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

单细胞染色质可及性图谱揭示了驱动小鼠早期器官发生的调控程序

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作者:Pijuan-Sala Blanca, Wilson Nicola K, Xia Jun, Hou Xiaomeng, Hannah Rebecca L, Kinston Sarah, Calero-Nieto Fernando J, Poirion Olivier, Preissl Sebastian, Liu Feng, Göttgens Berthold
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.

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