{"title":"osbrk1介导的OsPFN2磷酸化调节减数分裂纺锤体肌动蛋白组装和水稻育性。","authors":"Hai Zheng, Zhigang Zhao, Shanshan Zhu, Yulong Ren, Jiangfeng Shen, Ziqi Xun, Xiaowen Yu, Chaolong Wang, Bowen Yao, Siqi Cheng, Yang Hu, Shihao Zhang, Qiming Wang, Jiayu Lu, Zhenwei Xie, Dekun Lei, Anqi Jian, Minrui Chen, Keyi Chen, Shijia Liu, Xi Liu, Yunlu Tian, Lin Jiang, Zhijun Cheng, Cailin Lei, Qibing Lin, Xiupin Guo, Xin Wang, Chuanyin Wu, Haiyang Wang, Shanjin Huang, Jianmin Wan","doi":"10.1016/j.xplc.2025.101417","DOIUrl":null,"url":null,"abstract":"<p><p>Formation of a meiotic spindle structure is crucial for chromosome segregation and fertility in plants. Previous studies have shown that actin decorates spindle microtubules in mammalian oocytes, forming spindle actin, which is indispensable for genome stability and gamete segregation. However, the regulatory mechanisms that underlie spindle-actin assembly remain unknown. Here, we report that dysfunction of OsPFN2, a rice profilin protein, disrupts meiotic spindle-actin assembly and spindle microtubule structure and causes errors in chromosome alignment and segregation in pollen mother cells, resulting in male sterility. Furthermore, our results demonstrate that OsPFN2 interacts with Rice Morphology Determinant (OsRMD), a rice formin protein whose depletion also affects spindle-actin assembly and the structure of meiotic spindle microtubules. Intriguingly, we identified an interaction between OsPFN2 and Bub1-Related Kinase 1 (OsBRK1) and demonstrated that OsBRK1 depletion enhances spindle-actin assembly. In addition, we found that OsBRK1 phosphorylates OsPFN2 and that the resulting phosphorylated OsPFN2 retains its capability to bind actin. However, these phospho-mimetic actin-OsPFN2 complexes are not used by OsRMD. Our findings thus reveal that the OsPFN2-OsRMD module controls the assembly of meiotic spindle actin and that OsBRK1 fine-tunes this process through phosphorylation of OsPFN2.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":" ","pages":"101417"},"PeriodicalIF":11.6000,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12365840/pdf/","citationCount":"0","resultStr":"{\"title\":\"OsBRK1-mediated phosphorylation of OsPFN2 regulates meiotic spindle-actin assembly and rice fertility.\",\"authors\":\"Hai Zheng, Zhigang Zhao, Shanshan Zhu, Yulong Ren, Jiangfeng Shen, Ziqi Xun, Xiaowen Yu, Chaolong Wang, Bowen Yao, Siqi Cheng, Yang Hu, Shihao Zhang, Qiming Wang, Jiayu Lu, Zhenwei Xie, Dekun Lei, Anqi Jian, Minrui Chen, Keyi Chen, Shijia Liu, Xi Liu, Yunlu Tian, Lin Jiang, Zhijun Cheng, Cailin Lei, Qibing Lin, Xiupin Guo, Xin Wang, Chuanyin Wu, Haiyang Wang, Shanjin Huang, Jianmin Wan\",\"doi\":\"10.1016/j.xplc.2025.101417\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Formation of a meiotic spindle structure is crucial for chromosome segregation and fertility in plants. Previous studies have shown that actin decorates spindle microtubules in mammalian oocytes, forming spindle actin, which is indispensable for genome stability and gamete segregation. However, the regulatory mechanisms that underlie spindle-actin assembly remain unknown. Here, we report that dysfunction of OsPFN2, a rice profilin protein, disrupts meiotic spindle-actin assembly and spindle microtubule structure and causes errors in chromosome alignment and segregation in pollen mother cells, resulting in male sterility. Furthermore, our results demonstrate that OsPFN2 interacts with Rice Morphology Determinant (OsRMD), a rice formin protein whose depletion also affects spindle-actin assembly and the structure of meiotic spindle microtubules. Intriguingly, we identified an interaction between OsPFN2 and Bub1-Related Kinase 1 (OsBRK1) and demonstrated that OsBRK1 depletion enhances spindle-actin assembly. In addition, we found that OsBRK1 phosphorylates OsPFN2 and that the resulting phosphorylated OsPFN2 retains its capability to bind actin. However, these phospho-mimetic actin-OsPFN2 complexes are not used by OsRMD. Our findings thus reveal that the OsPFN2-OsRMD module controls the assembly of meiotic spindle actin and that OsBRK1 fine-tunes this process through phosphorylation of OsPFN2.</p>\",\"PeriodicalId\":52373,\"journal\":{\"name\":\"Plant Communications\",\"volume\":\" \",\"pages\":\"101417\"},\"PeriodicalIF\":11.6000,\"publicationDate\":\"2025-08-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12365840/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Communications\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.xplc.2025.101417\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/13 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Communications","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.xplc.2025.101417","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/13 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
OsBRK1-mediated phosphorylation of OsPFN2 regulates meiotic spindle-actin assembly and rice fertility.
Formation of a meiotic spindle structure is crucial for chromosome segregation and fertility in plants. Previous studies have shown that actin decorates spindle microtubules in mammalian oocytes, forming spindle actin, which is indispensable for genome stability and gamete segregation. However, the regulatory mechanisms that underlie spindle-actin assembly remain unknown. Here, we report that dysfunction of OsPFN2, a rice profilin protein, disrupts meiotic spindle-actin assembly and spindle microtubule structure and causes errors in chromosome alignment and segregation in pollen mother cells, resulting in male sterility. Furthermore, our results demonstrate that OsPFN2 interacts with Rice Morphology Determinant (OsRMD), a rice formin protein whose depletion also affects spindle-actin assembly and the structure of meiotic spindle microtubules. Intriguingly, we identified an interaction between OsPFN2 and Bub1-Related Kinase 1 (OsBRK1) and demonstrated that OsBRK1 depletion enhances spindle-actin assembly. In addition, we found that OsBRK1 phosphorylates OsPFN2 and that the resulting phosphorylated OsPFN2 retains its capability to bind actin. However, these phospho-mimetic actin-OsPFN2 complexes are not used by OsRMD. Our findings thus reveal that the OsPFN2-OsRMD module controls the assembly of meiotic spindle actin and that OsBRK1 fine-tunes this process through phosphorylation of OsPFN2.
期刊介绍:
Plant Communications is an open access publishing platform that supports the global plant science community. It publishes original research, review articles, technical advances, and research resources in various areas of plant sciences. The scope of topics includes evolution, ecology, physiology, biochemistry, development, reproduction, metabolism, molecular and cellular biology, genetics, genomics, environmental interactions, biotechnology, breeding of higher and lower plants, and their interactions with other organisms. The goal of Plant Communications is to provide a high-quality platform for the dissemination of plant science research.