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Blue light-induced transcription of plastid-encoded psbD gene is mediated by a nuclear-encoded transcription initiation factor, AtSig5

机译:质体编码的psbD基因的蓝光诱导转录由核编码的转录起始因子AtSig5介导。

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摘要

Light is one of the most important environmental factors regulating expression of photosynthesis genes. The plastid psbD gene encoding the photosystem II reaction center protein D2 is under the control of a unique blue light responsive promoter (BLRP) that is transcribed by a bacterial-type plastid RNA polymerase (PEP). Promoter recognition of PEP is mediated by one of the six nuclear-encoded σ factors in Arabidopsis. The replacement of the plastid σ factor associated with PEP may be the major mechanism for switching of plastid transcription pattern in response to environmental and developmental signals. This study demonstrates that AtSig5 is a unique σ factor that is essential for psbD BLRP activity. A T-DNA insertional mutant with reduced AtSIG5 expression resulted in loss of primary transcripts from the psbD BLRP. Furthermore, transient overexpression of AtSig5 in dark-adapted protoplasts specifically elevated psbD and psbA transcription activities. On the other hand, overproduction of AtSig2 enhanced the transcription of psbA gene and trnE operon, but not psbD transcription. The AtSIG5 gene is phylogenetically distinct from other plastid σ factors, and its expression is induced exclusively by blue light. We propose that AtSig5 acts as a mediator of blue light signaling that specifically activates the psbD BLRP in response to blue light in Arabidopsis.
机译:光是调节光合作用基因表达的最重要的环境因素之一。编码光系统II反应中心蛋白D2的质体psbD基因在独特的蓝光响应启动子(BLRP)的控制下,该启动子由细菌型质体RNA聚合酶(PEP)转录。对PEP的启动子识别是由拟南芥中六个核编码的σ因子之一介导的。与PEP相关的质体σ因子的替换可能是响应环境和发育信号而转换质体转录模式的主要机制。这项研究表明,AtSig5是一个独特的σ因子,对于psbD BLRP活性至关重要。 AtSIG5表达降低的T-DNA插入突变体导致psbD BLRP的初级转录本丢失。此外,在黑暗适应的原生质体中,AtSig5的瞬时过表达特异性提高了psbD和psbA转录活性。另一方面,AtSig2的过量生产增强了psbA基因和trnE操纵子的转录,但不增强psbD转录。 AtSIG5基因在系统发育上与其他质体σ因子不同,其表达仅由蓝光诱导。我们建议AtSig5充当蓝光信号的介体,该信号可专门响应拟南芥中的蓝光而激活psbD BLRP。

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