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单细胞ATAC测序揭示了人类精子发生过程中细胞类型特异性转录调控和独特的染色质可及性。

Single-cell ATAC-Seq reveals cell type-specific transcriptional regulation and unique chromatin accessibility in human spermatogenesis.

作者信息

Wu Xiaolong, Lu Mujun, Yun Damin, Gao Sheng, Chen Shitao, Hu Longfei, Wu Yunhao, Wang Xiaorong, Duan Enkui, Cheng C Yan, Sun Fei

出版信息

Hum Mol Genet. 2022 Feb 3;31(3):321-333. doi: 10.1093/hmg/ddab006.

DOI:10.1093/hmg/ddab006
PMID:33438010
Abstract

During human spermatogenesis, germ cells undergo dynamic changes in chromatin organization/re-packaging and in transcriptomes. In order to better understand the underlying mechanism(s), scATAC-Seq of 5376 testicular cells from 3 normal men were performed. Data were analyzed in parallel with the scRNA-Seq data of human testicular cells. In all, 10 germ cell types associated with spermatogenesis and 6 testicular somatic cell types were identified, along with 142 024 peaks located in promoter, genebody and CpG Island. We had examined chromatin accessibility of all chromosomes, with chromosomes 19 and 17 emerged as the leading chromosomes that displayed high chromatin accessibility. In accessible chromatin regions, transcription factor-binding sites were identified and specific motifs with high frequencies at different spermatogenesis stages were detected, including CTCF, BORIS, NFY, DMRT6, EN1, ISL1 and GLI3. Two most remarkable observations were noted. First, TLE3 was specifically expressed in differentiating spermatogonia. Second, PFN4 was found to be involved in actin cytoskeletal organization during meiosis. More important, unique regions upstream of PFN4 and TLE3 were shown to display high accessibility, illustrating their significance in supporting human spermatogenesis.

摘要

在人类精子发生过程中,生殖细胞在染色质组织/重新包装和转录组方面经历动态变化。为了更好地理解其潜在机制,对来自3名正常男性的5376个睾丸细胞进行了单细胞染色质转座酶可及性测序(scATAC-Seq)。数据与人类睾丸细胞的单细胞RNA测序(scRNA-Seq)数据并行分析。总共鉴定出10种与精子发生相关的生殖细胞类型和6种睾丸体细胞类型,以及位于启动子、基因体和CpG岛的142024个峰。我们检查了所有染色体的染色质可及性,其中19号和17号染色体成为显示高染色质可及性的主要染色体。在可及的染色质区域,鉴定出转录因子结合位点,并检测到在不同精子发生阶段高频出现的特定基序,包括CTCF、BORIS、NFY、DMRT6、EN1、ISL1和GLI3。有两个最显著的发现。第一,TLE3在分化中的精原细胞中特异性表达。第二,发现PFN 在减数分裂过程中参与肌动蛋白细胞骨架组织。更重要的是,PFN4和TLE3上游的独特区域显示出高可及性,说明了它们在支持人类精子发生中的重要性。 4

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