Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China; Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Capital Medical University, Beijing 100069, China.
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China.
Mol Cell. 2017 Sep 7;67(5):853-866.e5. doi: 10.1016/j.molcel.2017.07.011. Epub 2017 Aug 10.
Lysine crotonylation (Kcr) is a newly identified histone modification that is associated with active transcription in mammalian cells. Here we report that the chromodomain Y-like transcription corepressor CDYL negatively regulates histone Kcr by acting as a crotonyl-CoA hydratase to convert crotonyl-CoA to β-hydroxybutyryl-CoA. We showed that the negative regulation of histone Kcr by CDYL is intrinsically linked to its transcription repression activity and functionally implemented in the reactivation of sex chromosome-linked genes in round spermatids and genome-wide histone replacement in elongating spermatids. Significantly, Cdyl transgenic mice manifest dysregulation of histone Kcr and reduction of male fertility with a decreased epididymal sperm count and sperm cell motility. Our study uncovers a biochemical pathway in the regulation of histone Kcr and implicates CDYL-regulated histone Kcr in spermatogenesis, adding to the understanding of the physiology of male reproduction and the mechanism of the spermatogenic failure in AZFc (Azoospermia Factor c)-deleted infertile men.
赖氨酸丁酰化(Kcr)是一种新发现的组蛋白修饰,与哺乳动物细胞中活跃的转录有关。在这里,我们报告说,类染色质域 Y 相关转录核心抑制因子 CDYL 通过作为丙二酰辅酶 A 水合酶来负调控组蛋白 Kcr,将丙二酰辅酶 A 转化为β-羟基丁酰辅酶 A。我们表明,CDYL 对组蛋白 Kcr 的负调控与其转录抑制活性内在相关,并在圆形精子细胞中性染色体连接基因的重新激活和延长精子细胞中全基因组组蛋白替换中得到功能实现。重要的是,Cdyl 转基因小鼠表现出组蛋白 Kcr 的失调和精子活力降低,附睾精子计数减少。我们的研究揭示了组蛋白 Kcr 调控的生化途径,并表明 CDYL 调节的组蛋白 Kcr 在精子发生中起作用,这增加了对男性生殖生理学的理解和 AZFc(无精子症因子 c)缺失不育男性精子发生失败的机制。