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一个五肽重复序列蛋白通过切割线粒体orf312 RNA恢复了田ukan型细胞质雄性不育水稻的育性。

A Pentatricopeptide Repeat Protein Restores Fertility in Tadukan-Type Cytoplasmic Male Sterile Rice via the Cleavage of the Mitochondrial orf312 RNA.

作者信息

Takatsuka Ayumu, Iwai Yuko, Mireau Hakim, Kazama Tomohiko, Ichida Hiroyuki, Abe Tomoko, Igarashi Keisuke, Toriyama Kinya

机构信息

Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan.

Institute Jean-Pierre Bourgin for Plant Sciences (IJPB), Université Paris-Saclay, INRAE, AgroParisTech, Versailles, France.

出版信息

Physiol Plant. 2025 May-Jun;177(3):e70308. doi: 10.1111/ppl.70308.

Abstract

Cytoplasmic male sterility (CMS) is associated with the inhibition of pollen and/or anther development regulated by a CMS-causing gene in the mitochondrial genome; it is a useful trait for preventing self-pollination and producing F hybrids, which can boost crop yields. Pollen and/or anther development can be recovered by the action of the RESTORER OF FERTILITY (Rf) gene, a nuclear-encoded gene. Most reported Rf genes encode pentatricopeptide repeat (PPR) proteins, which bind to RNA and promote RNA processing of the respective CMS-causing gene. In this study, we report the map-based cloning of the Rf gene (Rfta) for Tadukan-type CMS (TA-CMS) in rice (Oryza sativa L.), with anther dehiscence and seed setting inhibited by the mitochondrial gene orf312. The Rfta locus was delimited to a region comprising 10 PPR genes forming a cluster on chromosome 10. The complementation test revealed that the introduction of a PPR gene, PPR796, into the TA-CMS line resulted in the recovery of the anther dehiscence and seed setting. RNA-gel blot analysis and the determination of 3' ends of the orf312 RNA confirmed the PPR796-mediated cleavage of the orf312 RNA in the transgenic TA-CMS line. Furthermore, RNA gel electrophoretic mobility shift assays revealed that the recombinant PPR796 protein bound to the 3' side of the orf312 RNA in vitro. We concluded that RFta/PPR796 binds to orf312 RNA and promotes RNA cleavage to restore fertility in TA-CMS.

摘要

细胞质雄性不育(CMS)与线粒体基因组中导致CMS的基因调控的花粉和/或花药发育抑制有关;它是防止自花授粉和生产F杂种的有用性状,可提高作物产量。花粉和/或花药发育可通过育性恢复基因(Rf)的作用得以恢复,Rf是一个核编码基因。大多数已报道的Rf基因编码五肽重复序列(PPR)蛋白,该蛋白与RNA结合并促进相应的导致CMS的基因的RNA加工。在本研究中,我们报道了水稻(Oryza sativa L.)中田ukan型CMS(TA-CMS)的Rf基因(Rfta)的图位克隆,其花药开裂和结实受到线粒体基因orf312的抑制。Rfta基因座被定位到10号染色体上包含10个PPR基因的一个簇的区域。互补试验表明,将PPR基因PPR796导入TA-CMS系可恢复花药开裂和结实。RNA凝胶印迹分析和orf312 RNA 3'端的测定证实了转基因TA-CMS系中PPR796介导的orf312 RNA的切割。此外,RNA凝胶电泳迁移率变动分析表明,重组PPR796蛋白在体外与orf312 RNA的3'端结合。我们得出结论,RFta/PPR796与orf312 RNA结合并促进RNA切割,以恢复TA-CMS的育性。

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