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水稻五重基序重复蛋白 RF5 通过与富含甘氨酸的蛋白 GRP162 形成复合物,恢复红莲胞质雄性不育系的育性。

The rice pentatricopeptide repeat protein RF5 restores fertility in Hong-Lian cytoplasmic male-sterile lines via a complex with the glycine-rich protein GRP162.

机构信息

Key Laboratory of the Ministry of Education for Plant Developmental Biology, College of Life Sciences, Wuhan University, Wuhan 430072, China.

出版信息

Plant Cell. 2012 Jan;24(1):109-22. doi: 10.1105/tpc.111.093211. Epub 2012 Jan 13.

Abstract

The cytoplasmic male sterility (CMS) phenotype in plants can be reversed by the action of nuclear-encoded fertility restorer (Rf) genes. The molecular mechanism involved in Rf gene-mediated processing of CMS-associated transcripts is unclear, as are the identities of other proteins that may be involved in the CMS-Rf interaction. In this study, we cloned the restorer gene Rf5 for Hong-Lian CMS in rice and studied its fertility restoration mechanism with respect to the processing of the CMS-associated transcript atp6-orfH79. RF5, a pentatricopeptide repeat (PPR) protein, was unable to bind to this CMS-associated transcript; however, a partner protein of RF5 (GRP162, a Gly-rich protein encoding 162 amino acids) was identified to bind to atp6-orfH79. GRP162 was found to physically interact with RF5 and to bind to atp6-orfH79 via an RNA recognition motif. Furthermore, we found that RF5 and GRP162 are both components of a restoration of fertility complex (RFC) that is 400 to 500 kD in size and can cleave CMS-associated transcripts in vitro. Evidence that a PPR protein interacts directly with a Gly-rich protein to form a subunit of the RFC provides a new perspective on the molecular mechanisms underlying fertility restoration.

摘要

植物细胞质雄性不育(CMS)表型可以被核编码的育性恢复(Rf)基因所逆转。Rf 基因介导 CMS 相关转录本加工的分子机制尚不清楚,可能参与 CMS-Rf 相互作用的其他蛋白质的身份也不清楚。在这项研究中,我们克隆了水稻红莲 CMS 的恢复基因 Rf5,并研究了其育性恢复机制,涉及 CMS 相关转录本 atp6-orfH79 的加工。RF5 是一个五肽重复(PPR)蛋白,无法与这个 CMS 相关转录本结合;然而,RF5 的一个伴侣蛋白(GRP162,一个编码 162 个氨基酸的富含甘氨酸的蛋白)被鉴定为与 atp6-orfH79 结合。GRP162 被发现与 RF5 物理相互作用,并通过 RNA 识别基序与 atp6-orfH79 结合。此外,我们发现 RF5 和 GRP162 都是大小为 400 到 500 kD 的育性恢复复合体(RFC)的组成部分,并且可以在体外切割 CMS 相关转录本。直接与富含甘氨酸的蛋白质相互作用的 PPR 蛋白形成 RFC 的亚基的证据,为育性恢复的分子机制提供了一个新的视角。

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