OsMS1 functions as a transcriptional activator to regulate programmed tapetum development and pollen exine formation in rice
文献类型: 外文期刊
第一作者: Yang, Zhengfu
作者: Yang, Zhengfu;Liu, Ling;Sun, Lianping;Yu, Ping;Zhang, Peipei;Abbas, Adil;Xiang, Xiaojiao;Wu, Weixun;Zhang, Yingxin;Cao, Liyong;Cheng, Shihua;Yang, Zhengfu;Liu, Ling;Sun, Lianping;Yu, Ping;Zhang, Peipei;Abbas, Adil;Xiang, Xiaojiao;Wu, Weixun;Zhang, Yingxin;Cao, Liyong;Cheng, Shihua;Yang, Zhengfu;Zhang, Peipei;Xiang, Xiaojiao
作者机构:
关键词: Rice; Male sterility; OsMS1; Tapetum PCD; Pollen exine
期刊名称:PLANT MOLECULAR BIOLOGY ( 影响因子:4.076; 五年影响因子:4.89 )
ISSN: 0167-4412
年卷期: 2019 年 99 卷 1-2 期
页码:
收录情况: SCI
摘要: OsMS1 functions as a transcriptional activator and interacts with known tapetal regulatory factors through its plant homeodomain (PHD) regulating tapetal programmed cell death (PCD) and pollen exine formation in rice. The tapetum, a hallmark tissue in the stamen, undergoes degradation triggered by PCD during post-meiotic anther development. This degradation process is indispensable for anther cuticle and pollen exine formation. Previous study has shown that PTC1 plays a critical role in the regulation of tapetal PCD. However, it remained unclear how this occurs. To further investigate the role of this gene in rice, we used CRISPR/Cas9 system to generate the homozygous mutant named as osms1, which showed complete male sterility with slightly yellow and small anthers, as well as invisible pollen grains. In addition, cytological observation revealed delayed tapetal PCD, defective pollen exine formation and a lack of DNA fragmentation according to a TUNEL analysis in the anthers of osms1 mutant. OsMS1, which encodes a PHD finger protein, was located in the nucleus of rice protoplasts and functioned as a transcription factor with transcriptional activation activity. Y2H and BiFC assays demonstrated that OsMS1 can interact with OsMADS15 and TDR INTERACTING PROTEIN2 (TIP2). It has been reported that TIP2 coordinated with TDR to modulate the expression of EAT1 and further regulated tapetal PCD in rice. Results of qPCR suggested that the expression of the genes associated with tapetal PCD and pollen wall biosynthesis, such as EAT1, AP37, AP25, OsC6 and OsC4, were significantly reduced in osms1 mutant. Taken together, our results demonstrate that the interaction of OsMS1 with known tapetal regulatory factors through its PHD finger regulates tapetal PCD and pollen exine formation in rice.
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