Ming Li, Lianjie Feng, Huanxia Ye, Meiyu Li, Jing Jin, Li-Zhen Tao, Huili Liu
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Further analysis using the BiFC assay revealed that the gef10-W260S mutation disrupted the recruitment of rice histidine phosphotransfer proteins (OsAHP1/2) to the plasma membrane (PM), thereby promoting cytokinin signaling. This effect was corroborated by a dark-induced leaf senescence assay, which revealed an increased cytokinin response in the gef10-W260S ectopic expression lines, whereas the overexpression lines presented a suppressed cytokinin response. Moreover, we revealed that the enhanced panicle development in the gef10-W260S lines was attributable to the upregulated expression of several type-B response regulators (RRs) that are crucial for panicle development. Collectively, these findings revealed the negative regulatory function of OsRopGEF10 in the development of the shoot apical meristem (SAM) via interference with cytokinin signaling. Our study highlights the promising role of OsRopGEF10 as a potential target for regulating SAM and panicle development in rice, revealing a valuable breeding strategy for increasing crop yield.</p>","PeriodicalId":21408,"journal":{"name":"Rice","volume":"17 1","pages":"57"},"PeriodicalIF":4.8000,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11369127/pdf/","citationCount":"0","resultStr":"{\"title\":\"OsRopGEF10 Attenuates Cytokinin Signaling to Regulate Panicle Development and Grain Yield in Rice.\",\"authors\":\"Ming Li, Lianjie Feng, Huanxia Ye, Meiyu Li, Jing Jin, Li-Zhen Tao, Huili Liu\",\"doi\":\"10.1186/s12284-024-00737-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cytokinins, which play crucial roles in shoot development, substantially affect grain yield. In rice, the OsRopGEF10-OsRAC3 module is associated with cytokinin signaling and crown root development. However, the effects of RopGEF-mediated cytokinin signaling on rice shoot development and grain yield remain unclear. In this study, we investigated the role of OsRopGEF10 in SAM development and the underlying mechanism. We showed that overexpression of OsRopGEF10 inhibited SAM and panicle development, leading to decreased grain yield. Intriguingly, the overexpression of a specific amino acid mutant of OsRopGEF10, designated gef10-W260S, was found to promote panicle development and grain yield. Further analysis using the BiFC assay revealed that the gef10-W260S mutation disrupted the recruitment of rice histidine phosphotransfer proteins (OsAHP1/2) to the plasma membrane (PM), thereby promoting cytokinin signaling. This effect was corroborated by a dark-induced leaf senescence assay, which revealed an increased cytokinin response in the gef10-W260S ectopic expression lines, whereas the overexpression lines presented a suppressed cytokinin response. Moreover, we revealed that the enhanced panicle development in the gef10-W260S lines was attributable to the upregulated expression of several type-B response regulators (RRs) that are crucial for panicle development. Collectively, these findings revealed the negative regulatory function of OsRopGEF10 in the development of the shoot apical meristem (SAM) via interference with cytokinin signaling. 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引用次数: 0
摘要
细胞分裂素在芽的发育过程中起着至关重要的作用,对谷物产量有很大影响。在水稻中,OsRopGEF10-OsRAC3 模块与细胞分裂素信号转导和冠根发育有关。然而,RopGEF 介导的细胞分裂素信号转导对水稻芽发育和谷物产量的影响仍不清楚。在本研究中,我们研究了 OsRopGEF10 在 SAM 发育中的作用及其内在机制。结果表明,过表达 OsRopGEF10 会抑制 SAM 和圆锥花序的发育,导致谷物产量下降。耐人寻味的是,过表达 OsRopGEF10 的一个特定氨基酸突变体(gef10-W260S)可促进圆锥花序的发育和谷粒产量的提高。利用 BiFC 分析法进行的进一步分析表明,gef10-W260S 突变扰乱了水稻组氨酸磷酸转移蛋白(OsAHP1/2)向质膜(PM)的募集,从而促进了细胞分裂素信号转导。黑暗诱导的叶片衰老试验证实了这一效应,该试验显示gef10-W260S异位表达株的细胞分裂素反应增强,而过表达株的细胞分裂素反应受到抑制。此外,我们还发现gef10-W260S异位表达株的圆锥花序发育增强是由于对圆锥花序发育至关重要的几种B型反应调节因子(RRs)的表达上调所致。总之,这些发现揭示了 OsRopGEF10 通过干扰细胞分裂素信号在嫩枝顶端分生组织(SAM)发育过程中的负调控功能。我们的研究凸显了 OsRopGEF10 作为调控水稻 SAM 和圆锥花序发育的潜在靶标的重要作用,为提高作物产量提供了有价值的育种策略。
OsRopGEF10 Attenuates Cytokinin Signaling to Regulate Panicle Development and Grain Yield in Rice.
Cytokinins, which play crucial roles in shoot development, substantially affect grain yield. In rice, the OsRopGEF10-OsRAC3 module is associated with cytokinin signaling and crown root development. However, the effects of RopGEF-mediated cytokinin signaling on rice shoot development and grain yield remain unclear. In this study, we investigated the role of OsRopGEF10 in SAM development and the underlying mechanism. We showed that overexpression of OsRopGEF10 inhibited SAM and panicle development, leading to decreased grain yield. Intriguingly, the overexpression of a specific amino acid mutant of OsRopGEF10, designated gef10-W260S, was found to promote panicle development and grain yield. Further analysis using the BiFC assay revealed that the gef10-W260S mutation disrupted the recruitment of rice histidine phosphotransfer proteins (OsAHP1/2) to the plasma membrane (PM), thereby promoting cytokinin signaling. This effect was corroborated by a dark-induced leaf senescence assay, which revealed an increased cytokinin response in the gef10-W260S ectopic expression lines, whereas the overexpression lines presented a suppressed cytokinin response. Moreover, we revealed that the enhanced panicle development in the gef10-W260S lines was attributable to the upregulated expression of several type-B response regulators (RRs) that are crucial for panicle development. Collectively, these findings revealed the negative regulatory function of OsRopGEF10 in the development of the shoot apical meristem (SAM) via interference with cytokinin signaling. Our study highlights the promising role of OsRopGEF10 as a potential target for regulating SAM and panicle development in rice, revealing a valuable breeding strategy for increasing crop yield.
期刊介绍:
Rice aims to fill a glaring void in basic and applied plant science journal publishing. This journal is the world''s only high-quality serial publication for reporting current advances in rice genetics, structural and functional genomics, comparative genomics, molecular biology and physiology, molecular breeding and comparative biology. Rice welcomes review articles and original papers in all of the aforementioned areas and serves as the primary source of newly published information for researchers and students in rice and related research.