Single-cell RNA-seq uncovers dynamic processes orchestrated by RNA-binding protein DDX43 in chromatin remodeling during spermiogenesis

• Published in: Nature communications Vol. 14; no. 1; p. 2499
• Main Authors: Tan, Huanhuan, Wang, Weixu, Zhou, Congjin, Wang, Yanfeng, Zhang, Shu, Yang, Pinglan, Guo, Rui, Chen, Wei, Zhang, Jinwen, Ye, Lan, Cui, Yiqiang, Ni, Ting, Zheng, Ke
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 29.04.2023; Nature Publishing Group UK; Nature Portfolio
• Subjects: Animals; Chromatin; Chromatin Assembly and Disassembly; Chromatin remodeling; Crosslinking; DEAD-box RNA Helicases - genetics; Differentiation; DNA helicase; Gene sequencing; Germ cells; Histones; Immunoprecipitation; Infertility; Male; Males; Meiosis; Mice; Mice, Knockout; Missense mutation; Phenotypes; Proteins; Ribonucleic acid; RNA; RNA helicase; RNA-binding protein; RNA-Binding Proteins - genetics; Single-Cell Gene Expression Analysis; Spermatids; Spermatogenesis; Spermatogenesis - genetics; Spermiogenesis; Switches; Transcriptomics
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-023-38199-w

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.