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Single-cell chromatin accessibility maps reveal regulatory programs driving early mouse organogenesis.

Authors :
Pijuan-Sala B
Wilson NK
Xia J
Hou X
Hannah RL
Kinston S
Calero-Nieto FJ
Poirion O
Preissl S
Liu F
Göttgens B
Source :
Nature cell biology [Nat Cell Biol] 2020 Apr; Vol. 22 (4), pp. 487-497. Date of Electronic Publication: 2020 Mar 30.
Publication Year :
2020

Abstract

During mouse embryonic development, pluripotent cells rapidly divide and diversify, yet the regulatory programs that define the cell repertoire for each organ remain ill-defined. To delineate comprehensive chromatin landscapes during early organogenesis, we mapped chromatin accessibility in 19,453 single nuclei from mouse embryos at 8.25 days post-fertilization. Identification of cell-type-specific regions of open chromatin pinpointed two TAL1-bound endothelial enhancers, which we validated using transgenic mouse assays. Integrated gene expression and transcription factor motif enrichment analyses highlighted cell-type-specific transcriptional regulators. Subsequent in vivo experiments in zebrafish revealed a role for the ETS factor FEV in endothelial identity downstream of ETV2 (Etsrp in zebrafish). Concerted in vivo validation experiments in mouse and zebrafish thus illustrate how single-cell open chromatin maps, representative of a mammalian embryo, provide access to the regulatory blueprint for mammalian organogenesis.

Details

Language :
English
ISSN :
1476-4679
Volume :
22
Issue :
4
Database :
MEDLINE
Journal :
Nature cell biology
Publication Type :
Academic Journal
Accession number :
32231307
Full Text :
https://doi.org/10.1038/s41556-020-0489-9