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Critical role of the BAF chromatin remodeling complex during murine neural crest development.
- Source :
-
PLoS genetics [PLoS Genet] 2021 Mar 22; Vol. 17 (3), pp. e1009446. Date of Electronic Publication: 2021 Mar 22 (Print Publication: 2021). - Publication Year :
- 2021
-
Abstract
- The BAF complex plays an important role in the development of a wide range of tissues by modulating gene expression programs at the chromatin level. However, its role in neural crest development has remained unclear. To determine the role of the BAF complex, we deleted BAF155/BAF170, the core subunits required for the assembly, stability, and functions of the BAF complex in neural crest cells (NCCs). Neural crest-specific deletion of BAF155/BAF170 leads to embryonic lethality due to a wide range of developmental defects including craniofacial, pharyngeal arch artery, and OFT defects. RNAseq and transcription factor enrichment analysis revealed that the BAF complex modulates the expression of multiple signaling pathway genes including Hippo and Notch, essential for the migration, proliferation, and differentiation of the NCCs. Furthermore, we demonstrated that the BAF complex is essential for the Brg1-Yap-Tead-dependent transcription of target genes in NCCs. Together, our results demonstrate an important role of the BAF complex in modulating the gene regulatory network essential for neural crest development.<br />Competing Interests: The authors have declared that no competing interests exist.
- Subjects :
- Animals
Cell Differentiation genetics
Cell Proliferation
DNA-Binding Proteins metabolism
Embryonic Development genetics
Gene Deletion
Gene Regulatory Networks
Genes, Reporter
Mice
Mice, Transgenic
Organ Specificity
Transcription Factors genetics
Transcription Factors metabolism
Transcription, Genetic
Chromatin Assembly and Disassembly
DNA-Binding Proteins genetics
Gene Expression Regulation, Developmental
Neural Crest embryology
Neural Crest metabolism
Neurogenesis genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1553-7404
- Volume :
- 17
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- PLoS genetics
- Publication Type :
- Academic Journal
- Accession number :
- 33750945
- Full Text :
- https://doi.org/10.1371/journal.pgen.1009446