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蓝光诱导的质体编码的psbD基因转录由一个核编码的转录起始因子AtSig5介导。

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

作者信息

Tsunoyama Yuichi, Ishizaki Yoko, Morikawa Kazuya, Kobori Maki, Nakahira Yoichi, Takeba Go, Toyoshima Yoshinori, Shiina Takashi

机构信息

Radioisotope Research Center, Kyoto University, Kitashirakawa-oiwake-cho, Sakyo-ku Kyoto 606-8502, Japan.

出版信息

Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):3304-9. doi: 10.1073/pnas.0308362101. Epub 2004 Feb 19.

Abstract

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 sigma factors in Arabidopsis. The replacement of the plastid sigma 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 sigma 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 sigma 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.

摘要

光是调节光合作用基因表达的最重要环境因素之一。编码光系统II反应中心蛋白D2的质体psbD基因受一个独特的蓝光响应启动子(BLRP)控制,该启动子由细菌型质体RNA聚合酶(PEP)转录。PEP对启动子的识别由拟南芥中六个核编码的sigma因子之一介导。与PEP相关的质体sigma因子的替换可能是响应环境和发育信号而切换质体转录模式的主要机制。本研究表明,AtSig5是一种独特的sigma因子,对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的初级转录本缺失。此外,在暗适应的原生质体中瞬时过表达AtSig5可特异性提高psbD和psbA的转录活性。另一方面,AtSig2的过量产生增强了psbA基因和trnE操纵子的转录,但不增强psbD的转录。AtSIG5基因在系统发育上与其他质体sigma因子不同,其表达仅由蓝光诱导。我们提出,AtSig5作为蓝光信号的介导因子,在拟南芥中响应蓝光特异性激活psbD BLRP。

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