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


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.

SUBMITTER: Pijuan-Sala B 

PROVIDER: S-EPMC7145456 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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

Pijuan-Sala Blanca B   Wilson Nicola K NK   Xia Jun J   Hou Xiaomeng X   Hannah Rebecca L RL   Kinston Sarah S   Calero-Nieto Fernando J FJ   Poirion Olivier O   Preissl Sebastian S   Liu Feng F   Göttgens Berthold B  

Nature cell biology 20200330 4


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 usin  ...[more]

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