| Literature DB >> 28803779 |
Shumeng Liu1, Huajing Yu2, Yongqing Liu2, Xinhua Liu3, Yu Zhang2, Chen Bu4, Shuai Yuan2, Zhe Chen2, Guojia Xie2, Wanjin Li2, Bosen Xu2, Jianguo Yang2, Lin He2, Tong Jin2, Yundong Xiong2, Luyang Sun2, Xiaohui Liu5, Chunsheng Han6, Zhongyi Cheng4, Jing Liang7, Yongfeng Shang8.
Abstract
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.Entities:
Keywords: CDYL; crotonyl-CoA hydratase; gene transcription; histone crotonylation; histone replacement; spermatogenesis
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Year: 2017 PMID: 28803779 DOI: 10.1016/j.molcel.2017.07.011
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970