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Single-cell chromatin accessibility maps reveal regulatory programs driving early mouse organogenesis.
- 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.
- Subjects :
- Animals
Cell Lineage genetics
Cell Nucleus genetics
Cell Nucleus metabolism
Chromatin metabolism
Embryo, Mammalian
Embryo, Nonmammalian
Embryonic Development
Endothelial Cells cytology
Gene Expression Profiling
Mice
Mice, Transgenic
Organ Specificity
Protein Binding
Single-Cell Analysis
T-Cell Acute Lymphocytic Leukemia Protein 1 metabolism
Transcription Factors genetics
Transcription Factors metabolism
Transcription, Genetic
Zebrafish
Zebrafish Proteins genetics
Zebrafish Proteins metabolism
Chromatin chemistry
Endothelial Cells metabolism
Enhancer Elements, Genetic
Gene Expression Regulation, Developmental
Organogenesis genetics
T-Cell Acute Lymphocytic Leukemia Protein 1 genetics
Subjects
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