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  • Genetics  (72)
  • Wiley-Blackwell  (72)
  • American Chemical Society
  • American Geophysical Union
  • American Meteorological Society
  • Elsevier
  • 1980-1984  (72)
  • 1925-1929
  • 1983  (38)
  • 1982  (34)
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  • 1980-1984  (72)
  • 1925-1929
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  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 1-6 
    ISSN: 0192-253X
    Keywords: glycerol-3-phosphate dehydrogenase ; isozymes ; mice ; genetics ; development ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Genetic variants that affect the heat stability and ionic charge of the adult isozyme of glycerol-3-phosphate dehydrogenase (EC 1.1.1.8) map to a gene, Gdc-1, located on chromosome 15. A second isozyme of glycerol-3-phosphate dehydrogenase, structurally homologous to the product of the Gdc-1 locus and expressed predominantly in undifferentiated tissues, has previously been identified. We have now discovered an electrophoretic variant of this embryonic isozyme. This expression is determined by a codominant allele of the gene, Gdc-2, that maps to the distal end of chromosome 9 as inferred from the observed gene order Mpi-1-d-Mod-1-Gdc-2.
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  • 2
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 273-273 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 3
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 299-308 
    ISSN: 0192-253X
    Keywords: survival ; selection ; heat-shock proteins ; Drosophila melanogaster ; temperature compensation ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Two stocks of Drosophila melanogaster, one sensitive (6.5% survival) and one resistant (76.24%) to heat shock (40°C/25 min) were derived through indirect selection [1]. Genetic analysis of heat-sensitive and heat-resistant lines we had selected revealed that the survival rate is chiefly determined by cytoplasmic inheritance but also depends to some extent on the nucleus [1]. The ability of the fly to survive thermal stress was found to have an excellent correlation with the kinetics of protein synthesis in ovaries or glands subjected to heat treatment. The incorporation rate of 35S-methionine into proteins was found to be higher for strains exhibiting higher survival (R1, R1S1) than for strains with a lesser ability (S1, S1 R1) to survive heat shock. Moreover, the intensity of labeling of the proteins synthesized and especially of the hsps (heat-shock proteins) after the heat shock is higher in the R1 and R1S1 stocks than in the S1 and S1R1 stocks. This convergence between survival and the cellular level of hsps (both manipulated by selection) bears on the physiological significance of these proteins which seems to participate in the control of the survival as an additive component.
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  • 4
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 371-372 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 5
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983), S. 21-29 
    ISSN: 0192-253X
    Keywords: agouti locus ; embryonic lethal ; ax ; lethal nonagouti ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The time and mode of action of the homozygous ax gene, lethal nonagouti, has been investigated on the inbred AX/Pa background. Heterozygotes were mated inter se to produce 25% homozygous embryos and heterozygotes were mated with homozygous, nonagouti mice to provide control litters. Comparisons of the frequency of mating success, the ratio of implantation sites to ovarian ovulation sites, and the average litter sizes between experimental and control matings all indicated that ax/ax embryos are not lost prior to implantation. Histological examination of pregnant uteri indicated that ax/ax embryos are first evident as abnormal blastocysts at 4.5 days post coitum (pc). These implant and develop to varying degrees, some differentiating trophoblast giant cells and a primitive endoderm layer. Growth is retarded and only small, disorganized clumps of tissue remain by 7.5 and 8.5 days pc. The time and mode of gene action of lethal nonagouti is thus different from its allele, lethal Yellow.
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  • 6
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983), S. 61-68 
    ISSN: 0192-253X
    Keywords: cell adhesion ; macromolecular ; sponge factors ; Dictyostelium ; adhesion-blocking antiserum ; staggerer mutant ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Cellular adhesion is what keeps cells together in multicellular organisms. Cells adhere to each other, to extracellular matrices, and to the substratum. Biochemical analyses of these processes have suggested some of the types of surface molecules which may be involved, but definitive evidence must rely on effective reconstruction of functional membranes or genetic alteration of the pertinent genes. Together these approaches may give us a better understanding of how cells sort out and form tissues during development.
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  • 7
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 197-205 
    ISSN: 0192-253X
    Keywords: mouse fetal erythrocyte antigen ; erythropoiesis ; differentiation ; gene switching ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Bone marrow cells from normal adult mice were introduced by microinjection via the placenta into W/Wv genetically anemic fetuses of 11 days' gestation. After birth, erythrocytes were fractionated by fluorescence-activated cell sorting on the basis of antibody binding to a fetal-specific antigen (Ft). Lysates of Ft-positive, i.e., fetal, erythrocytes did not detectably contain hemoglobin of the donor type, as judged from electrophoresis of strain-specific hemoglobin variants. Thus, adult hematopoietic bone marrow cells did not resume fetal differentiation despite their post-transplant maturation in a fetal environment.
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  • 8
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 255-272 
    ISSN: 0192-253X
    Keywords: salivary glands ; pupation stage ; protein synthesis and transport ; prepupal development ; developmentally regulated proteins ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Pulse-labeling experiments of salivary glands from the prepupal stages of development showed selectively high rates of synthesis of a set of low molecular weight proteins (6K-12K). These proteins are stably maintained in the salivary glands during prepupal development and are subsequently transported to the pupation fluid (found between the pupal case and the prepupal cuticle) when pupation occurs. These small polypeptides are very basic with the major components having isoelectric points of 8.6-8.7 and the minor components having isoelectric points of 9.1-9.5. This study shows the continuing function of the salivary glands - specifically, the synthesis and secretion of a set of proteins with a putative role in pupation.
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  • 9
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983), S. 333-339 
    ISSN: 0192-253X
    Keywords: Drosophila ; chromosome ; polyteny ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: A 315 kb walk in the genetically well characterized rosy region of the Drosophila chromosomes permits a molecular analysis of chromosome organization. Polytene chromosome bands in this region range from less than 7 kb to about 160 kb and the level of DNA replication is constant within bands and among bands and interbands. A good numerical and topographical correspondence is found between chromomeric units and genetic units.
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  • 10
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983), S. 355-378 
    ISSN: 0192-253X
    Keywords: courtship ; learning ; biological rhythms ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Reproductive behavior in Drosophila involves a complex series of actions which is perturbed by many different kinds of mutations. Some of the most interesting courtship variants are those originally isolated with respect to disruptions of general learning and memory. Several types of genetically abnormal males have their “conditioned courtship” blocked or attenuated by the learning and memory mutations, some of which, in turn, are known to cause abnormal levels of specific monoamines or cyclic nucleotides. Recent studies of the defective courtship performed by the conditioning mutants involve “mosaic focusing” of the neural tissues affected by the behavioral/biochemical mutations. These experiments address the question of whether there are localized influences of the relevant genetic loci in their control of conditioned courtship, in spite of the fact that the protein products of the genes have a broad tissue distribution. Female responses to courting Drosophila males can also be dependent on the former's prior experiences. This pertains to enhancing aftereffects of prestimulation by the courtship song that is produced by a male; and the same learning and memory mutations, expressed in females, impinge on the normal aftereffects. One element of acoustical communication in courtship is a rhythmic oscillation in a particular component of the song. This short-term behavioral rhythm is altered in males expressing circadian rhythm mutations. To investigate the neural and cellular mechanisms by which these genes act, a mosaic analysis has been initiated on the ganglia affected by a clock mutation in its disruption of the courtship rhythm and of circadian cycles. A molecular isolation and identification of the normal form of this genecalled period - has also begun, in order to probe the locus's structure and function in detail. Such an investigation will include a comparison of the mosaic results with a direct determination of the various tissues in which the gene's product is expressed. In addition, interspecific transfers of the purified period gene will augment the current studies of species-specific features of the rhythmic courtship songs.
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  • 11
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983), S. 425-438 
    ISSN: 0192-253X
    Keywords: polymorphism ; enzyme ; control gene ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: A study was made of environmental and genetic factors affecting the quantity and disposition of the alcohol dehydrogenase (ADH) protein in Drosophila melanogaster. It was found that the amount of enzyme per fly is greatly influenced by the environmental conditions in which it develops. A critical factor is the concentration of yeast in the medium. A high concentration of yeast can double the quantity of ADH. The yeast appears to act through the provision of protein, and the protein to act through the provision of threonine, which is already known to induce ADH in fungi.Various genetic factors affect the quantity of enzyme. Males have more ADH than females. Files homozygous for the Fast allele have more ADH than those homozygous for the slow allele, and the difference is greater in females than in males. One particular line (ve), homozygous for Slow, has approximately half the normal quantity of enzyme, and the quantity segregates with the electrophoretic allele. Lines differ in the relative amounts of ADH in the gut (including Malpighian tubules) and the fat body. In general it seems that slow lines have relatively more enzyme in the fat body. In a cross between ve and a line homozygous to Fast, the difference in tissue distribution segregated with the electrophoretic allele. It is argued, but not demonstrated, that the differences in quantity and tissue distribution are due to nucleotide substitutions in noncoding regions close to, or within, the structural gene.It seems likely that the observed environmental and genetic differences in the quantity and disposition of ADH will influence the relative selective values of the electrophoretic genotypes.
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  • 12
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983), S. 407-424 
    ISSN: 0192-253X
    Keywords: selection ; enzyme ; control-gene ; DNA polymorphism ; Drosophila ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The control of alcohol dehydrogenase (ADH) activity in natural populations of Drosophila melanogaster is chromosomally diverse and due to variation in allotype, enzyme level, and possibly post-translational modification. A comparative study of evolution in Adh structural gene variations with those loci modifying ADH expression has been carried out in large model populations maintained in environments that varied in temperature and food. Broadly based measures of gene expression were obtained as ADH activity and ADH protein level (determined immunologically) from individual flies whose allotype was also determined. The response to selection by “regulatory” or modifier loci compared with ADH allotypes was found to vary with environment, and its direction was not necessarily predictable from the kinetic properties of allele products. Selection for dominance modification of ADH activity in relation to Adh allotype was also observed. Analysis of genotype-environment interaction discerned two main types of response. Two major classes of chromosomal types, identified from restriction endonuclease map variations in a 12-kb region of DNA containing the Adh transcriptional unit, were present in the population. These two types of chromosome were in turn associated with the two types of interaction between genotypes and the environment. The results implicate polylmorphism for the control of genotypeenvironment interaction in populations, a genetically complex unit of selection, and a degree of evolutionary independence between structural and regulatory genes.
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  • 13
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983) 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 14
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983), S. 229-230 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 15
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 129-142 
    ISSN: 0192-253X
    Keywords: glycerol phosphate dehydrogenase ; turnover ; Drosophila ; gene dosage ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: In vivo radiolabeling of Drosophila melanogaster sn-glycerol-3-phosphate dehydrogenase (E.C. 1.1.1.8; GPDH) has been accomplished by microinjection of 3H-leucine into anesthetized flies. Comigration of immunoprecipitated radiolabeled GPDH with purified 14C-labeled GPDH-1 in SDS polyacrylamide disc gels has established the monospecificity of our immunoprecipitation technique. Short-term uptake experiments have demonstrated that maximum radiolabel incorporation of total TCA precipitable protein and immunoprecipitable GPDH-1 occurs within 4 hours postinjection, with GPDH-1 accounting for approximately 1% of the total radiolabeled TCA precipitable protein. In order to develop the parameters for turnover studies of GPDH in Drosophila, a comparative analysis of the rates of synthesis and degradation of GPDH-1 in flies bearing two and three doses of the structural gene have been conducted by the construction of adult flies aneuploid and euploid for the cytogenetic region 25F-26B on the left arm of chromosome II. Short-term uptake studies have demonstrated that the rate of GPDH-1 synthesis in the three-dose flies is approximately 1.58 times that found in the two-dose euploid flies. This value is in close agreement with data obtained for steady-state levels of CRM by rocket immunoelectrophoresis. In contrast, longterm pulse-chase experiments have revealed that rates of GPDH-1 degradation in these aneumploid and euploid flies appear to be identical. These data suggest that the rate of GPDH-1 synthesis in Drosophila is primarily regulated by a tightly linked cis-acting element which appears to act autonomously with respect to gene copy number as well as steady-state GPDH protein levels.
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  • 16
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 165-176 
    ISSN: 0192-253X
    Keywords: X-chromosome inactivation ; digynous triploidy ; mouse ; post-implantation embryo ; late replication ; Cattanach's translocation ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Using BrdU-labeling and acridine orange staining, the behavior of X-chromosome replication was studied in 28 XXX and 19 XXY digynous mouse triploids. In some of these the paternal and maternal X chromosome could by cytologically distinguished. Such embryos were obtained by mating chromosomally normal females with males carrying Cattanach's X chromosome which contains an autosomal insertion that substantially increases the length of this chromosome. In the XXX triploids there were two distinct cell lines, one with two late-replicating X chromosomes, and the other with only one late-replicating X. The XXY triploids were also composed of two cell populations, one with a single late-replicating X and the other with no late replicating X chromosome. Assuming that the late-replicating X is genetically inactive, in both XXX and XXY triploids, cells from the embryonic region tended to have only one active X chromosome, whereas those from the extra-embryonic membranes tended to have two active X chromosomes. The single active X chromosome was either paternal or maternal in origin, but two active X chromosomes were overwhelmingly maternal in origin, suggesting paternal X-inactivation in extra-embryonic tissues.
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  • 17
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 207-214 
    ISSN: 0192-253X
    Keywords: germ line clones ; bithorax lethals ; dominant female sterile mutation ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Three Ultrabithorax (Ubx) alleles and three different deficiencies of the bithorax complex (BX-C) of Drosophila melanogaster have been tested for maternal effects in the germ line. The dominant female sterile technique was used. The Ubx alleles and a deletion of the abdominal region of the BX-C are homozygous viable in germ line clones and show no maternal effects. Two deletions which lack the proximal portion of the BX-C are lethal in the female germ line indicating either that these deficiencies lack genes apart from the BX-C that are necessary for fertility or that there are BX-C genes that are essential for normal maternal germ line function. The significance of the bias in the isolation of only zygotic mutations at the BX-C are discussed with respect to these results.
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  • 18
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 235-245 
    ISSN: 0192-253X
    Keywords: Drosophila ; chitin biosynthesis ; lethalcryptocephal mutation ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Estimation of chitin deposition in the pupal and adult cuticles of adult Drosophila melanogaster during the pupal period is described. The timing of the periods of chitin deposition is compared with that deduced by previous workers using electron microscopy. The hypothesis that lethalcryptocephal mutant homozygotes are unable to evert their cephalic complexes at pupation because of excess chitin deposition is examined. The data obtained show no evidence that the mutation has any effect on chitin deposition.
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  • 19
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982) 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 20
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 283-297 
    ISSN: 0192-253X
    Keywords: Dictyostelium discoideum ; cAMP-unresponsive mutants ; parasexual genetic analysis ; cell differentiation ; chemotaxis to folate and cAMP ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: To find mutants of Dictyostelium discoideum that are unable to respond to exogenous cAMP signals (frigid mutants), amoebae of 218 independent aggregation-deficient mutants were treated in suspension with artificial pulses of cAMP and screened for the capacity to form EDTA-resistant cohesion sites. Eleven frigid mutants were identified and further characterized. Using parasexual genetic techniques, these strains were assigned to five complementation groups (fgdA-E) and the fgd loci were mapped in three linkage groups: fgdA and D in group II, fgdC in group III, and fgdB and E in group VII. Biochemical and physiological experiments with these strains indicated that fgd mutants are of two general types. When starved, strains in groups fgdB, D, and E failed to produce detectable levels of membrane-associated cAMP phosphodiesterase, surface cAMP receptors, or extracellular phosphodiesterase inhibitor, and the cells continued to respond chemotactically to folate. Thus, these strains are probably arrested in the vegetative phase or very early in development. In contrast, strains in groups fgdA and C produced low levels of cAMP receptors and secreted phosphodiesterase inhibitor. Moreover, after starvation, some of these mutants elicited a weak chemotactic response to cAMP. Therefore, unlike the former group of mutants, these strains appear to initiate development when starved, but the process is blocked at an early stage.
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  • 21
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    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 365-365 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
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  • 22
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    Developmental Genetics 4 (1983), S. 1-20 
    ISSN: 0192-253X
    Keywords: gene transfer ; mouse embryos ; genetic engineering ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 23
    ISSN: 0192-253X
    Keywords: catalase ; Drosophila ; development ; turnover ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The ontogenetic and tissue-specific expression of catalase (E.C. 1.11.1.6) has been determined in a wild type strain of Drosophila melanogaster derived from a natural population. Two distinct peaks of activity are observed during development with the first peak occurring in late third instar larvae just prior to puparium formation, and the second and larger of the two peaks occurring during metamorphosis. These peaks of catalase activity are coincident with the two major peaks of ecdysone titer. Of the tissues assayed, larval malpighian tubules, gut, and fat body demonstrated the highest specific activities. Adult abdomen exhibited a two- to three-fold higher specific activity than either head or thorax. Of the abdominal tissues assayed, malpighian tubules and abdominal wall had the highest specific activities. Malpighian tubules were the only sexually dimorphic tissue with respect to catalase activity and are apparently largely responsible for an overall increase observed in female abdominal activity. Catalase-specific CRM levels parallel the enzyme activity levels indicating that these tissue-specific activity differences reflect differences in the rate of accumulation of catalase molecules.Turnover studies employing the catalase inhibitor 3-amino-1,2,4-triazole were conducted on head, thorax, and abdomen of male adult flies. Rates of catalase degradation were similar in the three body segments with a slightly higher rate in abdominal tissue. Therefore the different steady state levels observed largely reflect different rates of catalase synthesis.
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    Developmental Genetics 4 (1983), S. 143-143 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
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  • 25
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    Developmental Genetics 4 (1983) 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
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    Developmental Genetics 4 (1983), S. 185-198 
    ISSN: 0192-253X
    Keywords: maternal effects ; Polycomb locus ; Drosophila ; homoeosis ; Enhancer of Polycomb ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: A mutation or deficiency of the Enhancer of Polycomb (E(Pc)) locus acts as a dominant enhancer of the adult mutant phenotypes of a group of similar homoeotic loci (Polycomb, Polycomblike, extra sex comb, and lethal(4)29). The E(Pc) mutation has a recessive lethal effect, and homo- and hemizygotes die as late embryos or larvae which appear cuticularly normal. E(Pc) also acts as a dominant enhancer of the embryonic homoeotic syndromes associated with Polycomb. Polycomblike, and lethal(4)29 mutations: its effect on the extra sex comb syndrome has not been effectively evaluated. At least for the interaction with Polycomb mutations, evidence is presented that the Enhancer of Polycomb locus has a maternal as well as a zygotic effect, and that its effect on Polycomb expression is not at the level of transcription. We suggest that the Enhancer of Polycomb locus acts specifically to regulate the activities of this set of homoeotic loci, and that E(Pc) recessive lethality results from noncuticular homoeotic defects which arise as a consequence of their reduced activity. In the context of this hypothesis, no present data allow us to distinguish whether Enhancer of Polycomb is a nonhomoeotic locus regulating the function(s) of Polycomb and related genes or is itself a homoeotic locus.
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  • 27
    ISSN: 0192-253X
    Keywords: chimera ; cell interactions ; sex reversed ; sex determination ; melanocyte ; intersex ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The manufacture of mammalian chimeras by aggregating embryos of different genetic constitutions makes possible the study of the genetic control of cellular interactions during embryonic development. Several different chimeric combinations have been made to study the role of the sex-reversed mutation in gonadogenesis and in gametogenesis. Sex reversed directs the gonad to become a testis and thus renders a SxrXX mouse sterile since gonocytes with two X chromosomes cannot complete gametogenesis in a testis. However, SxrXX gonocytes in the ovary of a female chimera become normal oocytes. The competitive interactions of genetically different melanoblasts in populating hair follicles and of primordial germ cells in populating the gonad have been revealed in chimeras. Chimeras have also been used to rescue inviable teraploid embryos and to permit teteraploid cells to display their differentiative capacities in normal tissue environments. We conclude that the genotype affects the capacity of cells to elaborate and to respond to inductive stimuli at each step in differentiation. The fine tuning of cellular interactions becomes apparent in chimeras made from embryos of different genotype.
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  • 28
    ISSN: 0192-253X
    Keywords: alcohol dehydrogenase ; Drosophila ; evolution ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The gene coding for alcohol dehydrogenase (Adh) in Drosophila melanogaster maps to 2:50.1 on chromosome arm 2L. It is expressed in both larvae and adults, coding for an abundant enzyme that plays a role in the detoxification of primary and secondary alcohols. In larvae the gene is most abundantly expressed in the fat body and gut. We have recently shown [49] that the major Adh transcripts differ in larvae and adults, the major adult transcript being initiated from a promotor several hundred pairs 5′ to the promotor from which the major larval transcript is initiated. However the coding region of the “larval and adult” mRNA are identical. We discuss recent studies of the transcriptional organization Adh and compare the structure of this gene in D. melanogaster with that in other species of Drosophila. The entire Adh gene and its surrounds has been sequenced from four species of Drosophila [45,48]. This data has been used not only for the study of phylogenetic relationships, but also of the types of sequence variation seen between species. The constraints on mutational change, especially with respect to codons, will be discussed.
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  • 29
    ISSN: 0192-253X
    Keywords: retrovius ; chromosomal evolution ; feline genetics ; somatic cell genetics ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: A combination of technical advances (most notably heterologous cell fusion, high resolution G-banding, and molecular cloning) has contributed to an accelerated advance in genetic analysis in mammals. The present human genetic map contains over 400 gene assignments and the map is growing rapidly as each new molecular clone or immunological reagent is developed. In our laboratory, we have developed a panel of rodent X human somatic cell hybrids that have been utilized in chromosome assignment of several classes of genes including oncogenes (ras, raf) and endogenous human retroviral sequences (ERVL, 2, etc). Using similar techniques, a biochemical genetic map of the domestic cat has been derived. The cat has 19 chromosome pairs and, to date, 40 genes have been mapped to 16 linkage or syntenic groups. Comparison of linkage relationships between homologous enzymes has revealed a striking conversation of chromosomal linkage association between cat and man. A comparison of syntenically homologous, highly extended high resoultion G-banded chromosomes between the two mammalian families revealed that 20-25%, by length, of the human karyotype can be precisely aligned (chromomere to chromomere) between cats and man despite the evolutionary divergence of the species nearly 80 million years ago.Moderately repetitive families of retrovirus-related DNAs exist within the feline and the human genomes. We have isolated molecular clones of several members of the feline RD-114 retrovirus family from a genomic library of normal cat cellular DNA. The endogenous sequences analyzed were similar to each other in that they were colinear with RD-114 proviral DNA, were bounded by long terminal redundancies, and conserved many restriction sites in the gag and pol regions. Several sequences were apparently deleted, relative to the previously characterized inducible RD-114 genome. The env regions of a number of endogenous RD-114 sequences examined were substantially deleted or diverged; a subset of these sequences contained information at the position of the env region that was not homologous to inducible RD-114. The RD-114 virogenes were dispersed to several cat chrosomes that were localized using a panel of rodent x cat somatic cell hybrids. A comparison of the genetic properties of endogenous human retroviral sequences revealed several similarities between the human and feline status of endogenous retroviruses.
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    Developmental Genetics 3 (1982) 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
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  • 31
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    Developmental Genetics 3 (1982), S. 7-23 
    ISSN: 0192-253X
    Keywords: gene expression ; superoxide dismutase ; Zea mays ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Immunoassays for the cytosolic and mitochondrial superoxide dismutases (SOD) of maize were developed and used to study the expression of these proteins in the maize seedling. The genetically distinct proteins, SOD-3 and SOD-4, are preferentially expressed in the scutellum, comprising approximately 1% of the total water-soluble protein of that tissue. SOD-2, SOD-3, and SOD-4 are synthesized in the scutellum during early sporophytic development, probably on cytosolic ribosomes. Two-dimensional gel electrophoresis of crude scutellar extracts indicates that significant changes occur in the protein composition of the maize scutellum following seed imbibition. Using the immunoassays, a maize line exhibiting a significant reduction in cyanide-sensitive SOD protein was identified.
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  • 32
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    Developmental Genetics 3 (1982) 
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    Keywords: Life and Medical Sciences ; Genetics
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  • 33
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    Developmental Genetics 3 (1982), S. 177-177 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
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  • 34
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    Developmental Genetics 3 (1982), S. 179-196 
    ISSN: 0192-253X
    Keywords: alcohol dehydrogenase ; regulatory ; mutant ; mutable alleles ; organ-specific ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Three new mutant alleles of maize alcohol dehydrogenase-1 (Adh 1) were recovered following allyl alcohol selection of pollen. Each is altered in quantitative, organ-specific, regulatory properties. All mutant sites act in cis to the structural gene component. One mutant arose spontaneously, one followed indirectly from irradiation with high Z accelerated particles, and one was induced by an autonomous mutator system. Each mutant is assessed in three organs by utilizing ADH allozyme ratios that were quantified at the level of ADH enzyme activity and either [3H]-Leu incorporation into newly synthesized ADH 1 subunits or direct protein determinations. One mutation simultaneously raises Adh 1 expression in one organ and lowers it in another, another affects expression in one organ only, and another is extremely underexpressed in all organs but is unstable. This unstable allele has generated derivative mutant alleles that have less or zero ADH expression. We do not yet know whether or not coding sequences are involved in these mutants. We conclude that information for organ specificity and quantitative behavior resides near or within Adh 1 coding sequences.
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  • 35
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    Developmental Genetics 4 (1983), S. 99-115 
    ISSN: 0192-253X
    Keywords: differential allelic expression ; Zea mays ; isozyme ; endosperm ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The timing of gene expression in the endosperm of developing F1 maize kernels was investigated. Zymogram analysis revealed the presence of maternally derived allelic gene products on all days investigated, but activity of paternally derived allelic gene products is not detectable until days 6-8 postpollination, depending on the particular cross used and the enzyme investigated. This pattern holds true for eight different isozymes of five different enzyme systems, including catalase, alcohol dehydrogenase, glutamate-oxaloacetate transaminase, endopeptid́ase, and aminopeptidase. An increase in specific activity for catalase, alcohol dehydrogenase, and endopeptidase correlates precisely with the day of visualization of the paternally derived allelic gene product on the zymograms. Rocket immunoelectrophoresis confirms a dramatic increase in catalase and alcohol dehydrogenase protein levels on the day the paternally derived allelic gene product is first detected on zymograms. Appropriate crosses utilizing three different allelic variants revealed the presence of enzyme of maternal plant origin within the endosperm prior to day 6 postpollination.Maize kernels were cultured in vitro on an agar-based medium as early as 3 days postpollination. Using medium supplemented with actinomycin D or cycloheximide, it was possible to localize the critical time periods for transcription and translation of the paternally derived allele in the F1 hybrids. For aminopeptidase (AMP-1, AMP-3) and endopeptidase (ENP-1), transcription occurs as early as 3-4 days postpollination, and translation of the transcripts starts at about 4-5 days postpollination. Although the evidence is indirect, it is likely that the maternally derived allele of the F1 kernels is activated (ie, begins transcribing) synchronously with the paternally derived allele during this early developmental time period.
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    Developmental Genetics 4 (1983), S. 159-165 
    ISSN: 0192-253X
    Keywords: trisomy ; monosomy ; aneuploidy ; chimeras ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Mouse trisomy 15 ↔ 2n aggregation chimeras have been produced and analyzed at 19 days of gestation. We have found that these chimeras are viable and in most instances normal in external appearance, unlike trisomy (Ts)-15 embryos which are severely growthretarded and die midway through gestation. Trisomic cells were found in all tissues of fetal chimeras, with proportions not significantly different from those of the controls in kidney, heart, liver, and brain, but significantly reduced in thymus and spleen. Ts-15 cells do not, therefore, exhibit a proliferative advantage during fetal development of tissues susceptible to Ts-15-related lymphoid malignancies. However, the presence of Ts-15 cells in the placenta may be associated with placental overgrowth. One fetus containing a monosomy 3 cell population was also observed, the first term fetal chimera with monosomic cells that has been detected.
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    Developmental Genetics 4 (1983), S. 211-227 
    ISSN: 0192-253X
    Keywords: Drosophila melanogaster ; geotaxis ; phototaxis ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The use of Drosophila as an organism in which to study aging has been limited by the fact that few biomarkers of aging exist in the adult. In this paper we examine behavior loss relative to longevity in wild-type populations maintained at 22°C and 29°C to determine whether behavior loss - that is, loss of ability to perform certain innate behavioral responses within a defined test interval - can be used as biomarkers of aging. We find that under controlled conditions behavior loss can be used as a landmark of aging in populations maintained at either 22°C or 29°C. The ability to perform normal geotactic and phototactic responses is lost during the reproductive phase of the adult populations, whereas motor activity is not lost until well into the death phase. We feel that the use of behavior loss, together with other parameters of longevity in Drosophila, will allow comparisons to be made between different strains or between different environmental conditions to test their effect on aging. In the companion paper we demonstrate the use of behavior loss to identify a mutation which may accelerate the aging process.
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    Developmental Genetics 3 (1982) 
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    Keywords: Life and Medical Sciences ; Genetics
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  • 39
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    Developmental Genetics 4 (1983) 
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    Keywords: Life and Medical Sciences ; Genetics
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  • 40
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    Developmental Genetics 4 (1983), S. 69-76 
    ISSN: 0192-253X
    Keywords: Polysphondylium ; cellular slime mold ; microcysts ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Mutants were selected that are incapable of differentiating microcysts, a resting stage formed in response to high osmotic conditions. In the selection procedure amebae that failed to encyst were removed by flotation in 46% Percoll. Genetic crosses among 15 mutant strains were made by means of the macrocyst sexual cycle. Eleven of the strains mapped to three loci. Mutations at two of these loci (cysA and cysB) produced no observable alteration in the aggregation-fruiting pathway, although one set of strains altered at the cysA locus carried defects at a second unlinked site which blocked aggregation. The single strain that defined the third locus (cysC) is aggregateless. These results confirm the conclusion that there are several genes whose function is essential to microcyst development and is exclusive to this pathway. It remains uncertain whether there are other genes whose action is crucial to both encystment and to aggregation/fruiting.
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  • 41
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    Developmental Genetics 4 (1983), S. 117-127 
    ISSN: 0192-253X
    Keywords: Physarum polycephalum ; differentiation ; food supply ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The effect of food supply on the onset of asexual and sexual plasmodium formation in Physarum polycephalum was studied. Asexual differentiation occurs readily in amoebae carrying the matAh mating type allele. The density at which these amoebae begin to differentiate is influenced by the ind locus, which controls the production of a diffusible inducer. The alleles ind-1 and ind-2 are known. Strains carring the ind-1 allele begin plasmodium formation at a low amoebal density (rapid differentiation), while strains carring the ind-2 allele differentiate at a higher amoebal density (slow differentiation). The onset of differentiation is characteristic of the strain and did not change with a 20-fold variation in the number of food bacteria available. Sexual differentiation occurs between compatible amoebal strains. For a given pair of amoebal strains the onset of plasmodium formation occurs at a characteristic cell density that is determined by the genetic backgrounds of the strains. The ind locus is one of the genes that influences this cell density. Plasmodia are formed at a lower cell density in crosses involving compatible amoebae carrying the ind-1 allele than they are in crosses with strains carrying the ind-2 allele. As was found for asexual differentiation, an approximate 20-fold variation in the food supply did not affect the initiation of sexual plasmodium formation. These results suggest that in most cases starvation does not trigger the differentiation of amoebae into plasmodia. The time of onset of plasmodium formation is determined largely by genetic factors.
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  • 42
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    Developmental Genetics 3 (1982), S. 69-89 
    ISSN: 0192-253X
    Keywords: female sterility mutations ; fusome ; incomplete cytokinesis ; interconnected sibling cells ; ongenesis ; ovarian tumor genes ; polytene chromnsomes ; pseudonurse cells ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: A comparative cytological study was made of oogenesis in flies carrying various mutant alleles of the female sterile gene otu. It resides at 22.7 on the genetic map and within subdivision 7F of the cytological map of the X-chromosome. Each of the five ethyl methane sulfonate-induced mutations observed falls into one of three classes. In class 1, most mutant ovarioles lack germ cells; in class 2, most mutant ovarioles contain tumorous chambers; and in class 3 mutants, chambers occur that possess defective oocytes. The otu2 allele belongs to class 1; otu1 to class 2; and otu3, otu4, and otu5 to class 3. The mutations have no effects upon female viability or upon the viability and fertility of hemizygous males. Heterozygous females are fertile and have cytologically normal ovaries. In otu5 homozygotes, all ovarioles contain egg chambers, but oogenesis is prematurely terminated to produce a pseudo-stage 12 oocyte. Ovarioles from otu3 and from otu4 homozygotes contain both ovarian tumors and oocytes. Pseudonurse cells (PNC), which are cystocytes that have stopped dividing and have entered the nurse cell mode of development, are also abundant. PNCs contain polytene chromosomes. Since the homologs are paired, each nucleus has the haploid number of chromosomes. In chambers lacking an oocyte, the number of PNCs is less than the normal number of nurse cells. In chambers containing an oocyte, the number of accompanying nurse cells may be 15, or above or below normal. In vitellogenic chambers, the chromosomes in the nurse cells connected directly to the oocyte are more expanded than those in more distant nurse cells. The KA14 deficiency lacks the plus allele of otu. KA14 heterozygotes are fertile and have cytologically normal ovaries. When females carry KA14 and otu1, otu3, otu4, or otu5, 80% of their ovarioles are agametic. When females carry otu2 and one of the other mutant alleles, the ovarioles proceed further in development. So otu2 produces a product that has a beneficial effect on the test allele. When two different otu alleles are combined in a single fly, the phenotype of the hybrid ovary usually most resembles that of the ovary homozygous for the “stronger” allele (the otu mutant that allows oogenesis to proceed farthest). The results indicate that the product of the otu+ locus functions at least three different times during oogenesis; first to permit oogonia to proliferate, second to control the division and differentiation of germarial cystocytes, and third to facilitate the normal growth of the ooplasm. The gene product appears to be required in higher concentrations at each developmental period. The lesions produced by the mutations are thought to interfere with the stability or functioning of the gene product, and the ovarian phenotype produced by a given genotype depends upon the concentration of functional gene product available to the germ cells.
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    Developmental Genetics 3 (1982), S. 103-113 
    ISSN: 0192-253X
    Keywords: Drosophila melanogaster ; Polycomb ; homoeotic mutation ; determination ; maternal effect ; embryogenesis ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: When heterozygous, dominant mutant alleles of the Polycomb locus are associated with a variety of adult homoeotic effects. Zygotes homozygous for these alleles die as late embryos showing homoeotic transformation of head, thoracic, and abdominal segments. This study shows that embryos homozygous for Pc3 are more extreme than those homozygous for Pc1 or Pc2. Moreover, Pc1/Pc3 heterozygotes are more extensively transformed if their mothers were Pc3/ + than if they were Pc1/ +; this effect does not depend on zygotic genetic background and must be maternal in nature. Embryos homozygous for Pc3 are less extreme if they arise from Pc3/ + / + than from Pc3/ + mothers. These results strongly suggest that the Polycomb locus acts maternally as well as zygotically to affect early determinative decisions.
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  • 44
    ISSN: 0192-253X
    Keywords: B cell development ; immunoglobulin M ; B cell tumor ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Tumors of B lymphocyte origin have been used as models for normal B cells “frozen” at particular stages of their development. Surface properties, amount, and intracellular location of immunoglobulin and the synthesis of J chain have all been used as indicators of developmental stages. Each requires special techniques or yields data that are difficult to compare from one experiment to the next. For these reasons, we have developed a metric for B cell development that is simple to perform and allows quick quantitative comparisons of cell lines.It has recently been established that the membrane (μm) and secreted (μs) forms of the IgM heavy chain differ at their extreme carboxy termini. The two proteins differ slightly in size and are easily distinguished when they are compared without their carbohydrate on sodium dodecyl sulfate (SDS) polyacrylamide gels. We have examined four mouse tumors derived from the B lymphocyte lineage whose phenotypes resemble late pre-B cells (internal μ only; uninduced 70Z/3), small B lymphocytes (high levels of surface IgM; LPS-induced 70Z/3, WEHI 231), lymphoblasts (both membrane and secreted IgM; WEHI 279.1), and plasma cells (copious IgM secretion; MOPC 104E). Despite the fact the 70Z/3 and WEHI 231 secrete no detectable IgM, all of the tumors synthesize at least intracellular forms of both μm and μs. The proportion of μm is stable and is characteristic of each tumor. The 70Z/3 cells and WEHI 231 cells synthesize about 75% of their total μ as μm; WEHI 279.1 cells synthesize about 30% and MOPC 104E cells about 5% of their total μ as μm. The population of LPS-stimulated B lymphocytes shows a similar progression during its differentiation. The proportion of μm correlates with other developmentally regulated parameters (Fc receptor, Ia and plasma cell antigen levels, and J chain) and can be used as a simple metric for comparison with developing B lymphocytes and determination of the developmental stage of a B cell tumor.
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    Developmental Genetics 3 (1982), S. 143-154 
    ISSN: 0192-253X
    Keywords: imaginal neurogenesis ; visual development ; genetic mosaics ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The neural phenotype of an imaginal disc degenerate mutant l(1)d deg-3 was studied in histological sections. The mutant larvae showed severe abnormalities in the imaginal neural development. Gynandromorphs, which are composed of genetically mutant and nonmutant cells, were generated and analyzed as late larvae. The results of mosaic analysis were consistent with l(1)d deg-3 gene acting autonomously in the imaginal disc and imaginal neural cells. The optic lobe development patterns observed in the larval mosaics provided evidence for an eye disc-optic lobe interaction during the late third instar larval stage.
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  • 46
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    Developmental Genetics 4 (1983), S. 199-210 
    ISSN: 0192-253X
    Keywords: aging ; Drosophila ; behavior ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The question as to the role that genes play in determining life-span is essentially unresolved. Although it is well documented that genotype influences longevity, this is no way demonstrates that life-span is genetically determined. In the present study we examine five temperature-sensitive mutations for their effect on the aging process. At the permissive temperature (22°C ), the longevity of each mutant strain is comparable to that of wild type. However, at the restrictive temperature (29°C ) the life-span of these mutants is severely curtailed. Using behavior loss as a landmark of adult physiological age, we examined each of these strains for its pattern of behavior loss relative to longevity, and compared each to a wild-type strain. In four of the mutations the pattern of behavior loss relative to longevity was severely altered at one or both temperatures. However, one strain, adl-16tsl displayed a pattern of behavior loss that was indistinguishable from wild type at both 22°C and 29°C. At 29°C not only was the longevity decreased, the pattern of behavior loss was also compressed into a shorter time period. The compression of the pattern of behavior loss was proportional to the reduction in life-span. Thus it appears that this mutation, adl-16tsl, may accelerate the normal aging process when placed at 29°C. The potential utility of these types of mutants for studying the aging process is discussed.
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  • 47
    ISSN: 0192-253X
    Keywords: Drosophila ; small heat-shock protein genes ; ecdysterone ; regulation ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The four small heat shock protein genes of Drosophila are tightly linked at the level of DNA, and are coordinately regulated. In cultured cell lines their expression is induced by high temprature shock and by physiological doses of ecdysterone. In vivo, small heat shock gene expression is developmentally regulated. Using recombinant DNA clones we have characterized and compared small hsp gene induction in response to the two independent stimuli.
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    Developmental Genetics 3 (1982), S. 329-345 
    ISSN: 0192-253X
    Keywords: Drosophila embryo ; mutation ; myogenesis ; fibrillogenesis ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The I(1)fdg mutation demonstrates two separate phases of lethality, depending on developmental conditions. At 32-33°C, an embryonic lethality is expressed whereas at lower temperatures a larval-pupal lethality is observed. This larval-pupal lethality characteristically produces noncondensed, curved puparia, and since the contraction of the pupa depends on strong muscular contraction, this phase of lethality implicates some involvement of abnormal musculature. The embryonic expression of I(1)fdg at 32-33°C is the subject of this study. In these embryos, which are alive but immobile (incapable of hatching), the fibrillar organization and fiber morphology of the somatic musculature varies from being apparently normal to being grossly abnormal. While the abnormalities appear as unusual distributions of fiber organelles, abnormal convolutions of the muscle fibers, and disorganizations of fibrillar components, it seems most probable that the underlying defect ultimately responsible resides in some system essential for Z body alignment and sarcomere formation. Accompanying the embryonic lethality, certain abnormalities in midgut development are observed which at present do not appear to be related to the defects observed in the somatic muscle.
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    Developmental Genetics 3 (1982), S. 347-363 
    ISSN: 0192-253X
    Keywords: Drosophila melanogaster ; muscle defect ; genetic mosaics ; allelic variability ; intragenic complementation ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The recessive X-linked mutation erect wing (ewg), in Drosophila melanogaster, was characterized as a flightless behavioral mutant which specifically lacked the dorsal longitudinal flight muscles [1]. This mutation was mapped distal to the X chromosomal locus yellow, and further to the cytological segment 1 A 1 to 1 B2-3 [2]. Several lethal complementation groups have been mapped to this interval [3]. Our complementation tests show that ewg is allelic to one lethal complementation group in the region 1 A 1 to 1 B2-3. A further analysis of ewg and several lethal alleles isolated at this locus was undertaken in the present investigation. Most of the lethal alleles at this locus lead to a late embryonic or early larval lethal phase, indicating that the ewg+ gene product is necessary for the development of more than just the dorsal longitudinal flight muscles. Intragenic complementation was observed for some of the ewg lethal alleles. Genetic mosaics with ewg lethal alleles showed that mutant cell clones in cuticular structures are viable. Mosaic analysis is consistent with a mesodermal defect associated with the locus.
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    Developmental Genetics 4 (1983), S. 31-48 
    ISSN: 0192-253X
    Keywords: B cell development ; IgM ; mouse ; tumor metastasis ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The regulation of IgM expression was studied in clones derived from a murine B lymphocyte cell line, WEHI279.1. During normal B cell development IgM heavy chain synthesis increases concomitantly with heightened IgM secretion and reduced cell-surface IgM. However, in these subclones, the levels of membrane-bound and secreted IgM were regulated independently of one another. The amount of IgM secreted by the cells was tightly coupled to the amount of heavy chain synthesis, suggesting that the major control of secretion is pretranslational. Surface IgM exhibited a more complex regulation, with both pre- and posttranslational components. Variation in the expression of both forms of IgM occurred at high frequency. Although IgM expression follows a unidirectional pathway in nontransformed cells, the variability in these tumor cells was reversible and cellautonomous. High levels of phenotypic variability may be important in the ability of transformed cells to escape the immune response.
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    Developmental Genetics 4 (1983), S. 77-97 
    ISSN: 0192-253X
    Keywords: behavioral mutation ; Drosophila ; flightlessness ; temperature sensitive ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Mutations in 13 genes with temperature-sensitive (ts), flightless phenotypes have been examined. All hop and fly well when raised at the permissive temperature, but fly poorly, or not at all, when raised at the restrictive temperature. The mutations were divided into three groups on the basis of their temperature-sensitive periods (TSPs) for flightlessness. The TSPs for mutations at five loci, fli-C1, D1, E1, I1, and shak A1, in the first group are confined to 24 to 48 hr interval during early pupal development. Mutations in the second group, including eag101, fli B1, and futs1 have continuous TSPs 3 to 4 days in length, extending from late larval through the early pupal stages. The flight TSPs for mutations in the third class, including fli J1, fli K2, flrd H3, and flrd N1, are almost continuous, and span most of the larval and pupal periods. Many of the mutations have pleiotropic phenotypes, including semilethality and lethality, and wing posture and cuticle abnormalities, with discernible TSPs. One of the more intriguing pleiotropic phenotypes is the ts optomotor response exhibited by fli J2, the TSP for which extends from late larval through late pupal stages.
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  • 52
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    Developmental Genetics 4 (1983), S. 129-141 
    ISSN: 0192-253X
    Keywords: cytokin mutant ; habituation ; Nicotiana ; tissue culture ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Cultured leaf tissues of Nicotiana tabacum L. cv. “Havana 425” normally require an exogenous source of cytokinin for rapid growth; stem-cortex tissues do not - ie, they exhibit the cytokinin-habituated phenotype. We found that plants regenerated from cloned cortex and leaf tissues from one particular plant differed in leaf-tissue phenotype: Leaf tissues derived from leaf cells exhibited the normal, nonhabituated phenotype, whereas leaf tissues derived from cortex cells were cytokinin-habituated. This difference in leaf phenotype was not found using leaf and cortex cells from six other donor plants. The inheritance of the habituated leaf trait was studied in tissues from cortex-derived plants and hybrids between these plants and normal plants. F1 hybrids were intermediate between the parental types in degree of habituation. No differences were found between reciprocal hybrids. These results suggest that the habituated leaf trait is an incompletely dominant, nuclear trait. Both parental and intermediate phenotypes were recovered in the F2 progeny. The frequency of habituated leaf progeny in the F2 and backcross populations provide evidence that the trait is regulated at a single genetic locus.
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  • 53
    ISSN: 0192-253X
    Keywords: dedifferentiation ; Dictyostelium ; aggregation ; mutant ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: During slime mold development, cells acquire the capacity to rapidly recapitulate morphogenesis in roughly a tenth the original time. When developing cells are disaggregated and refed, they completely loss this capacity in a rapid and synchronous step referred to as the “erasure event.” The erasure event sets in motion a program of dedifferentiation during which developmentally acquired functions are lost at different times. In this report, we describe the phenotype of HI4, which is a mutant partially defective in the dedifferentiation program but normal in all aspects of growth, morphogenesis, and rapid recapitulation. HI4 cells progress through the erasure event, losing in a relatively normal fashion (I) the capacity to rapidly recapitulate later stages of morphogenesis, (2) the capacity to release a cAMP signal, and (3) the capacity to respond chemotactically to a cAMP signal. However, erased HI4 cells abnormally retain the capacity to rapidly reaggregate, even though they have lost chemotactic functions. Erased HI4 cells also abnormally retain EDTA-resistant cohesion (contact sites A) and the surface glycoprotein gp80. It appears that erased HI4 cells rapidly reaggregate owing to random collisions followed by tight cell cohesion.
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  • 54
    ISSN: 0192-253X
    Keywords: Neurogenesis ; D. melanogaster ; Gene cloning ; Molecular genetics ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Genetic analysis has suggested that neurogenesis in D melanogaster is under the control of a small number of genes. We have initiated a molecular study of the genes involved in this developmental event and started our analysis with the Notch locus, which is one of the best characterized loci in D melanogaster in terms of its genetic structure and developmental effects. In this paper we report on the molecular characterization of the Notch locus.We describe the molecular cloning of Notch and present evidence that the entire locus is defined by approximately 40 kb of genomic DNA. The transcriptional activity of these sequences during development has been examined and the results indicate that an approximately 10.5-kb-long poly A+ RNA is essential for wild type Notch activity. Mapping of this RNA within the physical map of Notch indicates that it is the processed product of an approximately 40-kb primary transcription unit spanning the entire Notch locus. More detailed analysis of the 10.5 kb RNA localizes several exons and identifies a small repetitive sequence that seems to be present in the mature Notch transcript. Structural details of a selected number of Notch locus mutations are presented and discussed. Preliminary data on the molecular structure of Notch-homologous DNA sequences in closely related species are also presented.
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  • 55
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    Developmental Genetics 4 (1983), S. 313-332 
    ISSN: 0192-253X
    Keywords: mRNA structure ; initiation of protein synthesis ; ribosome gel electrophoresis ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: A method is described for the experimental determination of the secondary structure of RNA using enzymatic cleavage data coupled with computer analysis. The structure-specific enzymes S1 nuclease and cobra venom ribonuclease are used to locate nonpaired and basepaired nucleotides, respectively. Computer techniques that utilize the enzymatic susceptibility information to generate a minimum free-energy structure are used to obtain secondary structure models. A second method, using acrylamide-agarose gel electrophoresis, is described for the determination of the relative protein synthesis initiation rates of endlabeled eukaryotic mRNAs. These methods are applied to the rabbit globin mRNAs as an example of a general approach for relating mRNA structure and function. A discussion of the role of messenger RNA structure in the regulation of translation is included with an emphasis on studies of development.
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  • 56
    ISSN: 0192-253X
    Keywords: marine molluscs ; heterozygosity ; growth ; selection models ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: We examine several models that may account for the observation that in populations of marine molluscs in general, and of the American oyster (Crassostrea virginica) in particular, the growth of an individual is related to its degree of heterozygosity and, also, that the number of heterozygous individuals in the population is less than expected on the assumption of random mating and no selection. We classify these models into nonselective, selective, and mixed models. We conclude that mixed models are the most likely to apply to real populations, but cannot exclude selective models. Nonselective models appear least likely. Current evidence favors a model that assumes that heterozygotes enjoy a fitness advantage as adults, primarily because of their faster growth, and that the lower numbers of heterozygotes in the population result from some form of nonrandom fertilization. One possible source of nonrandom fertilization is variation in the time of spawning of individuals due to differences in body size.
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  • 57
    ISSN: 0192-253X
    Keywords: Drosophila ; electrophoretic variation ; quantitative variation ; ecology ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Electrophoretic variation at three enzyme loci-alcohol dehydrogenase (Adh), glycerophosphate dehydrogenase (Gpdh), triosephosphate isomerase (Tpi)- is compared in Australian Drosophila melanogaster populations at three levels of spatial heterogeneity; among breeding sites, within populations, and between populations at the geographic level. Heterogeneity at the breeding site level greatly exceeds that among adults within populations, indicating greater intermixing at the mobile adult stage than at the developmentally immature and less migratory larval stage. Heterogeneity at the microspatial level is large relative to the geographic level at two of these loci.Spatial patterns of variation in ecological phenotypes are also considered. It is argued that electrophoretic variants may contribute little to an understanding of this quantitative variation, and that a more useful approach in ecological genetics is to consider ecological phenotypes as primary data.
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  • 58
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    Developmental Genetics 3 (1982), S. 41-51 
    ISSN: 0192-253X
    Keywords: Artemia ; histone synthesis ; histone genes ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The synthesis of histones and presence of histone mRNA sequences in embryos and larvae of the brine shrimp, Artemia, were investigated. Radiolabeling of proteins synthesized in vivo followed by electrophoretic and fluorographic analysis confirmed the prediction that histone synthesis is coordinated with the wave of DNA replication in newly hatched larvae. No histone synthesis occurs during development of encysted embryos. Hybridization of cloned Artemia histone gene DNA to total cell RNA indicated that dormant encysted embryos do not contain “masked” messenger RNA.
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  • 59
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    Developmental Genetics 3 (1982), S. 91-102 
    ISSN: 0192-253X
    Keywords: hyperthermia ; heat shock ; phenocopy ; teratogenesis ; morphogenesis ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: We have for some years been making use of phenocopies in Drosophila, as induced by heat shock, as tools for studies of the molecular events in morphogenesis [18, 21, 22]. In this paper, we have brought together some accumulated information on the conditions for phenocopy production, on a temporal sequence of sensitivity to induction, and on the nature of many of the morphogenetic abnormalities that can be induced. In general, the induction of phenocopies by heat shock requires conditions drastic enough to turn off transcriptional activities but not extreme enough to prevent recovery. This situation is most easily achieved in pupal stages where heat resistance is high, but even in this range, resistance varies with the stage of development.The phenocopies described resemble, for the most part, mutants that affect structures derived from epithelial differentiation or muscle development.
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  • 60
    ISSN: 0192-253X
    Keywords: tumorous and nontumorous genotypes ; DNA amplification ; repetitive DNA ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The possible relevance of changes in amounts of highly repetitive DNA sequences for plant differentiation and dedifferentiation processes has been suggested in several cases. Data are lacking however on (1) the genetic control of these phenomena and (2) cause-effect relationships between DNA amplification and specific ontogenetic patterns.The present study was carried out on a Nicotiana genetic system consisting of the tumorous amphidiploid N glauca X N langsdorffii, a nontumorous mutant of it, their F1, and a backcross to the tumorous parent. Backcross segregation ratios were shown to be compatible with a “single gene” hypothesis, the F1 plant being nontumorous but showing a low percentage of tumors induced by wounds, 6-azauracil or X-rays.In vitro studies of excised pith tissue grown on Linsmaier and Skoog medium for different periods of time showed the presence, confirmed by cytological analyses, of amplification of highly repetitive sequences only in the nontumorous stock, as judged by reassociation experiments in the first 24-96 hours of culture. CsCl analytical ultracentrifugation of those sequences showed the appearance in the same stock of a heavy DNA satellite (density = 1.721 gm/ml), whose presence was also confirmed by derivative melting curves.Amplification seemed to be essential for the initiation of cell division, which was completely inhibited in the nontumorous genotype and partially influenced in the F1 by incorporation during the critical period (24-96 hours of the primary explant) of 5-bromo-2′-deoxy-uridine.The results are discussed in terms of an hypothesis of an integrated gene-controlled, hormone-mediated regulatory system of cell proliferation involving changes in target repetitive DNA sequences.
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  • 61
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    Developmental Genetics 3 (1982), S. 115-128 
    ISSN: 0192-253X
    Keywords: Drosophila melanogaster ; polygenic variation ; pattern formation ; wing veins ; campaniform sensillae ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: This study was designed to measure the degree of correlation between vein formation and the specification of campaniform sensillae positions in the wing of Drosophila melanogaster. The campaniform sensillae are sensory organs placed at various locations on the wing. Those on the third longitudinal vein (L3) were the focus of this analysis. The system of polygenic modifiers of vein length is comparatively simple, as shown in whole chromosome assays of selected lines. This variability provides a sensitive method of altering vein-forming ability and of assessing correlated changes in other parts of the vein pattern. In selection lines of veinlet, sensillae were displaced toward the base of the wing as vein length decreased by distal loss of vein material. Changes in the amount of vein were, however, not directly proportional to changes in sensillae positions. The more distal sensillae were shifted the largest amount. In the mutant tilt, in which reduced L3 vein-forming competence results in subterminal gaps, distal campaniform sensillae were almost completely eliminated. The remaining sensillae were shifted toward the base of the wing where vein formation is normal. The placement of sensillae therefore appears to be sensitive to the same underlying determinants involved in vein-forming competence.
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  • 62
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    Developmental Genetics 3 (1982), S. 155-163 
    ISSN: 0192-253X
    Keywords: shiverer mouse ; myelin ; myelin basic protein ; myelination ; proteolipid protein ; sciatic nerve ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The central nervous system of the shiverer mouse is known to be severely deficient in myelin. Animals heterozygous for this autosomal-recessive mutation were crossed, and the myelin proteins were examined in the brains and spinal cords of shiverers and unaffected littermates among the offspring. In the brains and spinal cords of nine of the 14 unaffected littermates examined, the quantities of the myelin basic and proteolipid proteins were lower than normal. Furthermore, in the brains of heterozygotes 33 to ∼ 150 days old, the myelin basic and proteolipid proteins were reduced in amount, compared to wild-type controls; the myelin basic protein was also present in subnormal amounts in the spinal cords from heterozygous animals at the ages of 17 to 150 days. More severe reductions in the quantities of the myelin proteins were observed in central nervous system tissue from homozygous shiverer mice, and the quantity of the myelin proteolipid protein in the central nervous system of the shiverer mouse, expressed as a ratio to the control value at each age, underwent a developmental decline. In heterozygotes, as well as shiverers, the peripheral nerves were also deficient in the P1 and Pr proteins, which are the same as the basic proteins in rodent central nervous system myelin. The findings regarding heterozygotes suggest that the defective primary gene product in the shiverer mouse could be the myelin basic protein itself or a protein required for a rate-limiting step in the processing of the myelin basic protein.
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  • 63
    ISSN: 0192-253X
    Keywords: urate oxidase ; 20-hydroxyecdysone ; Drosophila melanogaster ; Malpighian tubules ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The tissue-specific enzyme urate oxidase is confined exclusively to the Malpighian tubules of Drosophila melanogaster and expressed only in the third-instar larva and the adult. Shortly before pupariation urate oxidase activity declines precipitously and is not detectable 24 hours later. That 20-hydroxyecdysone is the factor that triggers the disappearance of urate oxidase activity in late third-instar larvae is demonstrated using the temperature sensitive mutant ecd1 which at the nonpermissive temperature of 29°C fails to accumulate a sufficient concentration of 20-hydroxyecdysone necessary for puparium formation and thus remains a third-instar larva for 1 to 2 weeks before death. Both the life cycle and the temporal profile of urate oxidase activity in ecd1 larvae at 19°C is identical to that of the wild type. However, at 29°C ecd1 third-instar larvae retain high urate oxidase activity. A precipitous decline in urate oxidase activity is observed when ecd1 larvae at 29°C are fed 20-hydroxyecdysone. These data implicate 20-hydroxyecdysone in the process that controls the rapid decline of urate oxidase activity at the time of puparium formation. In whole homogenates of Malpighian tubules, the urate oxidase polypeptide was identified in SDS-polyacrylamide gels by its Rf with respect to homogeneously pure Drosophila urate oxidase and also by immunoprecipitation with rabbit anti-Drosophila urate oxidase IgG. Throughout development the amount of the urate oxidase polypeptide is correlated with the magnitude of urate oxidase activity.
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  • 64
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    Developmental Genetics 3 (1982), S. 247-253 
    ISSN: 0192-253X
    Keywords: H-Y antigen ; sex determination ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Karyotypically XY individuals of the C57BL/6J-YPOS mouse stock develop as females or hermaphrodites, but never as normal males. The aberrant sexual development results from the interaction of the C57BL/6J genetic background with the M. poschiavinus-derived Y chromosome. XY females from this stock were assayed for H-Y antigen. By the criteria of skin-grafting, the cell-mediated lympholysis test, and the popliteal lymph node assay, these XY females are antigenically indistinguishable from normal C57BL/6 males. Implications for the hypothesis that H-Y antigen induces formation of the mammalian testis are discussed.
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    Developmental Genetics 3 (1982), S. 275-282 
    ISSN: 0192-253X
    Keywords: Drosophila ; sex chromosomes ; gene dosage ; gene expression ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: In Drosophila, the ratio of the number of X chromosomes to sets of other chromosomes initiates a series of events which result in sexual differentiation. In addition, this ratio establishes dosage compensation, a mechanism which equalizes the products of X-linked genes in males and females. The present review discusses possible genetic entities responsible for the interpretation of chromosomal sex and subsequent sex-mediated regulation during development.
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  • 66
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    Developmental Genetics 3 (1982), S. 309-327 
    ISSN: 0192-253X
    Keywords: Drosophila melanogaster ; DNA polymerase ; developmental enzyme profile ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: An assay procedure was developed that allowed the first reproducible measurement of DNA polymerase activity in all developmental stages of Drosophila melanogaster. Evidence is presented that the same enzymatic species is present in extracts of embryos, pupae, and adults of both sexes and that this activity has many properties similar to vertebrate α-polymerases. Polymerase activity per individual is low in embryos and rises steadily through larval instars, reaches a peak in early pupae, declines through the late pupal period, and remains low in newly eclosed adults of both sexes. A dramatic increase is observed in adult females as mature oocytes are formed. This pattern of enzyme activity is completely coincident with changes in DNA levels during development, and suggests that the Drosophila enzyme, like vertebrate α-polymerases, functions in cellular DNA replication. Two mutagen-sensitive mutants, deficient in both replication on undamaged templates and postreplication repair, were found to have normal levels of this α-polymerase activity. Our results suggest that a single enzymatic species of α-polymerase holoenzyme exists in Drosophila and is common to all developmental stages of this organism.
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  • 67
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    Developmental Genetics 4 (1983) 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
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    Developmental Genetics 4 (1983), S. 145-158 
    ISSN: 0192-253X
    Keywords: tetrahymena ; mating type ; differentiation ; macronucleus ; starvation ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Mating type differentiation in Tetrahymena thermophila is known to regularly involve stable hereditary alterations at a single chromosomal locus in the somatic (macro)nucleus. This differentiation is directionally affected by the temperature at which new macronuclei develop after fertilization. We now report large and predictable effects of delayed refeeding of conjugating pairs upon mating type differentiation, particularly among mat-2 homozygotes. The mating types whose frequency is affected the most are IV, VI, and VII, a set different from that most affected by temperature. We interpret our observations to reveal the existence of a second system which can participate in mating type differentiation, with different specificity from the system influenced by temperature under conditions of early refeeding of conjugating pairs. These observations enrich the phenomenology surrounding mating type differentiation in T thermophila and provide additional, easily controllable experimental conditions for the manipulation of mating type frequencies.
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    Developmental Genetics 4 (1983), S. 231-231 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 70
    ISSN: 0192-253X
    Keywords: catalase ; Zea mays ; gene regulation ; temporal genes ; development ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The catalase (H2O2:H2O2 oxidoreductase; E.C.1.11.1.6; CAT) gene-enzyme system in Zea mays L (maize) represents an ideal model for studying the molecular basis of developmental gene regulation in higher eukaryotes. This system comprises a family of structural genes that are highly regulated, both temporally and spatially, during maize development.In maize, there are four distinct forms (isozymes) of catalase that are readily discernible by convetional separation procedures. Three of the catalases have been studied in detail from a genetic and biochemical viewpoint. The catalases CAT-1, CAT-2, and CAT-3 are encoded by the distinct, unlinked genes Cat1, Cat2, and Cat3, respectively. Each of the structural genes is highly regulated both spatially and temporally in its expression. Cat1 is expressed primarily in the endosperm, aleurone, pericarp, and scutellum of developing kernels, and in the root, shoot, and scutellum of very young seedlings. Cat2 is expressed primarily in the scutellum and leaf during postgerminative sporophytic development. Cat3 is expressed, for the most part, in the shoot and pericarp of young seedlings.A number of regulatory variants have been recovered that affect the developmental program of expression of the catalases. Analysis of one variant allowed for the identification of a temporal regulatory gene (Car1) that specifically alters the developmental program of the Cat2 structural gene by acting to regulate the rate of CAT-2 protein synthesis. Cat1 has been mapped on chromosome 1S, 37 map units (m.u.) from the Cat2 structural gene. Another variant line has been isolated which lacks expression of the Cat2 gene in its tissues at all stages of development. Isolated polysomes from this line (A16) were translated in vitro, and the products were immunoprecipitated with CAT-2-specific antibodies. No CAT-2 was detectable in the A16 labeled immunoprecipitates, whereas CAT-2 was readily detected in the normal line, W64A, under similar conditions.The temporal and spatial expression of the Cat structural genes is not only influenced by genetic factors (as above), but is also responsive to exogenously applied environmental signals: light, hormones, and temperature. The mechanisms by which such signals specifically affect CAT-2 expression will be discussed.
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  • 71
    ISSN: 0192-253X
    Keywords: genetic variation ; molecular evolution ; natural selection ; DNA polymorphism ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The evidence for genetic variation can be traced to Mendel's experiments: The discovery of the laws of heredity was made possible by the expression of segregating alleles. Since that time, the study of genetic variation in natural populations has been characterized by a gradual discovery of ever-increasing amounts of genetic variation. In the early decades of this century geneticists thought that an individual is homozygous at most gene loci and that individuals of the same species are genetically almost identical. Recent discoveries suggest that, at least in outcrossing organisms, the DNA sequences inherited one from each parent are likely to be different for nearly every gene locus in every individual; ie, that every individual may be heterozygous at most, if not all, gene loci. But the efforts to obtain precise estimates of genetic variation have been thwarted for various reasons.
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    Developmental Genetics 4 (1983), S. 451-451 
    ISSN: 0192-253X
    Keywords: Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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