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五肽重复蛋白EMB2654对叶绿体小核糖体亚基转录本的反式剪接至关重要。

The Pentatricopeptide Repeat Protein EMB2654 Is Essential for Trans-Splicing of a Chloroplast Small Ribosomal Subunit Transcript.

作者信息

Aryamanesh Nader, Ruwe Hannes, Sanglard Lilian Vincis Pereira, Eshraghi Leila, Bussell John D, Howell Katharine A, Small Ian, des Francs-Small Catherine Colas

机构信息

Australian Research Council Centre of Excellence in Plant Energy Biology, University of Western Australia, Crawley 6009 Western Australia, Australia (N.A., H.R., L.V.P.S., L.E., J.D.B., K.A.H., I.S., C.C.d.F.-S.); and.

Institute of Biology, Humboldt-University of Berlin, 10115 Berlin, Germany (H.R.).

出版信息

Plant Physiol. 2017 Feb;173(2):1164-1176. doi: 10.1104/pp.16.01840. Epub 2016 Dec 23.

Abstract

We report the partial complementation and subsequent comparative molecular analysis of two nonviable mutants impaired in chloroplast translation, one (emb2394) lacking the RPL6 protein, and the other (emb2654) carrying a mutation in a gene encoding a P-class pentatricopeptide repeat protein. We show that EMB2654 is required for the trans-splicing of the plastid rps12 transcript and that therefore the emb2654 mutant lacks Rps12 protein and fails to assemble the small subunit of the plastid ribosome, explaining the loss of plastid translation and consequent embryo-lethal phenotype. Predictions of the EMB2654 binding site match a small RNA "footprint" located on the 5' half of the trans-spliced intron that is almost absent in the partially complemented mutant. EMB2654 binds sequence specifically to this target sequence in vitro. Altered patterns in nuclease-protected small RNA fragments in emb2654 show that EMB2654 binding must be an early step in, or prior to, the formation of a large protein-RNA complex covering the free ends of the two rps12 intron halves.

摘要

我们报道了两个叶绿体翻译受损的无活力突变体的部分互补及后续的比较分子分析,其中一个突变体(emb2394)缺乏RPL6蛋白,另一个突变体(emb2654)在编码P类五肽重复蛋白的基因中发生了突变。我们发现EMB2654是质体rps12转录本反式剪接所必需的,因此emb2654突变体缺乏Rps12蛋白,无法组装质体核糖体的小亚基,这就解释了质体翻译的丧失以及随之而来的胚胎致死表型。EMB2654结合位点的预测结果与位于反式剪接内含子5'端一半的一个小RNA“足迹”相匹配,而在部分互补突变体中该“足迹”几乎不存在。EMB2654在体外能序列特异性地结合该靶序列。emb2654中核酸酶保护的小RNA片段模式的改变表明,EMB2654的结合必定是形成覆盖两个rps12内含子半体自由末端的大型蛋白质-RNA复合物过程中的早期步骤,或者是在此之前的步骤。

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