EMBRYONIC FLOWER 1 通过抑制茉莉酸盐通路下游转录因子 MYB26 来调节雄性繁殖

Zhijuan Chen, Jing Lu, Xiaoyi Li, Danhua Jiang, Zicong Li
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引用次数: 0

摘要

进化保守的多聚核酸抑制复合体(PRC)介导全基因组转录沉默,调控多细胞生物的大量发育和环境反应。PRC2 催化的组蛋白 H3 上赖氨酸 27 的三甲基化(H3K27me3)被 PRC1 的阅读器效应模块识别,从而实现基因抑制。在这里,我们报告了拟南芥(Arabidopsis thaliana)H3K27me3效应因子EMBRYONIC FLOWER 1(EMF1)与R2R3 DNA结合转录因子MYB26相互作用,并通过雄蕊中的一个雌花保守基团对其进行限制。MYB26 可激活两个 NAC 结构域基因 NAC 次级壁增厚促进因子 1(NST1)和 NST2 的转录,这两个基因编码的蛋白质在茉莉酸盐(JA)调控的雄蕊成熟过程中介导花药次级细胞增厚。在这一过程中,MYB26 的转录活性受到 JAZ-PRC 抑制复合体的负调控,从而精确调节 NST1 和 NST2 的表达。EMF1 抑制的中断会刺激 MYB26,导致两个 NAC 基因的过度转录和雄性不育。我们的研究结果揭示了多聚酶介导的基因沉默的新机制,并说明植物多聚酶复合体通过防止雄性繁殖中JA反应的超敏性来调控雄蕊的发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EMBRYONIC FLOWER 1 regulates male reproduction by repressing the jasmonate pathway downstream transcription factor MYB26
The evolutionarily conserved Polycomb repressive complexes (PRC) mediate genome-wide transcriptional silencing and regulate a plethora of development, as well as environmental responses in multicellular organisms. The PRC2-catalyzed trimethylation of lysine 27 on histone H3 (H3K27me3) is recognized by reader-effector modules of PRC1 to implement gene repression. Here, we report that the Arabidopsis (Arabidopsis thaliana) H3K27me3 effector EMBRYONIC FLOWER 1 (EMF1) interacts with and constrains the R2R3 DNA binding transcription factor MYB26 by a eudicot-conserved motif in the stamen. MYB26 activates the transcription of two NAC domain genes, NAC SECONDARY WALL THICKENING PROMOTING FACTOR1 (NST1) and NST2, whose encoded proteins mediate anther secondary cell thickening in jasmonate (JA)-regulated stamen maturation. In this process, the transcriptional activity of MYB26 is negatively modulated by the JAZ-PRC repressive complex to precisely regulate the expression of NST1 and NST2. Disruption of EMF1 repression stimulates MYB26, leading to the excessive transcription of the two NAC genes and male sterility. Our results reveal a novel mechanism in polycomb-mediated gene silencing and illustrate that the plant Polycomb complex regulates stamen development by preventing the hypersensitivity of JA responses in male reproduction.
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