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核编码的σ因子SIG4直接激活单细胞红藻梅氏嗜热栖热菌中叶绿体psbA和ycf17基因的转录。

The nuclear-encoded sigma factor SIG4 directly activates transcription of chloroplast psbA and ycf17 genes in the unicellular red alga Cyanidioschyzon merolae.

作者信息

Fujii Gaku, Imamura Sousuke, Era Atsuko, Miyagishima Shin-ya, Hanaoka Mitsumasa, Tanaka Kan

机构信息

Chemical Resources Laboratory, Tokyo Institute of Technology, 4259-R1-29 Nagatsuta, Midori-ku, Yokohama 226-8503, Japan.

Chemical Resources Laboratory, Tokyo Institute of Technology, 4259-R1-29 Nagatsuta, Midori-ku, Yokohama 226-8503, Japan Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST), Saitama 332-0012, Japan.

出版信息

FEMS Microbiol Lett. 2015 May;362(10). doi: 10.1093/femsle/fnv063. Epub 2015 Apr 15.

Abstract

The plant organelle chloroplast originated from the endosymbiosis of a cyanobacterial-like photosynthetic bacterium, and still retains its own genome derived from this ancestor. We have been focusing on a unicellular red alga, Cyanidioschyzon merolae, as a model photosynthetic eukaryote. In this study, we analyzed the transcriptional specificity of SIG4, which is one of four nuclear-encoded chloroplast RNA polymerase sigma factors in this alga. Accumulation of the SIG4 protein was observed in response to nitrogen depletion or high light conditions. By comparing the chloroplast transcriptomes under nitrogen depletion and SIG4-overexpressing conditions, we identified several candidate genes as SIG4 targets. Together with the results of chromatin immunoprecipitation analysis, the promoters of the psbA (encoding the D1 protein of the photosystem II reaction center) and ycf17 (encoding a protein of the early light-inducible protein family) genes were shown to be direct activation targets. The phycobilisome (PBS) CpcB protein was decreased by SIG4 overexpression, which suggests the negative involvement of SIG4 in PBS accumulation.

摘要

植物细胞器叶绿体起源于一种类似蓝细菌的光合细菌的内共生作用,并且仍然保留着源自该祖先的自身基因组。我们一直专注于单细胞红藻——嗜热栖热放线菌(Cyanidioschyzon merolae),将其作为光合真核生物的模型。在本研究中,我们分析了SIG4的转录特异性,SIG4是该藻类中四个核编码叶绿体RNA聚合酶sigma因子之一。在氮缺乏或高光条件下观察到SIG4蛋白的积累。通过比较氮缺乏和SIG4过表达条件下的叶绿体转录组,我们鉴定出几个候选基因作为SIG4的靶标。结合染色质免疫沉淀分析的结果,psbA(编码光系统II反应中心的D1蛋白)和ycf17(编码早期光诱导蛋白家族的一种蛋白质)基因的启动子被证明是直接激活靶标。藻胆体(PBS)CpcB蛋白通过SIG4过表达而减少,这表明SIG4对PBS积累有负面作用。

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