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  • Articles  (2)
  • Ribulose 1,5-bisphosphate carboxylase/oxygenase  (2)
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  • 1
    ISSN: 1432-2048
    Keywords: Blue-light photoreceptor ; Gene expression (rbcS) ; Phaseolus ; Photoregulation ; Ribulose 1,5-bisphosphate carboxylase/oxygenase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The level of transcripts of genes encoding the small subunit of ribulose 1,5-bisphosphate carboxylase/oxygenase (rbcS genes) in the primary leaves of Phaseolus vulgaris L. increases substantially when plants grown in a low fluence rate of white light (15 μmol m−2 s−1; 400–700 nm) are transferred to a tenfold higher fluence rate of identical spectral quality. To investigate which photoreceptor acts as the fluence-rate detector, plants grown for 16 d in low white light were transferred to blue-enriched or red light environments of various fluence rates. The results indicate that the fluence-rate-dependent increase in rbcS expression is mediated specifically by blue light. Red light of the same fluence rate, which was found to be equally effective in driving photosynthesis, had much less effect on expression, indicating that light absorbed by the photosynthetic pigments does not mediate the response. Moreover, there is no correlation of the transcript levels with either the cycling rate or photoequilibrium of the phytochrome system. Run-on assays with isolated nuclei indicate that blue light substantially increases the rate of rbcS transcription. Experiments with gene-specific probes show that individual members of the P. vulgaris rbcS gene family exhibit the fluence-rate-dependent, blue-light-mediated increase in expression.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Ribulose 1,5-bisphosphate carboxylase/oxygenase ; rbcS genes ; Leaf development ; Photoregulation ; Phaseolus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The rbcS1, 2 and 3 genes of Phaseolus vulgaris are identical in coding sequence and we have studied their expression using gene-specific probes derived from their 3′ non-coding regions. The genes differ in their relative levels of expression but show only minor qualitative differences in their regulation. Transcripts of the three genes are undetectable in primary leaves in the imbibed seed, accumulate early in leaf expansion reaching a maximum 7–10 d after sowing and decrease to low levels by the time expansion is complete. Both dark-grown and light-grown primary leaves exhibit this ontogenetic pattern of expression, although the light-grown leaves have two to three times more rbcS transcripts. Light can over-ride the ontogenetic control of rbcS expression; for example, when 7-d-old dark-grown primary leaves are illuminated there is a 6- to 12-fold increase in the transcript levels of the rbcS genes. Transfer of illuminated leaves to darkness results in the loss of transcripts of all three genes, but rbcS2 transcripts persist in the dark-adapted leaves. Possible physiological mechanisms of the ontogenetic regulation of expression are discussed.
    Type of Medium: Electronic Resource
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