital administration. This decrease was about 50% of control level with the 12 mg/100 g dose. Moreover, the hepatic regucalcin concentration was significantly decreased by the administration of phenobarbital (12 mg/100 g), although the serum regucalcin concentration was not altered appreciably. Meanwhile, serum transaminases (GOT and GPT) activities were not increased by the administration of phenobarbital (4 and 12 mg/100 g). The present study demonstrates that the expression of hepatic regucalcin mRNA is decreased by phenobarbital administration in rats, suggesting that regucalcin does not have a role in drug metabolism related to phenobarbital.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00935586
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  • 10
    Electronic Resource
    Electronic Resource
    Regulation of mRNA transcripts and DNA synthesis in the rat heart following intravenous injection of transforming growth factor beta1 (1994)
    Springer
    Molecular and cellular biochemistry 141 (1994), S. 145-151 
    Details
    ISSN: 1573-4919
    Keywords: pressure overload ; myocardium ; gene expression ; fibroblast ; extracellular matrix ; ventricular hypertrophy ; growth factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Transforming Growth Factor-beta1 (TGF-β1) is expressed in the heart by muscle and non-muscle cardiac cells.In vitro, cardiac myocytes and non-muscle cells including cardiac fibroblasts and endothelial cells respond to regulatory effects of TGF-β1. Expression of TGF-β1 in the heart is subject to regulation by hemodynamic stimuli. Increased expression of mRNA transcripts for TGF-β1 has been reported in several models of cardiac hypertrophy. The objective of this study was to determine the effect of TGF-β1 in the myocardium. TGF-β1 was injected intravenously. Expression of mRNA transcripts for functional and structural proteins was determined by Northern hybridization analysis. DNA synthesis was determined by measurement of3H-thymidine incorporation into ventricular DNA. The results showed differential regulation of mRNAs for myocyte- and non-myocyte-specific proteins in the heart of TGF-β1 treated rats. Moderate but statistically significant decrease in DNA synthesis was observed in the heart of TGF-β1 treated rats (37.5%, P〈0.025). Together, these data point to a physiological role for TGF-β1 in the heart. They further suggest that similar to its diversein vitro cell-specific regulatory effects, TGF-β1 may have multicellular targets in the heart. Effect of TGF-β1 alone or combined with those of other cytokines/hormones that come into play, as the result of its administration, may be responsible for altered gene expression and DNA synthesis in the myocardium. We propose that in experimental models of myocardial hypertrophy which are associated with increased expression of TGF-β1 in the heart, the contribution of regulatory effects of this growth factor to the manifestations of ventricular hypertrophy could be significant.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00926178
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  • 11
    Electronic Resource
    Electronic Resource
    Calcium and calcium-binding proteins in the nucleus (1994)
    Springer
    Molecular and cellular biochemistry 135 (1994), S. 79-88 
    Details
    ISSN: 1573-4919
    Keywords: calcium ; nucleus ; calpain ; calmodulin ; cell division ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Calcium has long been known to play a role as a key cytoplasmic second messenger, but until relatively recently its possible involvement in nuclear signal transduction and the regulation of nuclear events has not been extensively studied. Evidence revealing the presence of transmembrane nuclear Ca2+ gradients and a variety of intranuclear Ca2+ binding proteins has fueled renewed interest in this key ion and its involvement in cell-cycle timing and division, gene expression, and protein activation. This review will offer an overview of the current state of knowledge and theory regarding calcium orchestration of nuclear functions and events and discuss possible future directions in this field of study.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00925963
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  • 12
    Electronic Resource
    Electronic Resource
    Transcriptional regulation and autoregulation of the human gene for ADP-ribosyltransferase (1994)
    Springer
    Molecular and cellular biochemistry 138 (1994), S. 99-104 
    Details
    ISSN: 1573-4919
    Keywords: poly(ADP-ribosyl) transferase (human) ; autoregulation ; gene expression ; promoter structure ; cruciform structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Human nuclear poly(ADP-ribosyl)transferase (ADPRT) modifies proteins with branched ADP-ribose-polymers. Various proteins, including ADPRT itself, serve as acceptors for polyADP-ribose. Target proteins include those controlling basic cellular processes such as DNA repair, differentiation and proliferation. Because of the outstanding features of this enzyme: automodification, several functional domains and central role in physiology of the cell, the molecular biology of ADPRT gained wide interest. The promoter structure contains several CCAAT/TATA boxes and SP1 sites. However, there is no CCAAT/TATA box in the neighbourhood of an SP1 site and, thus no obvious site for initiation of transcription. Within this region there are several noteworthy inverted repeats, which by internal basepairing could form two types of cruciform structures. Deletion analysis revealed that these cruciform structures have functional significance. Removal of one type increases the promoter activity, whereas removal of the other diminishes the promoter function. Overexpression of ADPRT from heterologous promoters (MMTV, SV40) leads to repression of the activity of the ADPRT promoter. Indeed, ADPRT was shown to bind specifically to one type of cruciform structure. This specific interaction indicates autorepression of the ADPRT gene: the enzyme ADPRT acts directly as a negative modulator of the activity of its own promoter.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00928449
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  • 13
    Electronic Resource
    Electronic Resource
    Expression of the mitochondrial creatine kinase genes (1994)
    Springer
    Molecular and cellular biochemistry 133-134 (1994), S. 235-243 
    Details
    ISSN: 1573-4919
    Keywords: creatine kinase ; mitochondria ; metabolism ; creatine phosphate shuttle ; gene expression ; muscle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Mitochondrial Creatine Kinase (MtCK) is responsible for the transfer of high energy phosphate from mitochondria to the cytosolic carrier, creatine, and exists in mammals as two isoenzymes encoded by separate genes. In rats and humans, sarcomere-specific MtCK (sMtCK) is expressed only in skeletal and heart muscle, and has 87% nucleotide identity across the 1257 bp coding region. The ubiquitous isoenzyme of MtCK (uMtCK) is expressed in many tissues with highest levels in brain, gut, and kidney, and has 92% nucleotide identity between the 1254 bp coding regions of rat and human. Both genes are highly regulated developmentally in a tissue-specific manner. There is virtually no expression of sMtCK mRNA prior to birth. Unlike cytosolic muscle CK (MCK) and brain CK (BCK), there is no developmental isoenzyme switch between the MtCKs. Cell culture models representing the tissue-specific expression of either sMtCK or uMtCK are available, but there are no adequate developmental models to examine their regulation. Several animal models are available to examine the coordinate regulation of the CK gene family and include 1) Cardiac Stress by coarctation (sMtCK, BCK, and MCK), 2) Uterus and placenta during pregnancy (uMtCK and BCK), and 3) Diabetes and mitochondrial myopathy (sMtCK, BCK, and MCK). We report the details of these findings, and discuss the coordinate regulation of the genes necessary for high-energy transduction.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01267957
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  • 14
    Electronic Resource
    Electronic Resource
    Nuclear Ca2+: physiological regulation and role in apoptosis (1994)
    Springer
    Molecular and cellular biochemistry 135 (1994), S. 89-98 
    Details
    ISSN: 1573-4919
    Keywords: calcium ; cell death ; nuclei ; apoptosis ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The last decade has seen the rapid development of research investigating the molecular mechanisms whereby hormones, peptide growth factors and cytokines regulate cell metabolism, differentiation and proliferation. One general signalling mechanism used to transfer the information delivered by agonists into appropriate intracellular compartments involves the rapid Ca2+ redistribution throughout the cell, which results in transient elevations of the cytosolic free Ca2+ concentration. Ca2+ signals are required for a number of cellular processes including the activation of nuclear processes such as gene transcription and cell cycle events. The latter require that appropriate Ca2+ signals elicited in response to agonists be transduced across the nuclear envelope. It has generally been assumed that small molecules, metabolites and ions could freely diffuse across the nuclear envelope. Nevertheless several findings during the past few years have suggested that nuclear pore permeability can be regulated and that ion transport systems and ion-selective channels may exist on the nuclear membranes and regulate intranuclear processes. Intranuclear Ca2+ fluctuations can affect chromatin organization, induce gene expression and also activate cleavage of nuclear DNA by nucleases during programmed cell death or apoptosis. The possible mechanisms involved in nuclear Ca2+ transport and the control of nuclear Ca2+-dependent enzymes in apoptosis is discussed below.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00925964
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  • 15
    Electronic Resource
    Electronic Resource
    A retinoic acid-inducible skin-specific gene (RIS-1/psoriasin): molecular cloning and analysis of gene expression in human skinin vivo and cultured skin cellsin vitro (1994)
    Springer
    Molecular biology reports 20 (1994), S. 75-83 
    Details
    ISSN: 1573-4978
    Keywords: retinoic acid ; skin ; differential hybridization ; cloning ; keratinocytes ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A retinoic acid (RA) inducible skin-specific gene transcript (RIS-1) was isolated by differential hybridization screening of a RA-treated human skin cDNA library. The library was constructed from pooled RNA derived from normal adult human skin treated with alltrans-RA for 4 h (n=6) and 12 h (n=6)in vivo. RIS-1 cDNA corresponded to a 0.6 kb transcript that was barely detectable in normal adult human skin but was significantly induced by 8 h in RA-treated compared to vehicle-treated skin (range 1.1–3.6 fold). Prolonged RA treatment for up to 24 h further increased relative RIS-1 mRNA levels by 1.3–5.5 fold. HPLC analysis of the RA content of 0.1% RA-treated skinin vivo revealed significant levels at 6 h (18.8–120.6 ng RA/g wet weight tissue; approximately 240 nM), immediately preceding the time point at which the increased RIS-1 mRNA level was first seen. This concentration of RA also induced the mRNA levels for cellular RA binding protein II (1.6–19 fold), a marker of RA activity in human skin. RIS-1 mRNA was detected by Northern and dot blotting only in normal skin but not in any other normal human tissues examined, indicating a tissue-specific pattern of gene expression. RIS-1 transcripts were detected at very low levels in untreated cultured human epidermal keratinocytes, while no expression was seen in dermal fibroblasts and melanocytes, the other major cell types in skin. Southern analysis of human and mouse DNA indicated the existence of evolutionarily conserved sequences for RIS-1 between these two species. The polypeptide sequence derived from the partial RIS-1 cDNA was found to be identical to the calcium binding domain found in ‘psoriasin’, a gene whose expression appears to be increased in the skin of psoriasis patients.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00996356
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  • 16
    Electronic Resource
    Electronic Resource
    Expression of nitrate assimilation related genes in Chlamydomonas reinhardtii (1994)
    Springer
    Plant molecular biology 24 (1994), S. 185-194 
    Details
    ISSN: 1573-5028
    Keywords: gene expression ; light/nitrate regulation ; nitrate reductase ; nitrate transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The mRNA accumulation pattern of the Chlamydomonas reinhardtii nitrate assimilation-related gene cluster has been elucidated. In ammonium-grown wild-type cells, nit-1 (nitrate reductase, NR), nar-1, nar-2 and nar-3 (nitrate transporter) genes showed very similar kinetics of expression when transferred to nitrate medium. Transcripts of all these genes accumulated transiently in ammonium-grown wild-type cells after a one-hour incubation in nitrogen-free medium, and practically disappeared at about 2 hours. Mutant strains lacking functional nitrate reductase showed similar accumulation kinetics of these transcripts during both nitrate induction and derepression in nitrogen-free media. In contrast to the other nar transcripts, that nar-4, a gene sharing similar sequences with nar-3, accumulated in small amounts in wild-type cells, and only increased after a long nitrate induction period. Nitrate and light showed a strong positive effect on the accumulation of nit-1 gene transcripts. Acetate as a carbon source allowed accumulation of nit-1 mRNA in the dark, indicating the existence of interactions between light and carbon metabolism in nit-1 gene expression. Our data strongly suggest that NR negatively autoregulates its own expression and that of nar genes.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00040584
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  • 17
    Electronic Resource
    Electronic Resource
    Expression of one of the members of the Arabidopsis chaperonin 60β gene family is developmentally regulated and wound-repressible (1994)
    Springer
    Plant molecular biology 24 (1994), S. 195-202 
    Details
    ISSN: 1573-5028
    Keywords: plant transformation ; chaperonin 60β ; β-glucuronidase ; wound repression ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract To study the pattern of gene regulation of the plastid chaperonin 60β gene family a chimaeric gene was constructed fusing the 5′-flanking region of the chaperonin 60β B3 gene to the β-glucuronidase reporter gene. Histochemical and fluorometric analysis of the GUS activity present in transgenic plants harbouring this gene construct showed that the B3 promoter is expressed in leaves, stem, petioles and several flower tissues. The pattern of cell type-specific expression in stems and flowers was found to be developmentally regulated. Expression of the B3 promoter was found not to be heat-inducible, but highly repressed by wounding. The rapid decay in GUS activity upon wounding indicates that, at least under some physiological conditions, the gene product of this reporter gene is not as stable as has been previously thought.
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    URL: http://dx.doi.org/10.1007/BF00040585
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    Homologues of wheat ubiquitin-conjugating enzymes - TaUBC1 and TaUBC4 are encoded by small multigene families in Arabidopsis thaliana (1994)
    Springer
    Plant molecular biology 24 (1994), S. 651-661 
    Details
    ISSN: 1573-5028
    Keywords: protein degradation ; ubiquitin conjugating enzymes ; DNA repair ; N-end recognition ; wheat ; Arabidopsis thaliana
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Covalent attachment of ubiquitin to other cellular proteins has been implicated in a multitude of diverse physiological processes in eukaryotes including selective protein degradation. This attachment is carried out by a multi-enzyme pathway consisting of three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-conjugating enzymes (E2s), and ubiquitin-protein ligases (E3s). E2s accept activated ubiquitin from E1 and conjugate it to target proteins with or without the participation of specific E3s. Previously, we have isolated wheat cDNAs encoding 16 and 23 kDa E2s, TaUBC1 and TaUBC4, respectively. TaUBC1 shows structural homology to the yeast RAD6 E2 that is essential for DNA repair whereas TaUBC4 is related to the yeast ScUBC8 E2, both of which effectively conjugate ubiquitin to histones in vitro but as yet are without a known in vivo function. Here, we report the isolation of genomic and cDNA homologues of these genes from Arabidopsis thaliana. In Arabidopsis, both of these E2s are encoded by three member gene families. Members of the AtUBC1 gene family, comprising AtUBC1, 2 and 3, encode 150–152 amino acid proteins that are 83–99% identical to each other and TaUBC1 and contain four introns that are conserved with respect to position. Members of the AtUBC4 gene family, comprising AtUBC4, 5 and 6, encode 187–191 amino acid proteins that are 73–88% identical to each other and TaUBC4 and contain five introns that are conserved with respect to position. In contrast, AtUBC1-3 gene products are only 31–36% identical to those derived from AtUBC4-6. mRNA for each family was detected in Arabidopsis roots, leaves, stems, and flowers indicating that members of each family are expressed in most if not all tissues.
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    URL: http://dx.doi.org/10.1007/BF00023561
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  • 19
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    Low-temperature-responsive barley genes have different control mechanisms (1994)
    Springer
    Plant molecular biology 24 (1994), S. 879-888 
    Details
    ISSN: 1573-5028
    Keywords: barley ; cold acclimation ; gene expression ; low temperature genes ; nuclear run-on transcription
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Several low-temperature-responsive (LTR) genes from barley have been shown to have high steady-state transcript levels. Run-on transcription was used to determine the control of expression of these LTR genes. Six of these are shown to be transcriptionally regulated (blt 4/9, blt 101, blt 1015, blt 63, blt 49, blt 410) whilst three are post-transcriptionally regulated (blt 14, blt 411, blt 801). Two transcriptionally regulated genes (blt 4/9 and blt 101) and one post-transcriptionally regulated gene (blt 14) have been used in expression studies. The time course for the appearance and decay of these transcripts is given. Initial appearance and steady-state levels of individual transcripts have different temperature characteristics but no single gene correlates with the cold acclimation response. We suggest that these different response profiles may represent a means of fine-tuning the low-temperature response. One gene, blt 4/9, also accumulated high steady-state levels of transcript in response to drought and a nutrient stress. However, only drought has an acclimating effect on barley plants.
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    URL: http://dx.doi.org/10.1007/BF00014442
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  • 20
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    The 24kDa outer envelope membrane protein from spinach chloroplasts: molecular cloning, in vivo expression and import pathway of a protein with unusual properties (1994)
    Springer
    Plant molecular biology 25 (1994), S. 167-177 
    Details
    ISSN: 1573-5028
    Keywords: Spinacia oleracea ; chemical cleavage ; gene expression ; polymerase chain reaction ; protein transport ; SDS-PAGE
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The 24 kDa outer envelope membrane protein of spinach chloroplasts (omp24) represents a major constituent of this membrane. Sequences of tryptic and endoprotease Glu-C peptides derived from omp24 allowed the design of oligonucleotides which were used to generate a DNA fragment by polymerase chain reaction using spinach cDNA as template. This fragment served as a probe to screen a cDNA library for a full-length clone of the omp24 coding sequence. The protein predicted from the complete sequence only has 148 amino acids and a molecular mass of 16294 Da. It is an acidic protein (calculated isoelectric point 4.8) with a high content of proline residues. Expression of the coding sequence in Escherichia coli and characterization of the purified recombinant protein produced revealed that the overestimation of its molecular mass by SDS-PAGE (ca. 25 kDa) is due to its abnormal amino acid composition. Despite its rather low hydrophobicity (polarity index 49%), omp24 appears to be deeply embedded in the outer membrane. Insertion of omp24 into the membrane proceeds almost independently of surface receptors or targeting sequence but, in contrast to other known outer envelope membrane proteins, is stimulated by ATP.
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    URL: http://dx.doi.org/10.1007/BF00023235
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  • 21
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    Gene expression of nitrite reductase in Scots pine (Pinus sylvestris L.) as affected by light and nitrate (1994)
    Springer
    Plant molecular biology 25 (1994), S. 449-457 
    Details
    ISSN: 1573-5028
    Keywords: gene expression ; light ; nitrate ; nitrite reductase ; Pimus sylvestris L.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A partial cDNA clone (PSnir) encoding the C-terminal region of nitrite reductase was isolated from a λgt 11 library of the gymnospermPimus sylvestris (L.). Nucleotide sequence analysis showed that PSnir contains a reading frame encoding 105 amino acid residues. The amino acid sequence revealed a homology to NiR of 63–68% to dicotyledoneous and of 57–59% to monocotyledoneous species. The protein region implicated to be involved in binding of the prosthetic group is highly conserved between the NiR of the gymnosperm and of angiosperms. In all organs (cotyledonary whorls, hypocotyls, roots) the pattern of NiR gene expression in response to nitrate and light is the same at the level of transcript accumulation and at the enzyme level. This suggests that regulation of NiR gene expression in the Scots pine seedling is predominantly at the level of transcript accumulation. The highest NiR appearance was observed in roots and hypocotyls. In the cotyledonary whorls only small amounts of NiR were found. In roots and hypocotyls the accumulation of NiR mRNA and the appearance of NiR protein is mainly controlled by nitrate, whereas the regulation of NiR gene expression in the whorls is strongly affected by light and the inducive effect of nitrate is only weak.
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    URL: http://dx.doi.org/10.1007/BF00043873
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    Isolation and characterization of two tightly linked catalase genes from castor bean that are differentially regulated (1994)
    Springer
    Plant molecular biology 25 (1994), S. 507-516 
    Details
    ISSN: 1573-5028
    Keywords: castor bean (Ricinus communis) ; catalase gene ; gene expression ; germination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two catalase genes,cat1 andcat2, have been isolated from the castor bean genome. They were located in the same direction on a chromosome at a distance of 2.4 kb,cat1 being on the downstream side ofcat2. The two genes contained introns at the same positions except that one of the 7 introns incat1 is missing incat2 and the corresponding introns differed in size and sequence between the two genes. The translated regions of the two genes had the same number of nucleotides and exhibited 81.3% nucleotide sequence identity. In addition to introns, the nucleotide sequences of the 5′-and 3′-flanking regions are highly divergent between the two genes. In etiolated seedlings,cat1 mRNA was present abundantly in endosperms and cotyledons and only in a small amount in roots. Thecat1 mRNA could not be detected in hypocotyls. By contrast,cat2 mRNA is most abundant in hypocotyls and roots, while endosperms and cotyledons contained only low levels ofcat2 mRNA. Although neithercat1 norcat2 mRNA could be detected in dry seeds, both mRNAs showed temporal accumulation in the endosperm in response to germination. These results suggest that expression of two tightly linked catalase genes of castor bean,cat1 andcat2, are differentially regulated during development.
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    URL: http://dx.doi.org/10.1007/BF00043878
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    Characterization of four new β-tubulin genes and their expression during male flower development in maize (Zea mays L.) (1994)
    Springer
    Plant molecular biology 24 (1994), S. 295-315 
    Details
    ISSN: 1573-5028
    Keywords: β-tubulin ; microtubules ; maize ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Four different β-tubulin coding sequences were isolated from a cDNA library prepared from RNA from maize seedling shoots. The four genes (designated tub4, tub6, tub7 and tub8) represented by these cDNA clones together with the tub1 and tub2 genes reported previously encode six β-tubulin isotypes with 90–97.5% amino acid sequence identity. Results from phylogenetic analysis of 17 β-tubulin genes from monocot and dicot plant species indicated that multiple extant lines of β-tubulin genes diverged from a single precursor after the appearance of the two major subfamilies of α-tubulin genes described previously. Hybridization probes from the 3′ non-coding regions of six β-tubulin clones were used to quantify the levels of corresponding tubulin transcripts in different maize tissues including developing anthers and pollen. The results from these dot blot hybridization experiments showed that all of the β-tubulin genes were expressed in most tissues examined, although each gene showed a unique pattern of differential transcript accumulation. The tub1 gene showed a high level of transcript accumulation in meristematic tissues and almost no accumulation in the late stages of anther development and in pollen. In contrast, the level of tub4 transcripts was very low during early stages of male flower development but increased markedly (more than 100 times) during the development of anthers and in pollen. Results from RNAse protection assays showed that this increased hybridization signal resulted from expression of transcripts from one or two genes closely related to tub4. The tub4-related transcripts were not present in shoot tissue. Transcripts from the tub2 gene accumulated to very low levels in all tissues examined, but reached the highest levels in young anthers containing microspore mother cells. RNAse protection assays were used to measure the absolute levels of α- and β-tubulin transcripts in seedling shoot and in pollen. The α-tubulin gene subfamily I genes (tua1, tua2, tua4) contributed the great majority of α-tubulin transcripts in both shoot and pollen. Transcripts from the β-tubulin genes tub4, tub6, tub7, and tub8 were predominant in shoot, but were much less significant than the tub4-related transcripts in pollen.
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    URL: http://dx.doi.org/10.1007/BF00020169
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    Structural and functional analysis of an Opaque-2-related gene from sorghum (1994)
    Springer
    Plant molecular biology 24 (1994), S. 515-523 
    Details
    ISSN: 1573-5028
    Keywords: gene expression ; b-ZIP motif ; seed storage proteins ; trans-acting factors ; transcription factors ; transcriptional regulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The Opaque-2 (O2) gene from maize encodes a transcriptional activator of the b-ZIP class. We have isolated and characterized a gene from sorghum, related in sequence to the O2 gene from maize. A single copy of the gene is present in sorghum. Both genomic and cDNA sequences of the O2-related sorghum gene were determined. The sequence is highly homologous to maize O2 both in the promoter and in the coding region. The most closely related sequences contain the b-ZIP domain with only 11 amino acid substitutions in a total of 122 residues. In transient expression assays, the sorghum O2-related coding sequence, expressed from a CaMV 35S promoter, activates expression from the maize b-32 promoter as effectively as that obtained with the maize O2 sequence.
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    URL: http://dx.doi.org/10.1007/BF00024119
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    Cloning of two gibberellin-regulated cDNAs from Arabidopsis thaliana by subtractive hybridization: expression of the tonoplast water channel, γ-TIP, is increased by GA3 (1994)
    Springer
    Plant molecular biology 24 (1994), S. 603-615 
    Details
    ISSN: 1573-5028
    Keywords: Arabidopsis thaliana ; dwarf mutant ; gene expression ; gibberellin ; subtractive hybridization ; tonoplast intrinsic protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The Arabidopsis ga1 mutant has very low levels of endogenous, active gibberellins and thus has an extreme dwarf phenotype; application of GA3 induces stem elongation and flower development. To test the hypothesis that GA action in this system involves changes in gene expression, we have cloned mRNAs whose abundance changes following GA application. A subtraction cloning scheme for the isolation of differentially regulated cDNAs was established, involving hybridization of single-stranded cDNA to biotinylated mRNA. cDNA populations enriched up to 150-fold in GA-regulated sequences were produced and cDNA libraries generated. Screening of these libraries has isolated two clones that identify mRNAs of ca. 1100 and 750 bases whose abundance is markedly increased 24 h after GA application. One of these clones encodes the vegetative form of the Arabidopsis tonoplast intrinsic protein (γ-TIP), a water channel protein, the expression of which has recently been shown to be correlated with regions of cell expansion. The second clone is expressed only in the inflorescence and encodes a proline- and glycine-rich protein that may be a cell wall component.
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    URL: http://dx.doi.org/10.1007/BF00023557
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    A phenylalanine ammonia-lyase gene from melon fruit: cDNA cloning, sequence and expression in response to development and wounding (1994)
    Springer
    Plant molecular biology 26 (1994), S. 473-479 
    Details
    ISSN: 1573-5028
    Keywords: Cucumis melo ; melon ; phenylalanine ammonia-lyase ; gene expression ; ripening ; wounding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Phenylalanine ammonia-lyase (PAL) is the first enzyme of phenylpropanoid biosynthesis involved in the synthesis of a multiplicity of plant natural products. We have isolated and characterized a nearly fulllength cDNA clone (pmPAL-1) corresponding to a melon fruit (Cucumis melo L. var. reticulatus) gene coding for a protein which is highly similar to PAL from other lants. Melon fruit PAL is transcriptionally induced both in response to fruit ripening and wounding. PAL gene expression follows the kinetics of expression of the ethylene biosynthetic genes during fruit development. In contrast, ethylene biosynthetic genes show different induction kinetics compared to PAL expression in response to wounding. Similar results have been found for two other genes coding for enzymes involved in flavonoid biosynthesis (chalcone synthase, CHS; chalcone isomerase, CHI). Our results imply that regulation of defense gene expression in melon is a co-ordinated process in response to both ethylene and an ethylene-independent wound signal.
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    URL: http://dx.doi.org/10.1007/BF00039557
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    Regulation of an Arabidopsis oleosin gene promoter in transgenic Brassica napus (1994)
    Springer
    Plant molecular biology 25 (1994), S. 193-205 
    Details
    ISSN: 1573-5028
    Keywords: Arabidopsis ; embryo ; gene expression ; oleosin ; promoter
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Progressive deletions of the 5′-flanking sequences of an Arabidopsis oleosin gene were fused to β-glucuronidase (GUS) and introduced into Brassica napus plants using Agrobacterium-mediated transformation. The effect of these deletions on the quantitative level of gene expression, organ specificity and developmental regulation was assessed. In addition, the influence of abscisic acid (ABA), jasmonic acid (JA), sorbitol and a combined ABA/sorbitol treatment on gene expression was investigated. Sequences that positively regulate quantitative levels of gene expression are present between −1100 to −600 and −400 to −200 of the promoter. In addition, sequences present between −600 and −400 down-regulate quantitative levels of expression. In transgenic B. napus plants, the oleosin promoter directs seed-specific expression of GUS which is present at early stages of seed development and increases throughout seed maturation. Sequences present between −2500 and −1100 of the promoter are involved in modulating the levels of expression at early stages of embryo development. Histochemical staining of embryos demonstrated that expression is uniform throughout the tissues of the embryo. Sequences involved in the response to ABA and sorbitol are present between −400 and −200. The induction of GUS activity by a combined ABA/sorbitol treatment is additive suggesting that ABA is not the sole mediator of osmotically induced oleosin gene expression. A response to JA was only observed when the oleosin promoter was truncated to −600 suggesting that the reported effect of JA on oleosin gene expression may be at a post-transcriptional level.
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    URL: http://dx.doi.org/10.1007/BF00023237
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    Characterization of a cDNA from Arabidopsis thaliana encoding a potential thiol protease whose expression is induced independently by wilting and abscisic acid (1994)
    Springer
    Plant molecular biology 25 (1994), S. 259-270 
    Details
    ISSN: 1573-5028
    Keywords: abscisic acid ; Arabidopsis thaliana ; gene expression ; mutants ; signal transduction ; stress ; thiol protease ; wilting
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The sequence and expression characteristics are described of a wilt-inducible gene in Arabidopsis thaliana. A 1494 encodes a potential thiol protease whose mRNA accumulates rapidly in shoot tissue upon the loss of turgor. A1494 mRNA levels peaked after ca. 4 h and declined thereafter. Dehydration also induced rapid biosynthesis of the phytohormone abscisic acid (ABA), which continued for at least 9 h. Exogenous ABA induced the accumulation of A1494 mRNA, with kinetics similar to those after wilting. Rehydration of wilted shoots led to a rapid decline in the content of both ABA and A1494 mRNA. Wilting and ABA independently induced A1494 expression as evidenced by the effects of ABA and wilting on the ABA-deficient aba-1 and ABA-insensitive abi-1 and abi-3 genotypes. A1494 mRNA was not detectable in aba-1 shoots but accumulated rapidly after either wilting or ABA treatment, whereas the shoot ABA content was increased only by ABA treatment. ABA had no effect on A1494 mRNA levels in the abi-1 and abi-3 mutants but wilting did result in enhanced A1494 expression. Heat shock had only a minor effect on A1494 mRNA levels, whereas exposure to low temperature resulted in substantial accumulation of A1494 mRNA in wild-type shoots. However, this latter response, unlike that to drought, was mediated exclusively via ABA synthesis as demonstrated by the lack of A1494 mRNA accumulation in cold-treated aba-1 shoots.
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    Tissue-specific expression of the large ATP synthase gene cluster in spinach plastids (1994)
    Springer
    Plant molecular biology 25 (1994), S. 369-376 
    Details
    ISSN: 1573-5028
    Keywords: ATP synthase ; chloroplast ; gene expression ; plastid ; RNA stability ; transcription
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Plastids present in different tissues may vary morphologically and functionally, despite the fact that all plastids within the same plant contain identical genomes. This is achieved by regulation of expression of the plastid genome by tissue-specific factors, the mechanisms of which are not fully understood. The proton translocating ATP synthase/ATPase is a multisubunit complex composed of nine subunits, six encoded in the plastid and three in the nucleus. We have investigated the tissue-specific expression of the large ATP synthase gene cluster in spinach (Spinacia oleracea). This gene cluster encodes four of the six plastid-encoded ATP synthase genes. Transcript abundance, transcriptional activity, and transcript stability were investigated relative to gene dosage in root plastids and in stem, leaf, and flower chloroplasts. All three of these factors display significant tissue-specific variation. It was intriguing to discover that, although transcript abundance normalized to gene dosage varies in each tissue, transcript abundance as a proportion of the entire plastid RNA population in each tissue is not significantly different. Thus it appears that in these tissues the variation in transcription and stability of transcripts derived from the large ATP synthase gene cluster balances to yield an equivalent proportion of these transcripts in the plastid RNA population. Expression of this gene cluster in photosynthetic as well as non-photosynthetic tissues may facilitate the plasticity of structure and function which is characteristic of plastids.
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    URL: http://dx.doi.org/10.1007/BF00043866
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    The Chlorella virus adenine methyltransferase gene promoter is a strong promoter in plants (1994)
    Springer
    Plant molecular biology 26 (1994), S. 85-93 
    Details
    ISSN: 1573-5028
    Keywords: gene expression ; monocot cells ; promoter strength ; transient expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An upstream region isolated from a eukaryotic algal virus adenine methyltransferase gene was tested for promoter function in plants. Fusion of this region to the chloramphenicol acetyltransferase reporter gene resulted in significantly higher expression than fusion with the cauliflower mosaic virus 35S promoter. Strong levels of expression were also found in electroporated monocot plant cells. The promoter activity in transgenic tobacco plants showed tissue-specific expression. Leaves had the highest expression followed by stems and flowers. The promoter activity was not detected in root tissue. Environmental cues, such as light, and the phytohormones auxin and cytokinines had no effect on the promoter's expression. This promoter might be utilized to achieve high levels of expression of introduced genes in higher plants.
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    URL: http://dx.doi.org/10.1007/BF00039522
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    Meristem-specific gene expression directed by the promoter of the S-phase-specific gene, cyc07, in transgenic Arabidopsis (1994)
    Springer
    Plant molecular biology 24 (1994), S. 863-878 
    Details
    ISSN: 1573-5028
    Keywords: cell cycle ; gene expression ; meristem ; promoter analysis ; transgenic Arabidopsis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A genomic clone for the cyc07 gene, which is expressed specifically at the S phase during the cell cycle in synchronous cultures of periwinkle (Catharanthus roseus) cells, was isolated. Determination of the nucleotide sequence of the clone revealed that the cyc07 gene consists of seven exons separated by six introns. Genomic Southern analysis indicated that the cyc07 gene is present as a single copy per haploid genome in periwinkle. Expression of related genes was detected in a wide range of other plants. Transgenic Arabidopsis plants were generated that expressed the gene for β-glucuronidase (GUS) under the control of the promoter of the cyc07 gene. The tissue-specific pattern of expression directed by the promoter was investigated by analysis of GUS activity. Histochemical tests demonstrated that 589 bp of the 5′-upstream sequence of the cyc07 gene could direct specifical expression of the GUS reporter gene in meristematic tissues in transgenic plants. The spatial pattern of expression directed by the promoter was closely correlated with meristematic activity and cell proliferation, suggesting an association between the function of the cyc07 gene and cell proliferation.
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    Over-production of the D1 protein of photosystem II reaction centre in the cyanobacterium Synechococcus sp. PCC 7942 (1994)
    Springer
    Plant molecular biology 26 (1994), S. 709-721 
    Details
    ISSN: 1573-5028
    Keywords: gene expression ; photosynthesis ; protein turnover ; psbA ; tac promoter
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The unicellular cyanobacterium Synechococcus sp. PCC 7942 has three psbA genes encoding two different forms of the photosystem II reaction centre protein D1 (D1:1 and D1:2). The level of expression of these psbA genes and the synthesis of D1:1 and D1:2 are strongly regulated under varying light conditions. In order to better understand the regulatory mechanisms underlying these processes, we have constructed a strain of Synechococcus sp. PCC 7942 capable of over-producing psbA mRNA and D1 protein. In this study, we describe the over-expression of D1:1 using a tac-hybrid promoter in front of the psbAI gene in combination with lacI Q repressor system. Over-production of D1:1 was induced by growing cells for 12 h at 50 μmol photons m-2 s-1 in the presence of 40 or 80 μg/ml IPTG. The amount of psbAI mRNA and that of D1:1 protein in cells grown with IPTG was three times and two times higher, respectively. A higher concentration of IPTG (i.e., 150 μg/ml) did not further increase the production of the psbAI message or D1:1. The over-production of D1:1 caused a decrease in the level of D1:2 synthesised, resulting in most PSII reaction centres containing D1:1. However, the over-production of D1:1 had no effect on the pigment composition (chlorophyll a or phycocyanin/number of cells) or the light-saturated rate of photosynthesis. This and the fact that the total amounts of D1 and D2 proteins were not affected by IPTG suggest that the number of PSII centres within the membranes remained unchanged. From these results, we conclude that expression of psbAI can be regulated by using the tac promoter and lacI Q system. However, the accumulation of D1:1 protein into the membrane is regulated by the number of PSII centres.
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    URL: http://dx.doi.org/10.1007/BF00013756
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    Environmental stress-mediated differential 3′ end formation of chloroplast RNA-binding protein transcripts (1994)
    Springer
    Plant molecular biology 26 (1994), S. 833-849 
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    ISSN: 1573-5028
    Keywords: gene expression ; RNA stability regulation ; chloroplast RNA-binding protein (cRBP) ; environmental stress ; Mesembryanthemum crystallinum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We report the characterization of transcripts from the halophyte, Mesembryanthemum crystallinum, encoding a protein with high homology to chloroplast RNA-binding proteins (cRBP). In this plant chloroplast-related functions are largely protected against salt stress. cRBP transcripts are derived from a single gene, Mc32crbp, although three size classes of polyadenylated mRNAs are detected. Transcription rate and steady state amounts of mRNA are developmentally regulated and light controlled with strong transcriptional activity as functional chloroplasts are established, and with lower maintenance activity thereafter. Upon salt stress, the rate of transcription decreases, although transcript levels increase. Accompanying stress, a change in the distribution of transcript size classes is observed as the longest transcript with an untranslated 3′ end of 381 nucleotides increases relative to transcripts with shorter 3′ ends. The long transcript is characterized by the presence of five sequence elements in the 3′-untranslated region that are present in cRBP mRNAs from a variety of plants, although not all elements are found in each mRNA. The results may indicate a mechanism by which mRNA levels of constitutively light-regulated genes may be modulated without enhanced transcription in response to environmental cues.
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    URL: http://dx.doi.org/10.1007/BF00028852
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    Expression of engineered antibodies in plant cells (1994)
    Springer
    Plant molecular biology 26 (1994), S. 1023-1030 
    Details
    ISSN: 1573-5028
    Keywords: immunoglobulin genes ; gene expression ; transgenic plants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
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    URL: http://dx.doi.org/10.1007/BF00040685
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    A method for examining expression of homologous genes in plant polyploids (1994)
    Springer
    Plant molecular biology 26 (1994), S. 1065-1071 
    Details
    ISSN: 1573-5028
    Keywords: Brassica ; polyploid ; gene expression ; RT-PCR ; RFLP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract One of the essential issues regarding evolution of polyploid species is how duplicate genes are expressed. Most studies on gene expression in polyploids have been based on isozyme analyses; RNA analysis has not been widely used partially due to difficulties in distinguishing homologous transcripts which usually have the same length and similar or almost identical sequences. In this study, a method combining RT-PCR with RFLP was used to analyze transcripts of homologous genes in natural and synthetic Brassica amphidiploids. Sequences coding for several known genes were selected and used to synthesize gene-specific primers. Total RNAs were used as templates for RT-PCR to amplify homologous transcripts in three diploid parental species, three cultivated amphidiploid species and six synthetic amphidiploids. For each gene, initial PCR products amplified in all species had identical length; however, homologous transcripts in the diploid and amphidiploid species could be distinguished after digesting the PCR products with restriction enzymes. Preliminary results based on three genes indicated that both transcripts from the diploid parents were expressed in the synthetic and natural amphidiploids. This study represents the first application of RT-PCR and RFLP analysis to investigate expression of homologous genes in higher plants. The technique is a sensitive, simple and efficient method for distinguishing homologous transcripts in a mixed RNA population and can be applied to many types of studies on expression of homologous genes.
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    URL: http://dx.doi.org/10.1007/BF00040689
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    Molecular cloning of the Arabidopsis thaliana sedoheptulose-1,7-biphosphatase gene and expression studies in wheat and Arabidopsis thaliana (1994)
    Springer
    Plant molecular biology 26 (1994), S. 1191-1200 
    Details
    ISSN: 1573-5028
    Keywords: Calvin cycle genes ; gene expression ; SBPase ; Triticum aestivum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We report here the isolation and nucleotide sequence of genomic clones encoding the chloroplast enzyme sedoheptulose-1,7-bisphosphatase (SBPase) from Arabidopsis thaliana. The coding region of this gene contains eight exons (72–76 bp) and seven introns (75–91 bp) and encodes a polypeptide of 393 amino acids. Unusually, the 5′ non-coding region contains two additional AUG codons upstream of the translation initiation codon. A comparison of the deduced Arabidopsis and wheat SBPase polypeptide sequences reveals 78.6%, identity. Expression studies showed that the level of SBPase mRNA in Arabidopsis and wheat is regulated in a light-dependent manner and is also influenced by the developmental stage of the leaf. Although the Arabidopsis SBPase gene is present in a single copy, two hybridizing transcripts were detected in some tissues, suggesting the presence of alternate transcription start sites in the upstream region.
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    URL: http://dx.doi.org/10.1007/BF00040699
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    The amino acid sequence and reactive site of a single-headed trypsin inhibitor from wheat endosperm (1994)
    Springer
    The protein journal 13 (1994), S. 187-194 
    Details
    ISSN: 1573-4943
    Keywords: Trypsin inhibitor ; wheat ; primary structure ; reactive site ; Bowman-Birk
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The sequence of a trypsin inhibitor, isolated from wheat endosperm, is reported. The primary structure was obtained by automatic sequence analysis of the S-alkylated protein and of purified peptides derived from chemical cleavage by cyanogen bromide and digestion withStaphylococcus aureus V8 protease. This protein, named wheat trypsin inhibitor (WTI), which is comprised of a total of 71 amino acid residues, has 12 cysteines, all involved in disulfide bridges. The primary site of interaction (reactive site) with bovine trypsin has been identified as the dipeptide arginyl-methionyl at positions 19 and 20. WTI has a high degree of sequence identity with a number of serine proteinase inhibitors isolated from both cereal and leguminous plants. On the basis of the findings presented, this protein has been classified as a single-headed trypsin inhibitor of Bowman-Birk type.
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    URL: http://dx.doi.org/10.1007/BF01891977
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    Expression of the tobacco Tnt1 retrotransposon promoter in heterologous species (1994)
    Springer
    Plant molecular biology 26 (1994), S. 393-402 
    Details
    ISSN: 1573-5028
    Keywords: Arabidopsis thaliana ; Brassica napus ; gene expression ; Nicotiana tabacum ; retrotransposon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The expression of the tobacco (Nicotiana tabacum) retrotransposon Tntl has previously been shown to be strongly regulated and driven from the 5′ long terminal repeat (LTR). We report here that the Tntl LTR can promote activity of the β-glucuronidase (GUS) reporter gene in two heterologous species of the Brassicaceae family, namely rapessed (Brassica napus) and Arabidopsis thaliana. The translational LTR-GUS fusion was active in transient expression studies performed with tobacco and rapeseed protoplasts, indicating that the LTR sequences are recognized in heterologous species. Our results also showed that Tntl LTR-promoted GUS expression in transgenic Arabidopsis is strongly regulated, and that, in contrast to tobacco, hormonal activation plays a significant role in the expression of the Tntl LTR in Arabidopsis. LTR sequences were shown to be more effective than the CaMV 35S enhancer region in transient expression studies performed with tobacco or rapessed protoplasts; and substitution of the LTR sequences upstream from the major transcriptional start with the CaMV 35S enhancer region gave high levels of expression in transgenic tobacco and Arabidopsis leaves, suggesting that a Tntl element with similar substitutions in its 5′ LTR might be suited for gene-tagging experiments in heterologous species.
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    URL: http://dx.doi.org/10.1007/BF00039548
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    A chimeric gene (orf256) is expressed as protein only in cytoplasmic male-sterile lines of wheat (1994)
    Springer
    Plant molecular biology 26 (1994), S. 535-539 
    Details
    ISSN: 1573-5028
    Keywords: cytoplasmic male sterility ; coxI ; mitochondria ; membrane protein ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Mitochondria derived from Triticum timopheevi have a chimeric gene, orf256, immediately upstream from coxI. Antibodies to a peptide corresponding to a part of the encoded amino acid sequence of orf256 detect a 7 kDa protein on western blots of mitochondrial proteins from cytoplasmic male-sterile (cms) wheat (T. aestivum nucleus, T. timopheevi mitochondria) but not in mitochondrial proteins from T. aestivum, T. timopheevi, or cms plants restored to fertility by introduction of nuclear genes for fertility restoration. The 7 kDa protein appears to serve as a marker for cms wheat. Its occurrence as an integral protein of the inner membrane may indicate a cms effect through an influence on mitochondrial membrane function.
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    URL: http://dx.doi.org/10.1007/BF00039566
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    Structure and promoter analysis of an ABA- and stress-regulated barley gene, HVA1 (1994)
    Springer
    Plant molecular biology 26 (1994), S. 617-630 
    Details
    ISSN: 1573-5028
    Keywords: ABA ; barley ; gene expression ; Hordeum vulgare ; phylogeny ; stress
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A single-copy barley gene, HVA1, encoding a class 3 late embryogenesis-abundant protein, can be induced by either treatment with abscisic acid (ABA) or by stress conditions such as drought, cold, heat and salinity. We have isolated an HVA1 genomic clone containing about 400 bp of 5′-upstream sequence, a single 109 bp intron, and the full coding sequence. Linker scan mutagenesis and transient expression studies were used to test the function of four HVA1 promoter elements conserved in ABA-responsive genes. Mutations in two of these elements, the C box and the putative ABRE 1 (ABA-responsive element) containing an ACGT core, resulted in no significant change in transcription level or ABA induction. In contrast, mutations of the other two elements, putative ABRE 2 & 3 cause the level of transcription to drop to 10–20% of that obtained with the wild-type promoter indicating that the high level of expression of HVA1 is dependent on both pABRE 2 & 3. Interestingly, despite their low level of expression, the mutated promoters still gave more than 20-fold induction in response to ABA treatment. We suggest that the ABA induction of barley HVA1 gene is governed by a complex consisting of pABRE 2 & 3 working together to regulate the absolute level of expression, and either of these elements or a possible third element may regulate ABA inducibility. Phylogenetic analysis by parsimony indicates that the barley HVA1 and wheat pMA2005 sequences share a recent common ancester. These two genes are closely related to the carrot Dc3 and cotton D-7 genes with which they share a similar structural gene organization.
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    Detection of immunologically related Kunitz and Bowman-Birk proteinase inhibitors expressed during potato tuber development (1994)
    Springer
    Plant molecular biology 26 (1994), S. 961-969 
    Details
    ISSN: 1573-5028
    Keywords: gene expression ; Kunitz-type proteinase inhibitor ; potato (Solanum tuberosum, L.) ; soybean C-II inhibitor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Antiserum against a potato Kunitz-type proteinase inhibitor (PKPI) expressed in Escherichia coli was produced. In immunoblotting assays of proteins from potato tubers cultured in vitro, three proteins reacted to the antiserum, two of 20 kDa and one of 10 kDa. Their N-termini were sequenced. While the 20 kDa proteins showed 59 and 90% identity to PKPI, the 10 kDa one had 65% identity to soybean C-II proteinase inhibitor. Characterization of the temporal expression of these proteins showed that both could be detected from 10 days after induction of tuberization (DAI) in vitro, but the times when maximum amounts of PKPI and 10 kDa protein could be detected were different, corresponding to 22 and 32 DAI, respectively. The amounts of these proteins decreased in the following stages, and no positive reaction of the antiserum with mature tuber proteins could be found. The 20 kDa proteins were also detected in early stages of development of potato tubers grown in the field, indicating that these proteins are expressed during normal tuber development, and differ from the PKPIs reported previously.
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    Sharp divergence between wheat and barley at loci encoding novel members of the trypsin/α-amylase inhibitors family (1994)
    Springer
    Plant molecular biology 26 (1994), S. 1231-1236 
    Details
    ISSN: 1573-5028
    Keywords: chromosome mapping ; inhibitors of trypsin/α-amylases ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Amino acid sequences for three members (CMx1, CMx2, and CMx3) of a new subfamily of trypsin/α-amylase inhibitors in wheat have been deduced from the nucleotide sequences of the corresponding cDNAs. A cDNA clone encoding CMx1 was selected from a wheat developing endosperm library using a probe that encoded barley trypsin inhibitor BTI-CMe at low stringency. Sequences corresponding to CMx2 and CMx3 were obtained from cDNA amplified by the polymerase chain reaction. The three CMx sequences contain a premature stop codon after 363 nt, as well as a second stop codon at the same position as in BTI-CMe (nt 439–441). Southern analysis of DNAs from diploid, tetraploid, and hexaploid wheats, as well as from aneuploid lines, indicate that there is a single CMx locus in each of the three genomes of hexaploid wheat, respectively associated with chromosomal arms 4AS, 4BS, and 4DL. These genes are expressed early during endosperm development and not expressed at detectable levels in other tissues. Evolutionary implications are discussed.
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    Cloning and molecular analysis of structural genes involved in flavonoid and stilbene biosynthesis in grape (Vitis vinifera L.) (1994)
    Springer
    Plant molecular biology 24 (1994), S. 743-755 
    Details
    ISSN: 1573-5028
    Keywords: anthocyanins ; cDNA cloning ; flavonoids ; gene expression ; genomic organization ; stilbenes ; Vitis vinifera L
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Genes involved in flavonoid and stilbene biosynthesis were isolated from grape (Vitis vinifera L.). Clones coding for phenylalanine ammonia-lyase (PAL), chalcone synthase (CHS), chalcone isomerase (CHI), flavanone 3-hydoxylase (F3H), dihydroflavonol 4-reductase (DFR), leucoanthocyanidin dioxygenase (LDOX) and UDP glucose:flavonoid 3-O-glucosyl transferase (UFGT), were isolated by screening a cDNA library, obtained from mRNA from seedlings grown in light for 48 h using snapdragon (Antirrhinum majus) and maize heterologous probes. A cDNA clone coding for stilbene synthase (StSy) was isolated by probing the library with a specific oligonucleotide. These clones were sequenced and when the putative products were compared to the published amino acid sequence for corresponding enzymes, the percentages of similarity ranged from 65% (UFGT) to 90% (CHS and PAL). The analysis of the genomic organization and expression of these genes in response to light shows that PAL and StSy genes belong to large multigene families, while the others are present in one to four copies per haploid genome. The steady-state level of mRNAs encoded by the flavonoid biosynthetic genes as determined in young seedlings is coordinately induced by light, except for PAL and StSy, which appear to be constitutively expressed.
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    A ribosomal protein S10 gene is found in the mitochondrial genome in Solanum tuberosum (1994)
    Springer
    Plant molecular biology 25 (1994), S. 743-749 
    Details
    ISSN: 1573-5028
    Keywords: apocytochrome b pseudogene ; pea cox1 ; plant mitochondria ; potato ; S10 ribosomal protein ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The S10 ribosomal protein gene (rps10), which has not been previously reported in any angiosperm mitochondrial genome, was identified by sequence analysis in the potato mitochondrial DNA. This gene is found downstream of a truncated non-functional apocytochrome b (cob) pseudogene, and is expressed as multiple transcripts ranging in size from 0.8 to 5.0 kb. Southern hybridization analysis indicates that rps10-homologous sequences are not present in the wheat mitochondrial genome. Sequence analysis of a single-copy region of the pea mitochondrial genome located upstream of cox1 [11] shows that a non-functional rps10 pseudogene is present in this species. These results suggest that the functional genes coding for wheat and pea mitochondrial RPS10 polypeptides have been translocated to the nucleus.
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    Triticum aestivum puroindolines, two basic cystine-rich seed proteins: cDNA sequence analysis and developmental gene expression (1994)
    Springer
    Plant molecular biology 25 (1994), S. 43-57 
    Details
    ISSN: 1573-5028
    Keywords: cDNA sequence ; cystine-rich proteins ; gene expression ; puroindolines ; tryptophan-rich domain ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract From a mid-maturation seed cDNA library we have isolated cDNA clones encoding two Triticum aestivum puroindolines. Puroindoline-a and puroindoline-b, which are 55% similar, are basic, cystine-rich and tryptophan-rich proteins. Puroindolines are synthezised as preproproteins which include N- and C-terminal propeptides which could be involved in their vacuolar localization. The mature proteins have a molecular mass of 13 kDa and a calculated isoelectric point greater than 10. A notable feature of the primary structure of puroindolines is the presence of a tryptophan-rich domain which also contains basic residues. A similar tryptophan-rich domain was found within an oat seed protein and a mammalian antimicrobial peptide. The ten cysteine residues of puroindolines are organized in a cysteine skeleton which shows similarity to the cysteine skeleton of other wheat seed cystine-rich proteins. Northern blot analysis showed that puroindoline genes are specifically expressed in T. aestivum developing seeds. No puroindoline transcripts as well as no related genes were detected in Triticum durum. The identity of puroindolines to wheat starch-granule associated proteins is discussed as well as the potential role of puroindolines in the plant defence mechanism.
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    URL: http://dx.doi.org/10.1007/BF00024197
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    Structure of genes that encode isozymes of aspartate aminotransferase in Panicum miliaceum L., a C4 plant (1994)
    Springer
    Plant molecular biology 26 (1994), S. 723-734 
    Details
    ISSN: 1573-5028
    Keywords: aspartate aminotransferase ; C4 photosynthesis ; gene expression ; gene structure ; isozyme
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The cytosolic and mitochondrial isozymes of aspartate aminotransferase (AspAT) function in the C4 photosynthetic cycle in NAD-malic enzyme-type C4 plants and are expressed at high levels in mesophyll cells and bundle sheath cells, respectively. We constructed a genomic library from Panicum miliaceum, a NAD-malic enzyme-type C4 plant, and cloned the genes for these isozymes. The sequence of the cloned gene for cytosolic AspAT spans 7800 bp and consists of 12 exons. The sequence of the cloned gene for mitochondrial AspAT spans 9000 bp and consists of 10 exons. The results of primer-extension analysis suggest that transcription may be initiated from multiple adjacent sites. Both genes have significant GC-rich regions around the site of initiation of transcription, and these regions showed no CpG suppression. The 5′-flanking regions of both genes include several short sequences similar to the regulatory elements found in other genes for components of the photosynthetic machinery. In particular, the cytosolic AspAT gene contains sequences similar to nuclear protein-binding sites in other mesophyll-expressed C4 photosynthetic genes and the mitochondrial AspAT gene contains elements for light-sensitive and constitutive expression of a bundle sheath-expressed gene. The results of Southern analysis indicated that there are at least two genes that encode each isozyme in the genome of P. miliaceum. A comparison of nitron-insertion positions between AspAT genes of plants and animals revealed that several introns are located at identical positions. On the basis of a phylogenetic tree among AspATs and tyrosine aminotransferase, we have shown that the introns of aminotransferase genes antedate the divergence of eubacteria, archaebacteria, and eukaryotes.
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    Vascular expression of the grp1.8 promoter is controlled by three specific regulatory elements and one unspecific activating sequence (1994)
    Springer
    Plant molecular biology 26 (1994), S. 747-756 
    Details
    ISSN: 1573-5028
    Keywords: activating sequence ; gene expression ; glycine-rich protein ; tobacco ; vascular expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The bean grp1.8 full-length promoter is specifically active in vascular tissue during normal development of tobacco. Deletion of a negative regulatory element resulted in ectopic activity of the promoter in cortical cells of hypocotyls, roots and stems. A 169 bp fragment (−205 to −36) of the grp1.8 promoter conferred vascular-specific expression to CaMV 35S minimal promoters whereas a 141 bp fragment (−205 to −64) strongly activated these minimal promoters both in vascular and cortical cells. These experiments defined a new regulatory element (VSE) that is essential for vascular-specific expression and is located between −64 and −36. The 141 bp grp1.8 promoter sequence had enhancer-like properties as it was active in both orientations. A 24 bp sequence (bp −119 to −96, corresponding to the SE1 regulatory element) enhanced expression from several minimal promoters strongly but unspecifically, whereas a 26 bp sequence (−98 to −73, corresponding to the RSE regulatory element) induced vascular-specific expression. Thus, the grp1.8 promoter is regulated by a combinatorial mechanism that can integrate the action of different, non-additively acting regulatory elements into vascular-specific expression.
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    URL: http://dx.doi.org/10.1007/BF00013759
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    A dehydrin cognate protein from pea (Pisum sativum L.) with an atypical pattern of expression (1994)
    Springer
    Plant molecular biology 26 (1994), S. 805-816 
    Details
    ISSN: 1573-5028
    Keywords: Dehydrin ; gene expression ; pea (Pisum sativum L.) ; cognate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Dehydrins are a family of proteins characterised by conserved amino acid motifs, and induced in plants by dehydration or treatment with ABA. An antiserum was raised against a synthetic oligopeptide based on the most highly conserved dehydrin amino acid motif, the lysine-rich block (core sequence KIKEK-LPG). This antiserum detected a novel M r 40 000 polypeptide and enabled isolation of a corresponding cDNA clone, pPsB61 (B61). The deduced amino acid sequence contained two lysine-rich blocks, however the remainder of the sequence differed markedly from other pea dehydrins. Surprisingly, the sequence contained a stretch of serine residues, a characteristic common to dehydrins from many plant species but which is missing in pea dehydrin. The expression patterns of B61 mRNA and polypeptide were distinctively different from those of the pea dehydrins during seed development, germination and in young seedlings exposed to dehydration stress or treated with ABA. In particular, dehydration stress led to slightly reduced levels of B61 RNA, and ABA application to young seedlings had no marked effect on its abundance. The M r 40 000 polypeptide is thus related to pea dehydrin by the presence of the most highly conserved amino acid sequence motifs, but lacks the characteristic expression pattern of dehydrin. By analogy with heat shock cognate proteins we refer to this protein as a dehydrin cognate.
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    Gibberellins: perception, transduction and responses (1994)
    Springer
    Plant molecular biology 26 (1994), S. 1529-1555 
    Details
    ISSN: 1573-5028
    Keywords: gibberellin ; growth ; development ; perception ; receptor ; gene expression ; signal transduction ; response mutant ; calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
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    URL: http://dx.doi.org/10.1007/BF00016489
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    Isolation and characterization of two β-tubulin cDNA clones from rice (1994)
    Springer
    Plant molecular biology 26 (1994), S. 1975-1979 
    Details
    ISSN: 1573-5028
    Keywords: β-tubulin ; cDNA ; rice ; monocot ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two cDNA clones encoding two different β-tubulins, RTUB-1 and RTUB-2, were isolated from a rice cDNA library and their nucleotide sequences were analyzed. The deduced amino acid sequences showed amino acid sequence identity between 92% and 97% with other plant β-tubulins. Southern blot analysis using gene-specific and coding-region probes suggested that β-tubulins in rice are encoded by multigene families. The two cDNA clones represent two subfamilies of rice tubulins. RTUB-1 and RTUB-2, consisting of 3 to 4 genes and a single gene, respectively. The transcript levels of RTUB-1 and RTUB-2 genes were higher in actively elongating tissues such as etiolated shoot tissues and light-grown root tissues of four-day old seedlings.
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    Changes in polypeptide patterns in tobacco roots colonized by two Glomus species (1994)
    Springer
    Mycorrhiza 4 (1994), S. 215-221 
    Details
    ISSN: 1432-1890
    Keywords: Nicotiana ; Glomus species ; arbuscular mycorrhiza ; gene expression ; specific polypeptides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Changes in gene expression were studied during the establishment of arbuscular mycorrhizal symbiosis in tobacco roots from an amphidiploid hybrid Nicotiana glutinosa x N. debneyi. Polypeptide patterns from control roots and from roots infected by Glomus mosseae or G. intraradices were resolved by two-dimensional polyacrylamide gel electrophoresis and followed in a time-course analysis. Arbuscular mycorrhizal infection led to significant modifications in polypeptide patterns with: (a) decreased amounts of some polypeptides, (b) increased accumulation of others, and (c) appearance of newly-induced polypeptides. Comparisons made during infection development by the two Glomus species demonstrated that protein modifications changed in relation to the mycorrhizal state of the tobacco roots.
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    Tissue specific expression of an α-skeletal actin-lacZ fusion gene during development in transgenic mice (1994)
    Springer
    Transgenic research 3 (1994), S. 59-66 
    Details
    ISSN: 1573-9368
    Keywords: α-actin ; transgenic mice ; gene expression ; muscle ; embryos ; lacZ
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Transgenic mice carrying a chimaeric transgene containing 730 bp of the 5′-flanking sequences and the entire first intron of the rat α-skeletal actin gene fused to thelacZ reporter gene have been produced by microinjection. ThelacZ reporter gene was used to verify the suitability of using the rat α-actin promoter elements to target expression of genes of agricultural and therapeutic value exclusively to skeletal and heart muscle cells and fibres of transgenic mice. Expression of the transgene indicates a tightly regulated developmental and muscle specific control of the rat α-skeletal actin gene, making it a useful promoter for gene targeting to muscle tissues. The cells destined to form muscle tissues in these transgenic mice are readily visualized in intact embryos by staining for β-galactosidase activity, making them a suitable animal model for studying the origin and development of skeletal and cardiac muscle tissues.
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    Complementation of an alcohol dehydrogenase-deficientNicotiana plumbaginifolia mutant by transformation with theArabidopsis thaliana Adh gene (1994)
    Springer
    Transgenic research 3 (1994), S. 376-387 
    Details
    ISSN: 1573-9368
    Keywords: alcohol dehydrogenase ; Arabidopsis thaliana ; functional complementation ; gene expression ; Nicotiana plumbaginifolia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An alcohol dehydrogenase-deficient (ADH) mutant ofNicotiana plumbaginifolia, selected on the basis of ethanol resistance, was restored for ADH activity by transformation with anAdh gene fromArabidopsis thaliana expressed under the control of its own promoter or the CaMV 35S promoter. The expression in various organs (seed, root, leaf and pollen) was analysed at the protein and RNA levels as well as byin situ detection of ADH activity. The analysis of spatial and temporal regulation of theA. thaliana Adh gene expression suggests that ADH expression is controlled at the transcriptional level.
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    Carbohydrate binding activities ofBradyrhizobium japonicum: IV. Effect of lactose and flavones on the expression of the lectin, BJ38 (1994)
    Springer
    Glycoconjugate journal 11 (1994), S. 363-370 
    Details
    ISSN: 1573-4986
    Keywords: lectin ; gene expression ; cell-cell adhesion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract BJ38 is a galactose/lactose-specific lectin (M r ∼ 38000) found at one pole ofBradyrhizobium japonicum. It has been implicated in mediating the adhesion of the bacteria to soybean roots, leading to the establishment of a nitrogen-fixing symbiosis. When the ligand lactose is added to cultures of the bacteria for at least 1 h prior to harvesting the cells for BJ38 isolation, the yield of the protein was found to be elevated in a dose-dependent fashion. Half maximal stimulation was observed at ∼ 50 µm; the effect was saturated at ∼ 1mm, where a 10-fold higher yield of BJ38 was obtained. Saccharides with a lower affinity for BJ38 than lactose yielded a correspondingly smaller induction effect when compared at a concentration of 1mm. The higher level of BJ38 induced by lactose is also manifested by an elevated amount of BJ38 detectable at the cell surface and by a higher number ofB. japonicum cells adsorbed onto soybean cells. Surprisingly, the induction of BJ38 expression seen with lactose was also observed with certain, but not all, flavonoids that induce thenod genes of the bacteria; genistein mimicked the induction observed with lactose, whereas luteolin failed to stimulate BJ38 production.
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    URL: http://dx.doi.org/10.1007/BF00731210
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    Recombinant protein expression in aDrosophila cell line: comparison with the baculovirus system (1994)
    Springer
    Cytotechnology 15 (1994), S. 139-144 
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    ISSN: 1573-0778
    Keywords: Baculovirus ; cell culture ; Drosophila ; gene expression ; insect cell ; metallothionein promoter ; recombinant protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract In this report, we compare two different expression systems: baculovirus/Sf9 and stable recombinantDrosophila Schneider 2 (S2) cell lines. The construction of a recombinant S2 cell line is simple and quick, and in batch fermentations the cells have a doubling time of 20 hours until reaching a plateau density of 20 million cells/ml. Protein expression is driven by theDrosophila Metallothionein promoter which is tightly regulated. When expressed in S2 cells, the extracellular domain of human VCAM, an adhesion molecule, is indistinguishable from the same protein produced by baculovirus-infected Sf9 cells. Additionally, we present data on the expression of a seven trans-membrane protein, the dopamine D4 receptor, which has been successfully expressed in both systems. The receptor integrates correctly in the S2 membrane, binds [3H]spiperone with high affinity and exhibits pharmacological characteristics identical to that of the receptor expressed in Sf9 and mammalian cells. The general implications for large scale production of recombinant proteins are discussed.
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    URL: http://dx.doi.org/10.1007/BF00762388
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    Evaluation of various methods for the detection of barley yellow dwarf virus by the tissue-blot immunoassay and its use for virus detection in cereals inoculated at different growth stages (1994)
    Springer
    European journal of plant pathology 100 (1994), S. 71-80 
    Details
    ISSN: 1573-8469
    Keywords: wheat ; Triticum aestivum ; oat ; Avena sativa ; barley ; Hordeum vulgare ; serology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Various modifications of the tissue-blot immunoassay (TBIA) for the detection of barley yellow dwarf virus (BYDV, luteovirus) were compared. Similar results were obtained by using three different labelled molecules; goat anti-rabbit antibodies conjugated to alkaline phosphatase, protein A conjugated with alkaline phosphatase and goat anti-rabbit antibodies conjugated with colloidal gold. Blocking the nitrocellulose membrane with polyvinyl alcohol for 1 min was effective and allowed the procedure to be shortened by one hour. TBIA was sensitive enough to detect BYDV in old dry tissue wich had been soaked in water for 1 h. BYDV was monitored by TBIA in wheat, oat and barley after inoculation at heading, flowering and grain filling growth stages. The later the inoculation date, the greater the chance of detecting the virus in stem bases rather than in the upper part of the stem. The later the inoculation the less virus moved, from the inoculated tiller to other tillers of the same plant.
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    URL: http://dx.doi.org/10.1007/BF01871967
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    Extractable sulphate and organic sulphur in soils and their availability to plants (1994)
    Springer
    Plant and soil 164 (1994), S. 243-250 
    Details
    ISSN: 1573-5036
    Keywords: organic sulphur ; soil testing ; sulphate ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Ten soils collected from the major arable areas in Britain were used to assess the availability of soil sulphur (S) to spring wheat in a pot experiment. Soils were extracted with various reagents and the extractable inorganic SO4-S and total soluble S(SO4-S plus a fraction of organic S) were determined using ion chromatography (IC) or inductively-coupled plasma atomic emission spectrometry (ICP-AES), respectively. Water, 0.016 M KH2PO4, 0.01 M CaCl2 and 0.01 M Ca(H2PO4)2 extracted similar amounts of SO4-S, as measured by IC, which were consistently smaller than the total extractable S as measured by ICP-AES. The amounts of organic S extracted varied widely between different extractants, with 0.5 M NaHCO3 (pH 8.5) giving the largest amounts and 0.01 M CaCl2 the least. Organic S accounted for approximately 30–60% of total S extracted with 0.016 M KH2PO4 and the organic C:S ratios in this extract varied typically between 50 and 70. The concentrations of this S fraction decreased in all soils without added S after two months growth of spring wheat, indicating a release of organic S through mineralisation. All methods tested except 0.5 M NaHCO3-ICP-AES produced satisfactory results in the regression with plant dry matter response and S uptake in the pot experiment. In general, 0.016 M KH2PO4 appeared to be the best extractant and this extraction followed by ICP-AES determination was considered to be a good method to standardise on.
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    Biofumigation: Isothiocyanates released frombrassica roots inhibit growth of the take-all fungus (1994)
    Springer
    Plant and soil 162 (1994), S. 107-112 
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    ISSN: 1573-5036
    Keywords: canola ; glucosinolates ; Indian mustard ; take-all ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The presence of root tissue of the brassicas canola and Indian mustard inhibited growth of pure cultures of the fungal pathogen which causes take-all of wheat [Gaeumannomyces graminis (Sacc.) Arx and Oliver var.tritici, abbreviated as Ggt]. Ggt growth was generally inhibited more in the presence of Indian mustard roots than canola roots. Dried irradiated roots were consistently effective in reducing Ggt growth, but growth inhibition by young live roots and macerated roots was not consistent. The inhibitory compound(s) were shown to be volatile because the symmetry of Ggt growth was not affected by the proximity of theBrassica tissue. Volatile breakdown products from maceratedBrassica roots were identified using a gas chromatograph-mass spectrometer. The major compounds found were isothiocyanates (ITCs). Canola roots released mostly methyl ITC and Indian mustard roots released mostly phenylethyl ITC. Low concentrations of these and related compounds inhibited growth of Ggt in pure culture when supplied as the vapour of pure chemicals in concentrations within the range expected during breakdown ofBrassica roots in soil.
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    URL: http://dx.doi.org/10.1007/BF01416095
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    3Hthymidine incorporation of rhizosphere bacteria influenced by plant N-status (1994)
    Springer
    Plant and soil 162 (1994), S. 113-116 
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    ISSN: 1573-5036
    Keywords: ammonium ; nitrate ; split-roots ; root exudate ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The effect of plant-root N-status on bacterial growth in the rhizosphere was studied with 5-week-old wheat plants grown in soil with low N content obtained by mixing 9:1 gravel:sandy loam. As a consequence of N limitation, significant increase in3Hthymidine (Tdr) incorporation rate occured 3 days after addition of 30 mM ammonium compared to controls without ammonium. Plants were grown with split-roots to separate the effect of soil N from effect of plant root derived organic matter-N on bacterial activity. The increase in nitrate concentration from 10 mM to 30 mM at one part of the root system led to significant increased3HT dr incorporation in the rhizosphere at the other part of root system after 4 days showing that the composition of root exudates became more favourable for bacterial growth when plants were fertilized with the higher level of nitrate.
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    URL: http://dx.doi.org/10.1007/BF01416096
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    Growth, biomass allocation and water use efficiency of two wheat cultivars in a mediterranean environment; a pot experiment under field conditions (1994)
    Springer
    Plant and soil 162 (1994), S. 241-247 
    Details
    ISSN: 1573-5036
    Keywords: biomass allocation ; carbon isotope discrimination ; growth ; water use efficiency ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Plants of two bread wheat cultivars,Triticum aestivum L. ‘Katya Al’ and ‘Mexipak 65’, were grown in pots during the crop season in the field in NW Syria, a region with a Mediterranean climate. The experiment involved two treatments. Control plants were well-watered throughout the experiment (watering to 0.22 g water g−1 dry soil). In the second treatment, water was withheld from the plants until soil water content had decreased to 0.10 g water g−1 dry soil, the level that was maintained thereafter. Water use was measured by weighing the pots, and growth by destructive sampling. Growth of Katya and Mexipak was similar. Mexipak had a lower (though not significant atp〈0.05) plant water use efficiency (WUEp) in both treatments due to higher rates of water loss. On a leaf area basis differences in water use were especially high since Mexipak had a smaller total leaf area. In spite of a smaller investment in photosynthesizing area, Mexipak achieved similar growth as Katya. Carbon isotope discrimination and organic nitrogen concentration (both higher for Mexipak) suggest that Mexipak accomplished higher mean net photosynthetic rates with a higher mean leaf diffusive conductance, higher intercellular carbon dioxide partial pressure, and possibly a greater investment in the photosynthetic apparatus compared to Katya. Differences in carbon isotope discrimination suggest a larger difference in average photosynthetic WUE (net photosynthesis/transpiration) than in plant WUE. This could indicate that loss of carbon in respiration was greater in Katya. Gas exchange measurements on the youngest fully expanded leaves showed only minor differences between the cultivars. It is hypothesized that Mexipak, with a smaller total leaf area, is able to maintain high leaf conductance and photosynthesis for a longer period of time during the day or during the life span of leaves.
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    URL: http://dx.doi.org/10.1007/BF01347711
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    The 2,4-D-induced wheat para-nodules are modified lateral roots with structure enhanced by rhizobial inoculation (1994)
    Springer
    Plant and soil 159 (1994), S. 121-129 
    Details
    ISSN: 1573-5036
    Keywords: 2,4-dichlorophenoxyacetate ; para-nodule ; Rhizobium trifolii ; structure ; Triticum aestivum L. ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Nodular outgrowths (para-nodules or p-nodules) on the roots of wheat (Triticum aestivum L.) cv. Miskle seedlings were induced by treatment with 0.3 and 0.6mg L−1 2,4-dichlorophenoxyacetate (2,4-D). When co-inoculated with Rhizobium trifolii strain ATCC 14480, more p-nodules were formed at these levels and p-nodulation occured at 0.1 mg L−1 indicating that inoculation enhances 2,4-D-induced p-nodulation. Similar to lateral roots, the p-nodules arose from the pericycle opposite the phloem tissues and were free from the cortical cells of the parental root at all stages of development. Structurally, the p-nodules exhibited tissue differentiation. They possessed a highly organized central vascular cylinder connected to that of the parent root, an endodermis, a cap, and an apical and lateral meristems. P-nodules formed by 2,4-D treatment alone were irregularly lobed due to uncoordinated activity of the apical meristem, while those in the combined 2,4-D and inoculation treatment were more globose. The results of the present study indicate that the 2,4-D-induced wheat p-nodules are modified lateral roots, the structure of which is enhanced by rhizobial inoculation.
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    The completion of cell proliferation and growth in wheat radicle (1994)
    Springer
    Plant and soil 167 (1994), S. 43-49 
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    ISSN: 1573-5036
    Keywords: DNA contents ; DNA synthesis ; growth ; proliferation ; radicle ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The pattern of proliferation and growth of cortical and central metaxylem cells in a radicle and the transitional zone of a wheat embryo was studied during the final stages of embryogenesis. Cell divisions finished nearer the root tip in the central metaxylem than was the case in the cortex. After divisions ceased the cells of both tissues maintained the ability to synthesize DNA and the cells began DNA endoreduplication. The maximal levels of endoreduplication were 4C and 8C in cortical and central metaxylem cells, respectively. As a result of nonsimultaneous cessation of divisions, the metaxylem cells were two or three times longer than cortical cells. The proportion of cells with the maximal DNA content was smaller in the transitional zone than in the radicle. During the final embryonal stages cell growth rate was decreased. It was established that the transition of cells to DNA synthesis was inhibited in all sites of the radicle during the completion of embryogenesis. The cell growth was topped in proximal sites of the radicle. In the division zone the cells which had already begun DNA synthesis were able to complete it and divided. Cell growth stopped simultaneously with completion of proliferation in this zone.
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    Genetic basis of grain filling rate in wheat (Triticum aestivum L. emend. Thell.) (1994)
    Springer
    Euphytica 76 (1994), S. 33-44 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; genetic basis ; grain filling rate ; genetic effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Grain filling rate in wheat (Triticum aestivum L. emend. Thell.) positively influences grain yield under a wide range of conditions. The effective utilization of this trait in breeding depends on an understanding of its genetic control. A study was, therefore, conducted to determine the genetic basis of grain filling rate in six crosses of wheat. Higher order genic interactions and/or linkage were important in the genetic regulation of grain filling rate (GFR) in the majority of crosses. Additive ([d]) and dominance ([h]) gene effects were important in the control of GFR in main ears (ME) and whole plant ears (WPE). Additive and additive × additive epistatic effects were the most important in the genetic control of GFR in last ears (LE). Location effects on genetic effects for GFR were significant (P 〈 0.05) in all ear types of some crosses except in ME. Genotype × environment interaction effects were important (P 〈 0.001) in LE and WPE. It was concluded that the inheritance of GFR is complex and is dependent on ear type. Breeding procedures that facilitate the exploitation of non-additive and additive gene effects were recommended for the genetic improvement of grain filling rate of wheat.
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    Analysis of disease resistance and quality characters of F1 hybrids of crosses between wheat (Triticum aestivum) and spelt (Triticum spelta) (1994)
    Springer
    Euphytica 75 (1994), S. 105-110 
    Details
    ISSN: 1573-5060
    Keywords: wheat ; spelt ; crosses ; hybrids ; quality ; disease resistance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary With the objective of creating new combinations of disease resistance and quality, hybrids between wheat and spelt (spelt is well adapted to cool and wet conditions) were produced and the expression of heterosis was analysed. Three winter wheat varieties were crossed reciprocally with two spelt cultivars and the F1 hybrids were tested under artificial inoculation with stripe rust, powdery mildew and leaf rust. Disease susceptibility and quality characters (protein content, Zeleny value, grain hardness) were assessed in two year field trials. For stripe rust the F1 hybrids were resistant if one of the wheat parents was resistant. Combinations with the susceptible wheat cultivar ‘Arina’ were all susceptible irrespective of using a resistant spelt partner. Although the infection with powdery mildew was rather low, a similar reaction was obtained with the susceptible wheat variety ‘Bernina’. Leaf rust revealed very specific varietal influences. The two susceptible wheat varieties ‘Bernina’ and ‘Arina’ resulted in susceptible F1 hybrids when combined with a moderately resistant spelt. Only when they were crossed with a resistant spelt cultivar the F1 hybrids were resistant. ‘Forno’, a leaf rust resistant wheat, gave resistant F1 hybrids in all combinations. Without exception the quality characters tested showed a negative heterosis effect resulting in protein levels and Zeleny values close to or below the values of the lower parent. It appears to be possible to produce resistant F1 hybrids, mostly dominated by the resistance level of the wheat partner. The quality of the hybrids is mainly suitable for biscuit and spelt specific products; it needs specific screening for combinations with acceptable breadmaking quality.
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    UV-B damage and protection at the molecular level in plants (1994)
    Springer
    Photosynthesis research 39 (1994), S. 475-489 
    Details
    ISSN: 1573-5079
    Keywords: DNA repair ; flavonoids ; gene expression ; oxidative stress ; photosynthesis ; promoter
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Influx of solar UV-B radiation (280–320 nm) will probably increase in the future due to depletion of stratospheric ozone. In plants, there are several targets for the deleterious UV-B radiation, especially the chloroplast. This review summarizes the early effects and responses of low doses of UV-B at the molecular level. The DNA molecules of the plant cells are damaged by UV due to the formation of different photoproducts, such as pyrimidine dimers, which in turn can be combatted by specialized photoreactivating enzyme systems. In the chloroplast, the integrity of the thylakoid membrane seems to be much more sensitive than the activities of the photosynthetic components bound within. However, the decrease of mRNA transcripts for the photosynthetic complexes and other chloroplast proteins are among very early events of UV-B damage, as well as protein synthesis. Other genes, encoding defence-related enzymes, e.g., of the flavonoid biosynthetic pathway, are rapidly up-regulated after commencement of UV-B exposure. Some of the cis-acting nucleotide elements and trans-acting protein factors needed to regulate the UV-induced expression of the parsley chalcone synthase gene are known.
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    Acclimation of photosynthetic proteins to rising atmospheric CO2 (1994)
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    Photosynthesis research 39 (1994), S. 413-425 
    Details
    ISSN: 1573-5079
    Keywords: elevated CO2 ; gene expression ; Rubisco ; rbcL ; rbcS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In this review we discuss how the photosynthetic apparatus, particularly Rubisco, acclimates to rising atmospheric CO2 concentrations (ca). Elevated ca alters the control exerted by different enzymes of the Calvin cycle on the overall rate of photosynthetic CO2 assimilation, so altering the requirement for different functional proteins. A decreased flux of carbon through the photorespiratory pathway will decrease requirements for these enzymes. From modeling of the response of CO2 uptake (A) to intracellular CO2 concentration (ci) it is shown that the requirement for Rubisco is decreased at elevated ca, whilst that for proteins limiting ribulose 1,5 bisphosphate regeneration may be increased. This balance may be altered by other interactions, in particular plasticity of sinks for photoassimilate and nitrogen supply; hypotheses on these interactions are presented. It is speculated that increased accumulation of carbohydrate in leaves developed at elevated ca may signal the ‘down regulation’ of Rubisco. The molecular basis of this ‘down regulation’ is discussed in terms of the repression of photosynthetic gene expression by the elevated carbohydrate concentrations. This molecular model is then used to predict patterns of acclimation of perennials to long term growth in elevated ca.
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    Seedling root response of some Kenyan bread wheat cultivars grown in acid nutrient culture solution containing aluminum (1994)
    Springer
    Plant and soil 158 (1994), S. 141-144 
    Details
    ISSN: 1573-5036
    Keywords: acid tolerance ; cultivar differences ; root tolerance index ; Triticum aestivum L. ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The objective of this study was to determine whether a series of Kenyan bread wheat cultivars differed in tolerance to aluminum toxicity. Fourteen Kenyan wheat cultivars representing current and former widely grown cultivars of diverse pedigree origin, and two control cultivars, Maringa (Al-tolerant) and Siete Cerros (Al-susceptible), were tested in solution cultures with 0 (control), 148, 593, and 2370 μM Al at pH 4.6. Highly significant (p≤0.01) differences in seedling growth were observed among cultivars for root mass, root length and root tolerance index (RTI). Significant (p≤0.05) cultivar × treatment interactions were observed for root mass and RTI. All characters were negatively affected by increased Al concentration, with root length and root mass being affected the most. RTI is a commonly used index which measures the relative performance of individual cultivars with and without aluminum stress. High levels of tolerance to Al were identified in the Kenyan cultivars by evaluating RTI with this simple nutrient solution technique. Romany and Kenya Nyumbu had RTI values approaching those of the Al tolerant Brazilian cultivar Maringa, a spring wheat standard that has been used for high Al tolerance.
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    Evaluation of the use of a model rhizodeposition technique to separate root and microbial respiration in soil (1994)
    Springer
    Plant and soil 165 (1994), S. 89-101 
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    ISSN: 1573-5036
    Keywords: barley ; glucose ; microbial respiration ; pulse-labelling ; rhizodeposition ; root respiration ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A model rhizodeposition technique to estimate the root and microbial components of 14C soil/root respiration in pulse-labelling experiments is described. The method involves the injection of model rhizodeposits, consisting of 14C-labelled glucose, root extract or root cell wall material, into the rooted soil of an unlabelled plant, simultaneously with the pulse-labelling of a separate but similar plant with 14CO2. In a growth chamber experiment with 30 day old wheat and barley the contribution of direct root respiration to 14C soil/root respiration over a 26 day period after labelling was estimated 89–95%. Estimates of direct root respiration in field-grown wheat and barley at different development stages in most cases accounted for at least 75% of 14C soil/root respiration over a 21 day period after labelling. The mineralization rate of injected 14C-glucose was positively correlated with the concentration of glucose-C established in soil. The use of the method in rhizosphere carbon budget estimations is evaluated.
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    Combined effect of salinity and hypoxia in wheat (Triticum aestivum L.) and wheat-Thinopyrum amphiploids (1994)
    Springer
    Plant and soil 166 (1994), S. 47-54 
    Details
    ISSN: 1573-5036
    Keywords: amphiploid ; hypoxia ; salinity ; Thinopyrum ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The effects of sodium chloride salinity and hypoxia were studied in eight wheat lines and three wheat-Thinopyrum amphiploids in vermiculite-gravel culture. The lines were treated with either 100 or 150 mol m−3 NaCl with and without hypoxia. Saline hypoxic conditions significantly reduced the vegetative growth, water use, grain and straw yields for all wheat varieties except the amphiploids, whereas NaCl or hypoxia alone had less pronounced effects. In addition, saline hypoxic stress reduced K+ concentration and increased significantly the Na+ and Cl− concentrations in cell sap expressed from leaves. There was more Na+ and Cl− accumulation in wheats than the amphiploids in hypoxic conditions at 150 mol m−3 NaCl. Of the wheats, Pato was the most sensitive at all stress levels while aTriticum aestivum cv. Chinese Spring ×Thinopyrum elongatum amphiploid was the most tolerant of the three amphiploids.
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    Effects of growth period, plant age and changes in solution aluminium concentrations on aluminium toxicity in wheat (1994)
    Springer
    Plant and soil 166 (1994), S. 21-30 
    Details
    ISSN: 1573-5036
    Keywords: aluminium ; growth period ; phosphorus ; plant age ; root length ; root width ; solution culture ; techniques ; Triticum aestivum ; variation ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The effects of growth period (time between transplanting and harvesting), plant age at which aluminium (Al) was added to solution, changes in Al concentration, and solution culture techniques (monitoring and adjusting solution Al concentrations thrice weekly or weekly replacement of the solutions) were investigated using a low ionic strength (2.7×10−3 M) solution culture technique. The wheat (Triticum aestivum L.) cultivars Waalt (Al-tolerant) and Warigal (Al-sensitive), or the near isogenic lines bred from these cultivars (RR for the Al-tolerant line and SS for the Al-sensitive line) were grown. In all experiments and treatments, Al additions were required to maintain the nominal concentration. The decline in solution Al concentrations was partially attributed to formation of an Al-hydroxy-phosphate precipitate with an Al:P molar ratio of 2.8 to 4.0. Increasing the growth period from 14 to 28 days increased Al sensitivity in Warigal but not in Waalt. When plants were exposed to Al for the same time, increasing the age of the plants that Al was added to solution decreased sensitivity to Al. Differential Al tolerance between the two lines was evident when solutions were monitored thrice weekly or replaced weekly. However, the Al concentration required to reduce relative yield by a given amount when the solutions were replaced weekly was about twice that when the solutions were monitored. With a constant growth period of 28 days, increasing solution Al concentrations for 3 or more days resulted in decreased yields at harvest. The exact effect depended on the cultivar, plant part (tops or roots), when solution Al concentrations were increased and the duration of the increase. For example, increasing Al concentrations from 5 μM to 20 μM for 10 days reduced yield in the RR line by approximately 50% in the tops and 30% in the roots beyond the effect of 5 M but had no effect in the SS line due to yields already being low at 5 μM. Adding 10 μM Al to solution for 6 days at the beginning of the experiment reduced yield by 25% in the RR line and 50% in the SS line. In contrast, adding 10 μM Al for 6 days in the middle of the growth cycle had no effect on the RR line but reduced yield by approximately 25% in the SS line. These results show that growth period, the age of the plants at which Al is added and the technique used (monitored or weekly replacement) all need to be considered when comparing results from different experiments. These results also show that the Al concentrations in solution need to be regularly monitored in long term experiments.
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    Redox transformations and plant uptake of selenium resulting from root-soil interactions (1994)
    Springer
    Plant and soil 158 (1994), S. 1-12 
    Details
    ISSN: 1573-5036
    Keywords: acid soils ; ascorbic acid ; barley ; gallic acid ; manganese oxides ; oxidation-reduction ; rhizosphere ; root exudates ; selenium ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Batch studies were conducted with Mn oxides (birnessite-hausmannite mixture, BHM) and samples of four soil series from the Mid-Atlantic region of the USA to determine effects of reducing organic acids, similar to those found in the rhizosphere, on the SeO3/SeO4 distribution. Jackland (Typic Hapludalf), Myersville (Ultic Hapludalf), Christiana (Aeric Paleaquult), and Evesboro (Typic Quartizipsamment) A and B horizon soil samples with and without prior Mn oxide reduction were incubated aerobically for 10 d with 0.1 mmol kg-1 SeO3 and 0 or 25 mmol kg-1 of ascorbic acid, gallic acid, oxalic acid, or citric acid. Selenite was also added to BHM (10 mmol kg-1) with 0 or 0.1 mmol kg-1 ascorbic acid. The availability of Se for plant uptake as a result of root-soil interactions was examined using growth chamber studies with barley (Hordeum vulgare L.) and wheat (Triticum aestivum L.) seedlings grown in 150-mL cone-shaped containers to maximize root-soil surface interactions and to create ‘rhizosphere’ soil throughout the root zone. In the BHM system ascorbic acid increased oxidation of SeO3 to SeO4 to 33% of added SeO3. In the presence of ascorbic and gallic acids and Mn oxides, oxidation of SeO3 to SeO4 occurred in the B horizons of all the soils and in the A horizons of Jackland and Myersville soils. Removal of Mn oxides decreased the oxidation in some samples. Wheat and barley plants were able to accumulate up to 20 μmol Se kg-1 from the Jackland soil when soluble Se was not measurable. The root-soil interactions in the Jackland soil with barley and wheat provided the plant with Se from insoluble sources. The results also indicate that Mn oxides coming in contact with reducing root exudates have a greater ability to oxidize SeO3 to SeO4. Thus, rhizosphere processes play an important role in the availability of Se for plant uptake.
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    URL: http://dx.doi.org/10.1007/BF00007911
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    Colonisation of wheat by VA-mycorrhizal fungi was found to be higher on a farm managed in an organic manner than on a conventional neighbour (1994)
    Springer
    Plant and soil 160 (1994), S. 33-40 
    Details
    ISSN: 1573-5036
    Keywords: organic agriculture ; phosphorus ; rock phosphate ; VA-mycorrhizas ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Levels of colonisation by vesicular-arbuscular (VA)-mycorrhizal fungi were compared between adjacent farms, one operated in a conventional manner and the other run according to organic farming principles. Wheat grown on the organic farm was found to have VA-mycorrhizal colonisation levels consistently 2 to 3 times higher than wheat on the conventional farm. Glasshouse and field trials indicated that the lower colonisation levels on the conventional farm were due to continual use of fertiliser containing soluble phosphorus (P). The fertiliser appeared to have an immediate negative effect on the rate of colonisation, and also appeared to have a long term negative effect through maintaining higher levels of soluble P in the soil, and by decreasing inoculum levels. Use of the relatively insoluble reactive rock phosphate fertiliser on the organic farm did not decrease levels of VA-mycorrhizas. Colonisation levels did not vary between wheat varieties, and herbicides and seed dressings were also not found to be having any significant effect on levels of colonisation.
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    URL: http://dx.doi.org/10.1007/BF00150343
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    Aluminum-induced deposition of (1,3)-β-glucans (callose) inTriticum aestivum L. (1994)
    Springer
    Plant and soil 162 (1994), S. 273-280 
    Details
    ISSN: 1573-5036
    Keywords: aluminum resistance ; (1, 3)-β-glucans ; callose ; roots ; stress indicator ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Aluminum (Al)-induced damage to leaves and roots of two Al-resistant (cv. Atlas 66, experimental line PT741) and two Al-sensitive (cv. Scout 66, cv. Katepwa) lines ofTriticum aestivum L. was estimated using the deposition of (1, 3)-β-glucans (callose) as a marker for injury. Two-day-old seedlings were grown for forty hours in nutrient solutions with or without added Al, and callose deposition was quantified by spectrofluorometry (0–1000 µM Al) and localized by fluorescence microscopy (0 and 400 µM Al). Results suggested that Al caused little damage to leaves. No callose was observed in leaves with up to 400 µM Al treatment. In contrast, root callose concentration increased with Al treatment, especially in the Al-sensitive lines. At 400 µM Al, root callose concentration of Al-sensitive Scout 66 was nearly four-fold that of Al-resistant Atlas 66. After Al treatment, large callose deposits were observed in the root cap, epidermis and outer cortex of root tips of Scout 66, but not Atlas 66. The identity of callose was confirmed by a reduced fluorescence in Al-treated roots: firstly, after adding an inhibitor of callose synthesis (2-deoxy-D-glucose) to the nutrient solution, and secondly, after incubating root sections with the callosedegrading enzyme β-D-glucoside glucohydrolase [EC 3.2.1.21]. Root callose deposition may be a good marker for Al-induced injury due to its early detection by spectrofluorometry and its close association with stress perception.
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    URL: http://dx.doi.org/10.1007/BF01347714
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    Gravitropic response growth angle and vertical distribution of roots of wheat (Triticum aestivum L.) (1994)
    Springer
    Plant and soil 165 (1994), S. 323-326 
    Details
    ISSN: 1573-5036
    Keywords: genotype ; gravitropic response ; root depth index (RDI)_ ; root growth angle ; root vertical distribution ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Recent work on root distribution, growth angles and gravitropic responses in Japanese cultivars of winter wheat are reviewed. Vertical distribution of roots, which influences the environmental stress tolerance of plants, was observed in the 12 Japanese cultivars in the field. The root depth index (RDI: the depth at which 50% of the root length has been reached) differed among the cultivars at the stem elongation stage. Since the RDI was closely related to the growth angle of seminal roots obtained in a pot experiment, it was assumed that growth angle is useful for predicting vertical root distribution among wheat genotypes. Gravitropic responses of the primary seminal root of 133 Japanese wheat cultivars assessed by measuring the growth angle in agar medium, were larger in the northern Japanese cultivars and smaller in the southern ones. It was also found that the geographical variation resulted from the wheat breeding process, i.e. genotypes with limited gravitropic responses of roots had been selected in the southern part of Japan where excessive soil moisture is one of the most serious problems.
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    URL: http://dx.doi.org/10.1007/BF00008076
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    Losses of14C from roots of pulse-labelled wheat and barley during washing from soil (1994)
    Springer
    Plant and soil 166 (1994), S. 93-99 
    Details
    ISSN: 1573-5036
    Keywords: barley ; 14C ; pulse-labelling ; roots ; washing losses ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract In crop carbon budget studies losses of root material during storage and washing of samples may cause considerable errors. To correct data from field experiments where rhizosphere C fluxes in wheat and barley were determined by14C pulse-labelling at different development stages, experiments were performed to quantify losses of14C from roots during washing. Losses of14C from wheat roots grown on nutrient solution and stored in different ways, decreased from on average 45% of total14C content 8 days after labelling to 27% after 21 days. This decrease was probably related to the incorporation of14C into structural compounds. During washing of oven-dried soil cores of held-grown wheat and barley 3 weeks after labelling, different size classes of losses of14C from the roots increased substantially with the development stage of the crop at labelling. The 0.3–0.6 mm size class increased from 5% of the14C in roots 〉 0.3 mm in young plants to 25% at ripening, and the 〈 0.3 mm size class increased from 8 to 41% of total14C content. The latter size class was, however, determined by washing handpicked roots and may therefore partly consist of adhering exudates, mucilages and microorganisms. The effect of development stage on root washing losses was attributed to root senescence which increases the fragility of roots. Thus, especially at the rate development stages root washing losses caused a severe underestimation of the root14C content. However, with these results the14C distribution patterns of the field experiments could be adequately corrected.
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    URL: http://dx.doi.org/10.1007/BF02185485
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    Differences in the metabolic responses of root tips of wheat and rye to aluminium stress (1994)
    Springer
    Plant and soil 167 (1994), S. 165-171 
    Details
    ISSN: 1573-5036
    Keywords: aluminium tolerance ; enzymes ; root tips ; rye ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The effects of aluminium (Al) ions on the metabolism of root apical meristems were examined in 4-day-old seedlings of two cereals which differed in their tolerance to Al: wheat cv. Grana (Al-sensitive) and rye cv. Dańkowskie Nowe (Al tolerant). During a 24 h incubation period in nutrient solutions containing 0.15 mM and 1.0 mM of Al for wheat and rye, respectively, the activity of first two enzymes in the pentose phosphate pathway (G-6-PDH and 6-PGDH) decreased in the sensitive cultivar. In the tolerant cultivar activities of these enzymes increased initially, then decreased slightly, and were at control levels after 24 h. In the Al-sensitive wheat cultivar a 50% reduction in the activity of 6-phosphogluconate dehydrogenase was observed in the presence of Al. Changes in enzyme activity were accompanied by changes in levels of G-6-P- the initial substrate in the pentose phosphate pathway. When wheat was exposed for 16 h to a nutrient solution containing aluminium, a 90% reduction in G-6-P concentration was observed. In the Al-tolerant rye cultivar, an increase and subsequently a slight decrease in G-6-P concentration was detected, and after 16 h of Al-stress the concentration of this substrate was still higher than in control plants. This dramatic Al-induced decrease in G-6-P concentration in the Al-sensitive wheat cultivar was associated with a decrease in both the concentration of glucose in the root tips as well as the activity of hexokinase, an enzyme which is responsible for phosphorylation of glucose to G-6-P. However, in the Al-tolerant rye cultivar, the activity of this enzyme remained at the level of control plants during Al-treatment, and the decrease in the concentration of glucose occurred at a much slower rate than in wheat. These results suggest that aluminium ions change cellular metabolism of both wheat and rye root tips. In the Al-sensitive wheat cultivar, irreversible disturbances induced by low doses of Al in the nutrient solution appear very quickly, whereas in the Al-tolerant rye cultivar, cellular metabolism, even under severe stress conditions, is maintained for a long time at a level which allows for root elongation to continue.
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    URL: http://dx.doi.org/10.1007/BF01587612
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    C-band polymorphism and structural rearrangements detected in common wheat (Triticum aestivum) (1994)
    Springer
    Euphytica 78 (1994), S. 1-5 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; C-band polymorphism ; structural rearrangements ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Giemsa C-banding allows for the identification of all 21 chromosome pairs of hexaploid wheat. However, variation in banding patterns of individual chromosomes and structural rearrangements exist between different cultivars making chromosome identification more difficult. The paper summarizes the available data on C-band polymorphism and structural rearrangement present in wheat cultivars and germplasms.
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    URL: http://dx.doi.org/10.1007/BF00021392
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    The effect of temperature on seed set and embryo development in reciprocal crosses of wheat and barley (1994)
    Springer
    Euphytica 78 (1994), S. 53-58 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; Hordeum vulgare ; barley ; intergeneric hybridization ; influence of temperature ; embryo development
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The effect of temperature on seed set and embryo development in reciprocal crosses of barley and wheat was assessed in crosses involving two spring barley varieties (Betzes, Martonvásári 50) and one wheat variety (Chinese Spring). Detached tillers placed in nutrient solution were pollinated in controlled environments at constant day-night temperature regimes (12, 15, 18 and 21° C) with a light intensity of 30,000 lux and a relative humidity of 80%. When barley was used as the female, lower temperatures (12 and 15° C) produced the maximum seed set, whereas for the reciprocal cross, the highest temperature (21° C) produced the best seed set in the Chinese Spring × Betzes combination. Low temperature retarded the embryo development. The highest numbers of hybrid plants were produced at 18° C and 21° C in the barley × wheat cross and in the wheat × barley cross, respectively. Embryos of about 1.5 mm length in the barley × wheat cross, and of about 1.0 mm length in the wheat × barley cross germinated successfully. The smallest embryo giving rise to hybrid plants was 0.57 mm in the barley × wheat cross and 0.51 mm in the wheat × barley cross.
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    URL: http://dx.doi.org/10.1007/BF00021397
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    Evaluation of Chinese Triticeae for resistance to Barley Yellow Dwarf Virus (BYDV) (1994)
    Springer
    Genetic resources and crop evolution 41 (1994), S. 35-41 
    Details
    ISSN: 1573-5109
    Keywords: wheat ; grass ; wide crossing ; China ; Barley Yellow Dwarf Virus (BYDV) ; luteovirus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Barley Yellow Dwarf Virus (BYDV) is recognised as a major pathological constraint to cereal production in northern China and several widespread epidemics have been reported. The host range of BYDV includes not only cereals but many grasses. The indigenous Triticeae of northern China have likely been exposed to significant disease pressure from BYDV and therefore may be a potential source of BYDV resistance for cereal improvement. A wide range of Triticeae accessions collected over three expeditions in northern China were evaluated for resistance to BYDV. Seedlings were artificially inoculated and virus levels then assayed by ELISA. Resistance and immunity to BYDV were found to be widely distributed among the seven genera of Triticeae included in the screening. A high proportion of resistant and immune accessions was found in the genera Hordeum, Leymus, Elymus and Elytrigia. The wide range of reaction types to BYDV found within many species, and even between accessions of some species, indicates that natural selection for BYDV resistance may have been relatively recent in the Chinese Triticeae. A high proportion of resistance and/or immunity was found in Xinjiang compared to the general distribution. From the Chinese Triticeae tested the Leymus species may be the most appropriate material to initiate transfer of BYDV resistance to wheat.
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    URL: http://dx.doi.org/10.1007/BF00051421
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    Mitochondrial DNA diseases: Histological and cellular studies (1994)
    Springer
    Journal of bioenergetics and biomembranes 26 (1994), S. 301-310 
    Details
    ISSN: 1573-6881
    Keywords: Mitochondrial encephalomyopathy ; mitochondrial DNA ; gene expression ; protein translation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Physics
    Notes: Abstract Large-scale deletions and tRNA point mutations in mitochondrial DNA (mtDNA) are associated with a variety of different mitochondrial encephalomyopathies. Skeletal muscle in these patients shows a typical pathology, characterized by the focal accumulation of large numbers of morphologically and biochemically abnormal mitochondria (ragged-red fibers). Both mtDNA deletions and tRNA point mutations impair mitochondrial translation and produce deficiencies in oxidative phosphorylation. However, mutant and wild-type mtDNAs co-exist (mtDNA heteroplasmy) and the translation defect is not expressed until the ratio of mutant: wild-type mtDNAs exceeds a specific threshold. Below the threshold the phenotype can be rescued by intramitochondrial genetic complementation. The mosaic expression of the skeletal muscle pathology is thus determined by both the cellular and organellar distribution of mtDNA mutants.
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    URL: http://dx.doi.org/10.1007/BF00763101
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    Ethylene as promoter of wheat grain maturation and ear senescence (1994)
    Springer
    Plant growth regulation 15 (1994), S. 107-112 
    Details
    ISSN: 1573-5087
    Keywords: aminoethoxyvinylglycine ; ear senescence ; ethephon ; ethylene ; grain maturation ; silver thiosulfate ; Triticum aestivum ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract This work was aimed at testing the involvement of ethylene in the maturation of grain and senescence of the foliar structures of the wheat inflorescence. Whole wheat ears emitted ethylene to the atmosphere. From pre-anthesis, ethylene emission progressively increased from 0.76 nl g−1FW h−1 to a peak 1.53 nl g−1FW h−1 at the hard dough stage of the grains, to fall to a minimum of 0.10 nl g−1FW h−1 at the dormant seed stage. Ethephon increased the ethylene release, hastened the process of grain maturation and senescence of the ears. Aminoethoxyvinylglycine and silver thiosulfate produced the opposite effects. It is concluded that ethylene plays a role in grain maturation and in the senescence of the green bracts of the inflorescence.
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    URL: http://dx.doi.org/10.1007/BF00024098
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    Gibberellins and α-amylase gene expression in germinating wheat grains (1994)
    Springer
    Plant growth regulation 15 (1994), S. 261-270 
    Details
    ISSN: 1573-5087
    Keywords: abscisic acid ; α-amylase ; germination ; gibberellin(s) ; paclobutrazol ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Gibberellins (GAs), GA8, GA17, GA19, GA20, GA29, and GA79 were identified by full-scan gas chromatography-mass spectrometry in a purified acidic fraction and GA8, GA20, GA79, and GA90 in a hydrolysed conjugate fraction from mature wheat grains. Gibberellin A20-13-O-glucoside was also quantified directly as the permethyl derivative in dry seed. The scutellum was identified as the major site of de novo GA biosynthesis by measuring ent-kaurene accumulation in vivo in grains treated with 2S,3S-paclobutrazol. Several GAs of the early 13-hydroxylation GA pathway began to accumulate in the axis and scutellum between 24 and 48 hours in untreated grains germinated at 15°C. Bioactive GA1 and GA3 also increased in the endosperm during this period, whereas abscisic acid contents of embryo and endosperm declined rapidly over 48 hours following imbibition. Treating grains with 2S,3S-paclobutrazol reduced GA1 plus GA3 content of scutella by 70–80% over 4 days without affecting significantly the steady-state pool of α-amylase mRNA transcripts. In contrast, a 50–80% reduction in the content of bioactive GAs in the endosperm was associated with a 70–78% decrease in transcripts for both α-amylase gene families in aleurones of paclobutrazol-treated grains. It was concluded that the initiation of α-amylase gene expression in wheat scutella was independent of de novo GA biosynthesis, whereas that in the aleurone was largely dependent on embryo-produced GAs.
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    URL: http://dx.doi.org/10.1007/BF00029899
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    Effectiveness of different phosphatic fertilizers measured using labelled superphosphate and phosphorus taken up by plants (1994)
    Springer
    Nutrient cycling in agroecosystems 39 (1994), S. 31-37 
    Details
    ISSN: 1573-0867
    Keywords: Compost ; diammonium phosphate ; phosphorus availability ; fertilizer effectiveness ; 32P ; rock phosphate ; superphosphate ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The agronomic effectiveness of three P fertilizers (diamonium phosphate, rock phosphate and compost) was studied in a greenhouse experiment using wheat. A radioisotopic method, using triple superphosphate labelled with32P, was used to evaluate the P in dried tops that was derived from i) the soil, ii) labelled superphosphate and iii) the fertilizer being studied. The ratio between P uptake from each fertilizer and P uptake from the soil was used to compare the effectiveness of the different fertilizers. P derived from diammonium phosphate was greater than P derived from the soil, except in one soil. P derived from rock phosphate was always lower than P derived from the soil. The effectiveness of compost depended on soil type. Compost can produce two kind of effects: i) a direct P contribution and ii) an indirect effect improving P uptake from the soil. The radioisotopic method can be used to study the effectiveness of fertilizers even when there are no differences in yield.
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    Large granules, nests or bands: Methods of increasing efficiency of fall-applied urea for small cereal grains in North America (1994)
    Springer
    Nutrient cycling in agroecosystems 38 (1994), S. 61-87 
    Details
    ISSN: 1573-0867
    Keywords: Band placement ; barley ; cereal grains ; fall-applied N ; fertilizer efficiency ; large urea granules ; LUG ; method of placement ; nest placement ; nitrification ; time of application ; urea fertilizer ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract In North America where the climate is cool enough only one crop is grown yearly, N fertilizers are sometimes applied in the previous fall rather than in the spring for fall- or spring-sown cereal grains. However, in areas where snow accumulates in winter, fall application of N fertilizers is generally inferior to spring application. Substantial nitrification takes place in winter and subsequent N loss occurs primarily in early spring by denitrification after the snow melt. Immobilization of N is also greater with fall- than spring-applied N fertilizers. Nitrogen is more efficiently retained in the soil as NH4 and thus more effectively used by plants if formation of nitrite (NO2) and NO3 is reduced or prevented by inhibiting nitrification. The nitrification is reduced when urea is placed in bands, because of high pH, ammonia concentration and osmotic pressure in the soil. The rate of nitrification is further reduced when urea is placed in widely-spaced nests (a number of urea prills placed together at a point below the soil surface) or as large urea granules (LUG) by reducing contact between the nitrifying bacteria and the NH4 released upon urea hydrolysis. A further reduction in nitrification from LUG can be obtained by addition of chemical nitrification inhibitors (such as dicyandiamide (DCD)) to LUG. The concentration of a chemical inhibitor required to suppress nitrification decreases with increasing granule size. The small soil-fertilizer interaction zone with placement of urea in nests or as LUG also reduces immobilization of fertilizer N, especially in soils amended with crop residues. The efficiency of fall-applied N is improved greatly by placing urea in nests or as LUG for small cereal grains. Yields of spring-sown barley from nests of urea or LUG applied in the fall are close to those obtained with spring-applied urea prills incorporated into the soil. Delaying urea application until close to freeze-up is also improved the efficiency of fall-applied N. This increased effectiveness of urea nests or LUG is due to slower nitrification, lower N loss over the winter by denitrification, and reduced immobilization of applied N. Fall application of LUG containing low rates of DCD slows nitrification, reduces over-winter N loss, and causes further improvement in yield and N uptake of winter wheat compared to urea as LUG alone in experiments in Ontario; in other experiments in Alberta there is no yield advantage from using a nitrification inhibitor with LUG for barley. Placement of LUG or nests of urea in soil is an agronomically sound practice for reducing N losses. This practice can eliminate or reduce the amount of nitrification inhibitor necessary to improve the efficiency of fall-applied urea where losses of mineral N are a problem. The optimum size of urea nest or LUG, and optimum combination of LUG and an efficient nitrification inhibitor need to be determined for different crops under different agroclimatic conditions. The soil (texture, CEC, N status), plant (winter or spring crop, crop geometry, crop growth duration and cultivar) and climatic (temperature, amount and distribution of precipitation) factors should be taken into account during field evaluation of LUG. There is a need to conduct region-specific basic research to understand mechanisms and magnitudes of N transformations and N losses in a given ecosystem. Prediction of nitrification from LUG or urea nests in various environments is needed. In nitrification inhibition studies with LUG and chemical nitrification inhibitors, measurements of nitrifier activity will be useful. Finally, there is need for development of applicators for mechanical placement of LUG or urea prills in widely-spaced nests in soil.
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    Effect of selenium-enriched calcium nitrate, top-dressed at different growth stages, on the selenium concentration in wheat (1994)
    Springer
    Nutrient cycling in agroecosystems 38 (1994), S. 199-203 
    Details
    ISSN: 1573-0867
    Keywords: calcium nitrate ; growth stages ; sodium selenate-enriched fertilizers ; Se concentration ; silty clay soil ; top-dressing ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A greenhouse experiment was conducted to evaluate the effect of Se contained in calcium nitrate, top-dressed at different growth stages, on the Se concentration in wheat (Triticum aestivum L.). Selenium as sodium selenate was added to Ca (NO3)2 and NPK (21-4-10) during the manufacturing process. A silty clay soil with soil pH of 6.1 was used. Four selenium treatments incorporated in Ca (NO3)2 were top-dressed at both the tillering and heading growth stages at rates of 0, 15, 30, and 45 mg kg−1 of Ca (NO3)2 fertilizer equivalent to about 0, 0.003, 0.007, 0.01 mg Se kg−1 soil, respectively. A fifth treatment of 20 mg Se kg−1 of NPK (21-4-10%) equivalent to 0.007 mg Se kg−1 soil was basal dressed at the time of sowing. Calcium nitrate with or without Se was top-dressed at the rate of 35 mg N kg−1. In addition all pots received a basal dose of N at the rate of 7 0 mg N kg−1 through a NPK(21-4-10) fertilizer. The Se-enriched Ca (NO3)2 increased the uptake and concentration of Se in wheat significantly (ρ〉0.05) with increasing concentration of Se in the fertilizer applied. The Se concentration in wheat grain increased from 〈1.1 to 468µg Se kg−1 in the first year when the concentration in the Se-enriched Ca (NO3)2 was increased from 0 to 45 mg Se kg−1 but the corresponding increase in the second and third year was lower. The Se concentration in the grain was more than twice of that in the straw. The uptake and concentration of Se in wheat, except in the second year, was generally higher when Se was top-dressed at heading as compared to that when it was top-dressed at tillering but the concentration differences between time of application were not statistically significant(ρ〉0.05). Basal application of Se-enriched NPK (0.007 mg Se kg−1 soil) was only half as effective as an equivalent rate of Se in top-dressed Seenriched Ca(NO3)2 in increasing the Se concentration in wheat and the concentration levels among these treatments were significantly (ρ〉0.01) different. It was concluded that topdressing of Se-enriched Ca(NO3)2 at 30 mg Se kg−1 is an effective method of application to increase the Se concentration in wheat grain to a level, 〉 100µg kg−1 dry matter, considered adequate for human consumption.
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    URL: http://dx.doi.org/10.1007/BF00749692
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    Photosynthetic electron transport and anaerobic metabolism in purple non-sulfur phototrophic bacteria (1994)
    Springer
    Antonie van Leeuwenhoek 66 (1994), S. 151-164 
    Details
    ISSN: 1572-9699
    Keywords: purple non-sulfur bacteria ; Rhodobacter ; photosynthesis ; CO2 fixation ; anaerobic respiration ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Purple non-sulfur phototrophic bacteria, exemplifed byRhodobacter capsulatus andRhodobacter sphaeroides, exhibit a remarkable versatility in their anaerobic metabolism. In these bacteria the photosynthetic apparatus, enzymes involved in CO2 fixation and pathways of anaerobic respiration are all induced upon a reduction in oxygen tension. Recently, there have been significant advances in the understanding of molecular properties of the photosynthetic apparatus and the control of the expression of genes involved in photosynthesis and CO2 fixation. In addition, anaerobic respiratory pathways have been characterised and their interaction with photosynthetic electron transport has been described. This review will survey these advances and will discuss the ways in which photosynthetic electron transport and oxidation-reduction processes are integrated during photoautotrophic and photoheterotrophic growth.
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    URL: http://dx.doi.org/10.1007/BF00871637
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  • 87
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    Effect of increasing distance fromAcacia nilotica trees on wheat yield (1994)
    Springer
    Agroforestry systems 25 (1994), S. 23-29 
    Details
    ISSN: 1572-9680
    Keywords: Acacia nilotica ; wheat ; border trees ; crop yield ; Pakistan
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Planting trees in the cultivated fields of Pakistan is a controversial topic between foresters and agriculturists. Some farmers believe that trees significantly reduce their crop yields; therefore they avoid planting trees in their fields. On the other hand, many foresters claim trees are beneficial for crops. This study was conducted to determine the influence of boundary trees (Acacia nilotica) on the growth and yield of associated wheat crops under irrigated conditions in Punjab, Pakistan. Results indicate that close proximity to trees adversely affected tillers/m2, weight/1000 grain and the grain yield of wheat planted up to a distance of 8.5 m from the trees. Plant height and grains/spike were least affected. In general, the growth and yield of wheat improved as distance from the tree increased. Tree size did not affect wheat height, tillers/m2, grains/spike or weight/1000 grain. The grain yields were slightly lower near the largest trees (50–54.9 cm DBH trees).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00705704
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  • 88
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    Strategies for improving heterologous protein production from filamentous fungi (1994)
    Springer
    Antonie van Leeuwenhoek 65 (1994), S. 245-250 
    Details
    ISSN: 1572-9699
    Keywords: Aspergillus ; gene expression ; heterologous protein ; protein secretion ; Trichoderma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Despite the naturally high capacity for protein secretion by many species of filamentous fungi, secteted yields of many heterologous proteins have been comparatively low. The strategies for yield improvement have included the use of strong homologous promoters, increased gene copy number, gene fusions with a gene encoding a naturally well-secreted protein, protease-deficient host strains and screening for high yields following random mutagenesis. Such approaches have been effective with some target heterologous proteins but not others. Approaches used in heterologous protein production from filamentous fungi are discussed and a perspective on emerging strategies is presented.
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    URL: http://dx.doi.org/10.1007/BF00871952
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  • 89
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    Photobiology of Bacteria (1994)
    Springer
    Antonie van Leeuwenhoek 65 (1994), S. 331-347 
    Details
    ISSN: 1572-9699
    Keywords: photoactive proteins ; photoreceptors ; chromophores ; energy transduction ; light signalling ; phototaxis ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The field of photobiology is concerned with the interactions between light and living matter. For Bacteria this interaction serves three recognisable physiological functions: provision of energy, protection against excess radiation and signalling (for motility and gene expression). The chemical structure of the primary light-absorbing components in biology (the chromophores of photoactive proteins) is surprisingly simple: tetrapyrroles, polyenes and derivatised aromats are the most abundant ones. The same is true for the photochemistry that is catalysed by these chromophores: this is limited to light-induced exciton- or electron-transfer and photoisomerization. The apoproteins surrounding the chromophores provide them with the required specificity to function in various aspects of photosynthesis, photorepair, photoprotection and photosignalling. Particularly in photosynthesis several of these processes have been resolved in great detail, for others at best only a physiological description can be given. In this contribution we discuss selected examples from various parts of the field of photobiology of Bacteria. Most examples have been taken from the purple bacteria and the cyanobacteria, with special emphasis on recently characterised signalling photoreceptors inEctothiorhodospira halophila and inFremyella diplosiphon.
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    URL: http://dx.doi.org/10.1007/BF00872217
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  • 90
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    Powdery mildew resistance in Aegilops tauschii coss. and synthetic hexaploid wheats (1994)
    Springer
    Genetic resources and crop evolution 41 (1994), S. 151-158 
    Details
    ISSN: 1573-5109
    Keywords: Triticum aestivum ; Aegilops tauschii (syn. Ae. squarrosa) ; Erysiphe graminis f. sp. tritici resistance genes ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary A collection of 400 Ae. tauschii (syn. Ae. squarrosa) Coss. accessions were screened for powdery mildew resistance based on the response patterns of 13 wheat cultivars/lines possessing major resistance genes to nine differential mildew isolates. 106 accessions showed complete resistance to all isolates, and 174 accessions revealed isolate-specific resistance, among which were 40 accessions exhibiting an identical response pattern as wheat cultivar ‘Ulka/*8Cc’ which is known to possess resistance gene Pm2. Expression of both complete and isolate-specific resistance from Ae. tauschii was observed in some synthetic hexaploid wheats derived from four mildew susceptible T. durum Desf. parents, each crossed with five to 38 resistant diploid Ae. tauschii accessions. Synthetic amphiploids involving different combinations of T. durum and Ae. tauschii generally showed a decrease in resistance compared with that expressed by the Ae. tauschii parental lines.
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    URL: http://dx.doi.org/10.1007/BF00051631
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  • 91
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    Effect of induction medium pH and maltose concentration on in vitro androgenesis of hexaploid winter triticale and wheat (1994)
    Springer
    Plant cell, tissue and organ culture 39 (1994), S. 49-53 
    Details
    ISSN: 1573-5044
    Keywords: agar ; anther culture ; Ficoll ; maltose ; pH ; triticale ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Low levels of in vitro androgenesis limit the utility of anther culture as a routine tool for the improvement of triticale. The objectives of this research were to determine the effect of induction medium modifications on the embryoid induction (EI) and green plant regeneration (GPR) of three hexaploid winter triticales and a hexaploid winter wheat. Medium modifications were factorial combinations of gelling agents, pH and maltose concentration. There was a significant difference in the response of wheat and triticales. An induction medium pH of 4.8 vs. 5.8 led to higher EI percentages in all cases and in Ficoll containing medium to a significantly higher GPR in the wheat, but it had no effect on the response of the triticales. Maltose at 0.26 M vs. 0.21 M increased the EI of both the triticales and the wheat but led to higher GPR only in the case of wheat. Averaged over genotypes, induction media with agar and Ficoll 400 were superior to the liquid form. In terms of GPR the wheat gave the highest response: 9.1%. The GPR percentages for the triticales ranged from 1.4 to 7.1. Genotype specificity must be overcome if anther culture is to be routinely used in diverse arrays of triticale germplasm.
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    URL: http://dx.doi.org/10.1007/BF00037591
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  • 92
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    Heterosis of grain weight in wheat hybrids with Triticum timopheevi cytoplasm (1994)
    Springer
    Euphytica 75 (1994), S. 189-193 
    Details
    ISSN: 1573-5060
    Keywords: Grain filling characteristics ; heterosis ; Triticum timopheevi cytoplasm ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Two kinds of wheat hybrids with the same nuclear genotype but different cytoplasms (one with T.timopheevi cytoplasm, i.e., A/R, and the other with T.aestivum cytoplasm, i.e., B/R) were produced by two 3 × 5 incomplete diallel crosses of 3 A-lines, 3 corresponding B-lines and 5 R-lines, respectively. Experimental results did not show significant differences between the hybrids of A/R and B/R in grain filling characteristics and grain weight. The beterosis of grain weight seems mainly determined by the nuclear genotype. Although the seeds set on most A-lines were shrivelled, such a phenomenon was not found in grains set on F1. The duration of the lag period (D1) and the average grain filling rates during the linear period and the mature period (i.e., FR2 and FR3) were significantly and positively related to 1000-grain weight. It was in these factors that most hybrids displayed clear mid-parent (MP) heterosis. The amount of grain weight heterosis was not significantly related to MP value. This indicates that the grain weight heterosis of wheat hybrids will not decrease with an increase of the MP value.
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    URL: http://dx.doi.org/10.1007/BF00025603
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  • 93
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    Genetics of leaf rust resistance in 13 accessions of the Watkins wheat collection (1994)
    Springer
    Euphytica 80 (1994), S. 151-155 
    Details
    ISSN: 1573-5060
    Keywords: leaf rust resistance ; Puccinia recondita ; Triticum aestivum ; wheat ; genetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The inheritance of leaf rust resistance was studied in 13 accessions of the A.E. Watkins wheat collection. Eight of the accessions (V409, V624, V628, V712, V731, V734, V745, and V855) were shown to have gene Lr33 and four of these (V409, V624, V628, and V731) also have LrW. Accessions V624 and V338 have LrB, and V377 and V488 have Lr11. V46 has an unidentified gene that gives an intermediate level of resistance. V860 has a partially dominant gene that gives a fleck reaction to avirulent isolates in the seedling stage. This gene is different from LrW and may be previously unidentified. It has been assigned the temporary gene symbol LrW2. In addition to seedling-effective genes, V46, V731, and V745 may have Lr34 and V745 may have Lr13. The adult-plant resistance in V488, V624, and V860 could not be identified. Seedling gene LrW2 and some of the adult-plant resistance should be useful sources of resistance.
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    URL: http://dx.doi.org/10.1007/BF00039311
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  • 94
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    Evolution of virulence patterns in yellow rust races and its implications for Ereeding for resistance in wheat in Kenya (1994)
    Springer
    Euphytica 80 (1994), S. 165-170 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; Puccinia striiformis ; yellow rust ; durable resistance ; race-specific resistance ; residual resistance ; races ; virulence, Kenya
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Virulence patterns of yellow rust isolates collected in Kenya between 1986–1989 were compared with earlier results. The number of virulence factors per race and the range in virulence factors both increased considerably. Before 1976 races carried on average 4.5 to 5.0 virulence factors, whereas the races after 1986 had a mean of 6.5 virulence factors. The range in the number of virulence factors increased from some seven to eight in the first period to 12 in the second out of the 17 evaluated. In the period 1986–1989 another three virulence factors (2, 9 and A) were assessed. All three occurred at a high frequency. Virulence neutralizing the resistance genes Yr2, Yr2+, Yr6, Yr6+, Yr7, Yr7+, Yr8, Yr9, Yr9+ and those in the cultivars Anza (A), Strubes Dickkopf (SD) and Suwon92/Omar (SU) occurred at a high frequency, while virulence for Yr3V, Yr4+, Yr5, CV and SP (resistance in Carstens V and Spaldings Prolific resp.) were not found. The remaining three virulence factors for Yr1, 10 and 3N were rare. In the past ten years the resistance of most released cultivars became ineffective in less than six years. They were shown to carry race-specific major resistance genes such as Yr7+, Yr9+, SD and A. However, in the field, the resistance of the cultivars was not completely neutralized. A residual resistance, ranging from moderate to fairly high, was observed in all cultivars in which the major gene resistances were neutralized by corresponding virulence genes. Other wheat cultivars such as Africa Mayo, Kenya Kudu, Enkoy, Kenya Leopard, Bounty, Frontatch, Bonny and Kenya Plume appeared to keep their resistance over a condiserable period of time. They are considered to be durably resistant to the Kenyan yellow rust populations. This form of resistance, together with the residual resistance, can be recommended for use in breeding programmes.
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    URL: http://dx.doi.org/10.1007/BF00039647
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    Molecular biology of C4 phosphoenolpyruvate carboxylase: Structure, regulation and genetic engineering (1994)
    Springer
    Photosynthesis research 39 (1994), S. 115-135 
    Details
    ISSN: 1573-5079
    Keywords: C4 photosynthesis ; gene expression ; oligomerization ; phosphorylation-dephosphorylation cascade ; PEPC-protein kinase ; site-directed mutagenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Three to four families of nuclear genes encode different isoforms of phosphoenolpyruvate (PEP) carboxylase (PEPC): C4-specific, C3 or etiolated, CAM and root forms. C4 leaf PEPC is encoded by a single gene (ppc) in sorghum and maize, but multiple genes in the C4-dicot Flaveria trinervia. Selective expression of ppc in only C4-mesophyll cells is proposed to be due to nuclear factors, DNA methylation and a distinct gene promoter. Deduced amino acid sequences of C4-PEPC pinpoint the phosphorylatable serine near the N-terminus, C4-specific valine and serine residues near the C-terminus, conserved cysteine, lysine and histidine residues and PEP binding/catalytic sites. During the PEPC reaction, PEP and bicarbonate are first converted into carboxyphosphate and the enolate of pyruvate. Carboxyphosphate decomposes within the active site into Pi and CO2, the latter combining with the enolate to form oxalacetate. Besides carboxylation, PEPC catalyzes a HCO3 --dependent hydrolysis of PEP to yield pyruvate and Pi. Post-translational regulation of PEPC occurs by a phosphorylation/dephosphorylation cascade in vivo and by reversible enzyme oligomerization in vitro. The interrelation between phosphorylation and oligomerization of the enzyme is not clear. PEPC-protein kinase (PEPC-PK), the enzyme responsible for phosphorylation of PEPC, has been studied extensively while only limited information is available on the protein phosphatase 2A capable of dephosphorylating PEPC. The C4 ppc was cloned and expressed in Escherichia coli as well as tobacco. The transformed E. coli produced a functional/phosphorylatable C4 PEPC and the transgenic tobacco plants expressed both C3 and C4 isoforms. Site-directed mutagenesis of ppc indicates the importance of His138, His579 and Arg587 in catalysis and/or substrate-binding by the E. coli enzyme, Ser8 in the regulation of sorghum PEPC. Important areas for further research on C4 PEPC are: mechanism of transduction of light signal during photoactivation of PEPC-PK and PEPC in leaves, extensive use of site-directed mutagenesis to precisely identify other key amino acid residues, changes in quarternary structure of PEPC in vivo, a high-resolution crystal structure, and hormonal regulation of PEPC expression.
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    URL: http://dx.doi.org/10.1007/BF00029380
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    Scaling CO2-photosynthesis relationships from the leaf to the canopy (1994)
    Springer
    Photosynthesis research 39 (1994), S. 321-350 
    Details
    ISSN: 1573-5079
    Keywords: big leaf ; conductance ; forest ; model ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Responses of individual leaves to short-term changes in CO2 partial pressure have been relatively well studied. Whole-plant and plant community responses to elevated CO2 are less well understood and scaling up from leaves to canopies will be complicated if feedbacks at the small scale differ from feedbacks at the large scale. Mathematical models of leaf, canopy, and ecosystem processes are important tools in the study of effects on plants and ecosystems of global environmental change, and in particular increasing atmospheric CO2, and might be used to scale from leaves to canopies. Models are also important in assessing effects of the biosphere on the atmosphere. Presently, multilayer and big leaf models of canopy photosynthesis and energy exchange exist. Big leaf models — which are advocated here as being applicable to the evaluation of impacts of ‘global change’ on the biosphere — simplify much of the underlying leaf-level physics, physiology, and biochemistry, yet can retain the important features of plant-environment interactions with respect to leaf CO2 exchange processes and are able to make useful, quantitative predictions of canopy and community responses to environmental change. The basis of some big leaf models of photosynthesis, including a new model described herein, is that photosynthetic capacity and activity are scaled vertically within a canopy (by plants themselves) to match approximately the vertical profile of PPFD. The new big leaf model combines physically based models of leaf and canopy level transport processes with a biochemically based model of CO2 assimilation. Predictions made by the model are consistent with canopy CO2 exchange measurements, although a need exists for further testing of this and other canopy physiology models with independent measurements of canopy mass and energy exchange at the time scale of 1 h or less.
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    URL: http://dx.doi.org/10.1007/BF00014590
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    Carbon translocation to the rhizosphere of maize and wheat and influence on the turnover of native soil organic matter at different soil nitrogen levels (1994)
    Springer
    Plant and soil 161 (1994), S. 233-240 
    Details
    ISSN: 1573-5036
    Keywords: C distribution ; native soil organic matter ; rhizosphere ; root released carbon ; wheat ; Zea mays
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Wheat and maize were grown in a growth chamber with the atmospheric CO2 continuously labelled with 14C to study the translocation of assimilated carbon to the rhizosphere. Two different N levels in soil were applied. In maize 26–34% of the net assimilated 14C was translocated below ground, while in wheat higher values (40–58%) were found. However, due to the much higher shoot production in maize the total amount of carbon translocated below ground was similar to that of wheat. At high N relatively more of the C that was translocated to the root, was released into the soil due to increased root respiration and/or root exudation and subsequent microbial utilization and respiration. The evolution rate of unlabelled CO2 from the native soil organic matter decreased after about 25 days when wheat was grown at high N as compared to low N. This negative effect of high N in soil was not observed with maize.
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    URL: http://dx.doi.org/10.1007/BF00046394
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    Root length and biomass losses during sample preparation with different screen mesh sizes (1994)
    Springer
    Plant and soil 161 (1994), S. 299-303 
    Details
    ISSN: 1573-5036
    Keywords: faba bean ; root length density ; root measurement methods ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Data are presented on the differences in root length density (RLD), dry matter (DM), and root diameter values determined on wheat and faba bean using sieves of different mesh size to separate roots from soil during sample preparation. Screens with 0.2, 1, and 2 mm (0.04, 1, and 4 mm2) aperture were used. Roots collected on the 2-mm sieve represented on average 55% of the weight and only 10% of the total length collected using a 0.2-mm sieve. With a 1-mm sieve 75% of weight was retained, but only 34% of the length. In the 0–20 cm soil layer average RLD and DM values ranged between 1.3 and 2.5 cm cm-3 and 215 and 136 g m-2 for faba bean and wheat respectively with 2 mm screens and 14.6 and 18.1 cm cm-3 and 313 and 202 g m-2 with 0.2 mm sieves. RLD was more affected than weight since losses from coarse screens were largely due to fine root fractions, although the 1-and 2-mm screens retained a small amount of fine roots that were long or attached to main structures. Variability was higher for measurements on coarser screens. The use of screens much coarser than the diameter of fine roots is not recommended for the study of surface-related phenomena in which root length quantification is necessary, while it may be acceptable for gross comparisons of root weight and spatial extent.
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    URL: http://dx.doi.org/10.1007/BF00046401
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  • 99
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    Combining abilities of in vitro traits in wheat (Triticum aestivum L.) immature embryo cultures (1994)
    Springer
    Euphytica 76 (1994), S. 169-175 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; combining ability ; in vitro culture ; genotypic and phenotypic correlations ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Combining ability for six in vitro culture traits in wheat were studied in a 8×8 diallel cross (excluding reciprocals). Specific combining ability effects (sca) were significant for all six traits derived from immature embryos on two media protocols, whereas general combining ability (gca) variances were significant only for five of them. Furthermore, based on ratios obtained by comparing the ratio of K2 gca to K2 sca, sca was more important than gca for all six traits. Genetic correlations between shoot formation and other in vitro traits, except callus weight and root formation, were higher in magnitude than the corresponding phenotypic correlations estimates, indicating the importance of genetic effects.
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    URL: http://dx.doi.org/10.1007/BF00022161
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  • 100
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    Gene action and heritability for photosynthetic activity in two wheat crosses (1994)
    Springer
    Euphytica 76 (1994), S. 235-238 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; photosynthesis ; gene action ; heritability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Gene action and heritability for photosynthetic activity were estimated from generation means in two wheat crosses during two stages (5 th leaf and flag leaf between 2 and 5 days after anthesis). Six generations were available for each cross: parents (P1 and P2), F1, F2 and backcrosses (BC1 and BC2). Correlations between some morphophysiological characters and photosynthetic activity of the flag leaf was also determined. The joint scaling test described by Mather & Jinks was used to determine the gene action. It showed that them; [d]; [h]; [i], [l] (mean, additivity, dominance, additive x additive interallelic interaction effects, dominance x dominance interallelic interaction effects) model fits the two crosses at both measurement times. All the model genetic components were significant for the flag leaf, however for the 5 th leaf only [h]; [i] and [l] were significant. The presence of additive and additive x additive effects suggested the possibility of selecting for this character using the flag leaf so as to obtain pure inbred lines. Dominance effects [h] were negative and dominance x dominance effects [l] were positive. Broad sense heritability values were medium to low. There were no correlations between the studied morphophysiological characters and the photosynthetic activity.
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    URL: http://dx.doi.org/10.1007/BF00022168
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