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  • ACC synthase gene  (1)
  • Inverted repeat  (1)
  • Springer  (2)
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  • Springer  (2)
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  • 1
    ISSN: 1432-0983
    Keywords: Key words Intermolecular recombination ; Inverted repeat ; Oryza sativa ; Plastid DNA (PtDNA)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We have determined the nucleotide sequences around the junction points of oligomeric-deleted ptDNAs possessing a head-to-head or tail-to-tail configuration from long-term cultured cell lines and albino plants. It was shown that DNA rearrangement occurred by direct fusion of deleted ptDNAs in an inverted orientation, which was linked by an asymmetrical sequence of 254–698 bp derived from either of the ptDNAs joined. It is notable that inverted repeats of 7–14 bp flank the asymmetrical sequences at each of the junction points. These features of the DNA sequence around the junction points are commonly observed in oligomeric ptDNA with a large-scale deletion regardless of the cell lines employed. It is suggested that the short inverted repeats are involved in the intermolecular recombination of ptDNA.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2242
    Keywords: Key words Malus×domestica Borkh. ; Ethylene ; Ripening ; ACC synthase gene ; Storage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  An allele of the apple ripening-specific 1- aminocyclopropane-1-carboxylate (ACC) synthase gene (Md-ACS1–1) has a 5′-flanking region possessing an inserted retroposon-like sequence. Apple species can be classified into three groups that are heterozygous or homozygous for the ACS1–1 and ACS1–2 alleles. We measured the internal ethylene concentration (IEC) in climacteric fruit of 35 apple cultivars with respect to genotype. Eleven ACS1–2 homozygous cultivars exhibited much lower IECs than cultivars homozygous or heterozygous for ACS1–1. Furthermore, F1 ACS1–2 homozygous progeny derived from crosses between heterozygous cultivars had fruit with a very low IEC. These results are in accord with previous data indicating the absence of transcription from ACS1–2 in a heterozygous cultivar. Since the low level of ACS1 mRNA in climacteric fruit was observed in several ACS1–2 homozygous cultivars, we conclude that the low level of ethylene production in some cultivars is caused by the mutated allele of ACS1, which is the main gene responsible for ethylene production during ripening.
    Type of Medium: Electronic Resource
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