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Plastid Transcription in Higher Plants Yoshinori Toyoshima and Yayoi Onda

机译:高等植物丰义义典和恩田弥生的质体转录

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The plastid genome is transcribed by nucleus-encoded (NEP) and plastid encoded (PEP) RNA polymerases. NEP transcribes housekeeping genes as well as genes coding for PEP core sub-units and its activity is replaced by PEP in chloroplasts resulting in differential expression of genes in a developmental context. PEP is a prokaryotic-type enzyme in which nuclear-encoded a factors function as promoter recognition subunit. A phylogenetic analysis for a factors identified so far in plants shows that plant sigma factors are members of bacterial sigma~(70) family and divided into six groups, Sigl through Sig6, which are integrated into four clusters consisting of Sigl and Sig4, Sig2 and Sig3, Sig5 and Sig6. All plastid sigma- factors recognize bacterial sigma~(70)-type promoters, but they differ in promoter preference and the tissue-, developmental stage-and environmental-dependent expression. Sig5 is distinct from the other cr factors in its structure, function, and expression in response to light and stress. A promoter of the psbD operon, psbD blue light responsive promoter (psbDBLRP) is a typical example that is under the control of a combination of various signals arising in the nucleus and plastids in response to the tissue specific and developmental stage- and environment-dependent cues. psbDBLRP is recognized only by Sig5, which is expressed by a cryptochrome-mediated blue light signal and signals responding to stress conditions. The activity of psbDBLRP is also under the control of circadian clock.Furthermore, it may be regulated by redox signals generated by photosynthetic electron transport in the chloroplast presumably through the change of the binding affinity of a nuclear encoded transcription factor for the enhancer element located upstreamof the core promoter region of the psbD operon.
机译:质体基因组通过核编码(NEP)和质体编码(PEP)RNA聚合酶转录。 NEP转录管家基因以及编码PEP核心亚基的基因,其活性被叶绿体中的PEP取代,从而导致基因在发育环境中的差异表达。 PEP是一种原核生物型酶,其中的核编码因子起启动子识别亚基的作用。对迄今为止在植物中发现的因素进行的系统发育分析表明,植物sigma因子是细菌sigma〜(70)家族的成员,分为从Sigl至Sig6的六类,它们被整合为由Sigl和Sig4,Sig2和Sig4组成的四个簇。 Sig3,Sig5和Sig6。所有质体sigma-因子均识别细菌sigma〜(70)型启动子,但它们在启动子偏好以及组织,发育阶段和环境依赖性表达方面有所不同。 Sig5在响应光和压力的结构,功能和表达方面与其他cr因子不同。 psbD操纵子的启动子,psbD蓝光响应启动子(psbDBLRP)是一个典型的例子,它受组织和发育阶段及环境依赖性的细胞核和质体中各种信号的组合控制提示。 psbDBLRP仅由Sig5识别,Sig5由隐色介导的蓝光信号和对压力条件作出响应的信号表示。 psbDBLRP的活性也受昼夜节律的控制。此外,它可能受叶绿体中光合作用电子传输产生的氧化还原信号的调节,大概是通过改变核编码转录因子对位于上游的增强子的结合亲和力来实现的。 psbD操纵子的核心启动子区域。

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