The single-cell chromatin accessibility landscape in mouse perinatal testis development
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 dataset also unveiled previously unreported subpopulations within both the Sertoli and Leydig cell groups. 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.
Data availability
All raw and processed sequencing data generated in this study have been submitted to the NCBI Gene Expression Omnibus (GEO; https://www.ncbi.nlm.nih.gov/geo/) under accession number GSE164439. Code for producing the majority of analyses from this paper is available on GitHub at https://github.com/liaojinyue/mouse_testis_scATAC.
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Genome-wide maps of chromatin state in mouse perinatal testes [scATAC-seq]NCBI Gene Expression Omnibus, GSE164439.
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Single-cell RNAseq analysis of testicular germ and somatic cell development during the perinatal periodNCBI Gene Expression Omnibus, GSE130593.
Article and author information
Author details
Funding
Chinese University of Hong Kong (Department of Chemical Pathology's Faculty Startup Fund)
- Jinyue Liao
University Grants Committee (General Research Fund CUHK 14120418)
- Tin-lap Lee
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Reviewing Editor
- Deborah Bourc'his, Institut Curie, France
Ethics
Animal experimentation: All the animal experiments were performed according to the protocols approved by the Animal Experiment Ethics Committee (AEEC) of The Chinese University of Hong Kong (CUHK) and followed the Animals (Control of Experiments) Ordinance (Cap. 340) licensed from the Department of Health, the Government of Hong Kong Special Administrative Region.
Version history
- Preprint posted: March 17, 2021 (view preprint)
- Received: November 16, 2021
- Accepted: April 24, 2023
- Accepted Manuscript published: April 25, 2023 (version 1)
- Accepted Manuscript updated: April 27, 2023 (version 2)
- Version of Record published: May 11, 2023 (version 3)
Copyright
© 2023, Suen et al.
This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.
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Further reading
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