生物
染色质
染色质重塑
细胞生物学
精子发生
生殖细胞
精子细胞
RNA解旋酶A
染色质免疫沉淀
转录组
核糖核酸
遗传学
基因
基因表达
解旋酶
发起人
核心
精子
作者
Huanhuan Tan,Weixu Wang,Congjin Zhou,Yanfeng Wang,Shu Zhang,Pinglan Yang,Rui Guo,Wei Chen,Jinwen Zhang,Lan Ye,Yiqiang Cui,Ting Ni,Ke Zheng
标识
DOI:10.1038/s41467-023-38199-w
摘要
Mammalian spermatogenesis shows prominent chromatin and transcriptomic switches in germ cells, but it is unclear how such dynamics are controlled. Here we identify RNA helicase DDX43 as an essential regulator of the chromatin remodeling process during spermiogenesis. Testis-specific Ddx43 knockout mice show male infertility with defective histone-to-protamine replacement and post-meiotic chromatin condensation defects. The loss of its ATP hydrolysis activity by a missense mutation replicates the infertility phenotype in global Ddx43 knockout mice. Single-cell RNA sequencing analyses of germ cells depleted of Ddx43 or expressing the Ddx43 ATPase-dead mutant reveals that DDX43 regulates dynamic RNA regulatory processes that underlie spermatid chromatin remodeling and differentiation. Transcriptomic profiling focusing on early-stage spermatids combined with enhanced crosslinking immunoprecipitation and sequencing further identifies Elfn2 as DDX43-targeted hub gene. These findings illustrate an essential role for DDX43 in spermiogenesis and highlight the single-cell-based strategy to dissect cell-state-specific regulation of male germline development.
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