Takatsuka Ayumu, Iwai Yuko, Mireau Hakim, Kazama Tomohiko, Ichida Hiroyuki, Abe Tomoko, Igarashi Keisuke, Toriyama Kinya
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.
Physiol Plant. 2025 May-Jun;177(3):e70308. doi: 10.1111/ppl.70308.
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.
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。