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  • http://hdl.handle.net/10402/era.29466
  • Redox-regulated RNA helicase expression
  • Kujat, S. L.
    Owttrim, G. W.
  • Mustard Sinapsis-Alba
    PSBA Messenger-RNA
    Protein-Phosphorylation
    Gene-Expression
    Cyanobacterium Synechocystis-6803
    Plastoquinone Pool
    Light
    Chloroplast
    Transcription
    Photosynthesis
  • Journal Article (Published)
  • English
  • Adobe PDF
  • 437216 bytes
  • In photosynthetic organisms it is becoming increasingly evident that light-driven shifts in redox potential act as a sensor that initiates alterations in gene expression at both the level of transcription and translation. This report provides evidence that the expression of a cyanobacterial RNA helicase gene, crhR, is controlled at the level of transcription and mRNA stability by a complex series of interacting mechanisms that are redox regulated. Transcript accumulation correlates with reduction of the electron transport chain between QA in photosystem II and QO in cyt b6f, when Synechocystis sp. strain PCC 6803 is cultured photoautotrophically or photomixotrophically and subjected to darkness and/or electron transport inhibitors or illumination that preferentially excites photosystem II. crhR mRNA stability is also regulated by a redox responsive mechanism, which differs from that affecting accumulation and does not involve signaling initiated by photoreceptors. The data are most consistent with plastoquinol/cyt b6 f interaction as the sensor initiating a signal transduction cascade resulting in accumulation of the crhR transcript. Functionally, CrhR RNA unwinding could act as a linker between redox regulated transcription and translation. The potential for translational regulation of redox-induced gene expression through RNA helicase-catalyzed modulation of RNA secondary structure is discussed.
  • Kujat, S.L. & Owttrim, G.W. (2000). Redox-regulated RNA helicase expression. Plant Physiology, 124(2), 703-713. doi: 10.1104/pp.124.2.703.