Feedback Regulation of DYT1 by Interactions with Downstream bHLH Factors Promotes DYT1 Nuclear Localization and Anther Development

被引:88
作者
Cui, Jie [1 ,2 ,3 ,4 ]
You, Chenjiang [1 ,2 ,3 ,4 ]
Zhu, Engao [1 ,2 ,3 ,4 ]
Huang, Qiang [1 ,2 ,4 ]
Ma, Hong [1 ,2 ,3 ,5 ]
Chang, Fang [1 ,2 ,3 ,4 ]
机构
[1] Fudan Univ, State Key Lab Genet Engn, Shanghai 200438, Peoples R China
[2] Fudan Univ, Sch Life Sci, Collaborat Innovat Ctr Genet & Dev, Shanghai 200438, Peoples R China
[3] Fudan Univ, Minist Educ, Key Lab Biodivers Sci & Ecol Engn, Shanghai 200438, Peoples R China
[4] Fudan Univ, Sch Life Sci, Inst Biodivers Sci, Inst Plant Biol, Shanghai 200438, Peoples R China
[5] Fudan Univ, Inst Biomed Sci, Ctr Evolutionary Biol, Shanghai 200438, Peoples R China
基金
中国国家自然科学基金;
关键词
POLLEN WALL FORMATION; TRANSCRIPTION FACTOR; CELL FATE; TAPETUM DEVELOPMENT; CRYSTAL-STRUCTURE; ARABIDOPSIS; RICE; DOMAIN; SPECIFICITY; RECOGNITION;
D O I
10.1105/tpc.15.00986
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcriptional regulation is one of the most important mechanisms controlling development and cellular functions in plants and animals. The Arabidopsis thaliana bHLH transcription factor (TF) DYSFUNCTIONL TAPETUM1 (DYT1) is required for normal male fertility and anther development and activates the expression of the bHLH010/bHLH089/bHLH091 genes. Here, we showed that DYT1 is localized to both the cytoplasm and nucleus at anther stage 5 but specifically to the nucleus at anther stage 6 and onward. The bHLH010/bHLH089/bHLH091 proteins have strong nuclear localization signals, interact with DYT1, and facilitate the nuclear localization of DYT1. We further found that the conserved C-terminal BIF domain of DYT1 is required for its dimerization, nuclear localization, transcriptional activation activity, and function in anther development. Interestingly, when the BIF domain of DYT1 was replaced with that of bHLH010, the DYT1N-bHLH010BIF chimeric protein shows nuclear-preferential localization at anther stage 5 but could not fully rescue the dyt1-3 phenotype, suggesting that the normal spatio-temporal subcellular localization of DYT1 is important for DYT1 function and/or that the BIF domains from different bHLH members might be functionally distinct. Our results support an important positive feedback regulatory mechanism whereby downstream TFs increase the function of an upstream TF by enhancing its nucleus localization through the BIF domain.
引用
收藏
页码:1078 / 1093
页数:16
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