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两种衣藻 OPR 蛋白稳定编码光系统 II 和细胞色素 b6 f 的小亚基的叶绿体 mRNA。

Two Chlamydomonas OPR proteins stabilize chloroplast mRNAs encoding small subunits of photosystem II and cytochrome b6 f.

机构信息

UMR 7141, Centre National de la Recherche Scientifique/Université Pierre et Marie Curie, Institut de Biologie Physico-Chimique, Paris, 75005, France.

Biozentrum Ludwig-Maximilians-Universität München, D-82152, Planegg-Martinsried, Germany.

出版信息

Plant J. 2015 Jun;82(5):861-73. doi: 10.1111/tpj.12858.

DOI:10.1111/tpj.12858
PMID:25898982
Abstract

In plants and algae, chloroplast gene expression is controlled by nucleus-encoded proteins that bind to mRNAs in a specific manner, stabilizing mRNAs or promoting their splicing, editing, or translation. Here, we present the characterization of two mRNA stabilization factors of the green alga Chlamydomonas reinhardtii, which both belong to the OctotricoPeptide Repeat (OPR) family. MCG1 is necessary to stabilize the petG mRNA, encoding a small subunit of the cytochrome b6 f complex, while MBI1 stabilizes the psbI mRNA, coding for a small subunit of photosystem II. In the mcg1 mutant, the small RNA footprint corresponding to the 5'-end of the petG transcript is reduced in abundance. In both cases, the absence of the small subunit perturbs assembly of the cognate complex. Whereas PetG is essential for formation of a functional cytochrome b6 f dimer, PsbI appears partly dispensable as a low level of PSII activity can still be measured in its absence. Thus, nuclear control of chloroplast gene expression is not only exerted on the major core subunits of the complexes, but also on small subunits with a single transmembrane helix. While OPR proteins have thus far been involved in translation or trans-splicing of plastid mRNAs, our results expand the potential roles of this repeat family to their stabilization.

摘要

在植物和藻类中,叶绿体基因表达受核编码蛋白控制,这些蛋白以特定方式结合 mRNA,稳定 mRNA 或促进其剪接、编辑或翻译。在这里,我们描述了绿藻衣藻中两种 mRNA 稳定因子的特征,它们都属于八肽重复(OPR)家族。MCG1 对于稳定编码细胞色素 b6 f 复合物小亚基的 petG mRNA 是必需的,而 MBI1 稳定编码光系统 II 小亚基的 psbI mRNA。在 mcg1 突变体中,与 petG 转录物 5'-端对应的小 RNA 足迹的丰度减少。在这两种情况下,小亚基的缺失都会扰乱同源复合物的组装。虽然 PetG 对于功能性细胞色素 b6 f 二聚体的形成是必需的,但 PsbI 似乎部分是可有可无的,因为在其缺失的情况下仍可以测量到低水平的 PSII 活性。因此,核对叶绿体基因表达的控制不仅施加于复合物的主要核心亚基上,还施加于具有单个跨膜螺旋的小亚基上。虽然 OPR 蛋白迄今已参与质体 mRNA 的翻译或转剪接,但我们的结果扩展了该重复家族的潜在作用,使其稳定化。

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