生物
体细胞
染色质
电池类型
表观遗传学
生殖细胞
生殖系
转录因子
遗传学
细胞命运测定
基因表达调控
支持细胞
基因
细胞
细胞生物学
精子发生
内分泌学
作者
Jinyue Liao,Hoi Ching Suen,Shitao Rao,Alfred Chun Shui Luk,Ruoyu Zhang,Annie Wing-Tung Lee,Ting Hei Thomas Chan,Man Yee Cheung,David H. Chu,Hon‐Cheong So,Robin M. Hobbs,TL Lee
标识
DOI:10.1101/2021.03.17.435776
摘要
Abstract Spermatogenesis depends on an orchestrated series of developing events in germ cells and full maturation of the somatic microenvironment. To date, the majority of efforts to study cellular heterogeneity in testis has been focused on single-cell gene expression rather than the chromatin landscape shaping gene expression. To advance our understanding of the regulatory programs underlying testicular cell types, we analyzed single-cell chromatin accessibility profiles in more than 25,000 cells from mouse developing testis. We showed that scATAC-Seq allowed us to deconvolve distinct cell populations and identify cis-regulatory elements (CREs) underlying cell type specification. We identified sets of transcription factors associated with cell type-specific accessibility, revealing novel regulators of cell fate specification and maintenance. Pseudotime reconstruction revealed detailed regulatory dynamics coordinating the sequential developmental progressions of germ cells and somatic cells. This high-resolution data also revealed putative stem cells within the Sertoli and Leydig cell populations. Further, we defined candidate target cell types and genes of several GWAS signals, including those associated with testosterone levels and coronary artery disease. Collectively, our data provide a blueprint of the ‘regulon’ of the mouse male germline and supporting somatic cells.
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