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The RNA-binding proteins CSP41a and CSP41b may regulate transcription and translation of chloroplast-encoded RNAs in Arabidopsis

机译:RNA结合蛋白CSP41a和CSP41b可能调节拟南芥中叶绿体编码的RNA的转录和翻译

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The chloroplast protein CSP41a both binds and cleaves RNA, particularly in stem-loops, and has been found associated with ribosomes. A related protein, CSP41b, co-purifies with CSP41a, ribosomes, and the plastid-encoded RNA polymerase. Here we show that Arabidopsis CSP41a and CSP41b interact in vivo, and that a csp41b null mutant becomes depleted of CSP41a in mature leaves, correlating with a pale green phenotype and reduced accumulation of the ATP synthase and cytochrome b (6) /f complexes. RNA gel blot analyses revealed up to four-fold decreases in accumulation for some chloroplast RNAs, which run-on experiments suggested could tentatively be ascribed to decreased transcription. Depletion of both CSP41a and CSP41b triggered a promoter switch whereby atpBE became predominately transcribed from its nucleus-encoded polymerase promoter as opposed to its plastid-encoded polymerase promoter. Together with published proteomic data, this suggests that CSP41a and/or CSP41b enhances transcription by the plastid-encoded polymerase. Gradient analysis of rRNAs in the mutant suggest a defect in polysome assembly or stability, suggesting that CSP41a and/or CSP41b, which are not present in polysomal fractions, stabilize ribosome assembly intermediates. Although psbA and rbcL mRNAs are normally polysome-associated in the mutant, petD-containing RNAs have diminished association, perhaps accounting for reduced accumulation of its respective multimeric complex. In conclusion, our data suggest that CSP41a and CSP41b stimulate both transcription and translation in the chloroplast.
机译:叶绿体蛋白CSP41a既可以结合也可以切割RNA,特别是在茎环中,并且已经与核糖体相关。相关蛋白CSP41b与CSP41a,核糖体和质体编码的RNA聚合酶共同纯化。在这里,我们显示拟南芥CSP41a和CSP41b在体内相互作用,并且csp41b无效突变体在成熟叶片中耗尽了CSP41a,与淡绿色表型和ATP合酶和细胞色素b(6)/ f复合物的积累减少相关。 RNA凝胶印迹分析显示,某些叶绿体RNA的积累最多可减少四倍,该连续实验表明,暂定归因于转录降低。 CSP41a和CSP41b的耗尽触发了启动子转换,由此atpBE从其核编码的聚合酶启动子开始转录,而不是其质体编码的聚合酶启动子转录。连同已发表的蛋白质组学数据,这表明CSP41a和/或CSP41b通过质体编码的聚合酶增强转录。突变体中rRNA的梯度分析表明多核糖体组装或稳定性方面存在缺陷,这表明多聚体级分中不存在的CSP41a和/或CSP41b稳定了核糖体组装中间体。尽管psbA和rbcL mRNA在突变体中通常与多核糖体相关,但含petD的RNA却减少了相关性,这也许可以解释其各自的多聚体复合物的积累减少。总之,我们的数据表明CSP41a和CSP41b刺激叶绿体中的转录和翻译。

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