| Literature DB >> 33501917 |
Pengfei Xu1, Haoze V Yu1, Kuo-Chang Tseng1, Mackenzie Flath1, Peter Fabian1, Neil Segil1, J Gage Crump1.
Abstract
The specification of cartilage requires Sox9, a transcription factor with broad roles for organogenesis outside the skeletal system. How Sox9 and other factors gain access to cartilage-specific cis-regulatory regions during skeletal development was unknown. By analyzing chromatin accessibility during the differentiation of neural crest cells into chondrocytes of the zebrafish head, we find that cartilage-associated chromatin accessibility is dynamically established. Cartilage-associated regions that become accessible after neural crest migration are co-enriched for Sox9 and Fox transcription factor binding motifs. In zebrafish lacking Foxc1 paralogs, we find a global decrease in chromatin accessibility in chondrocytes, consistent with a later loss of dorsal facial cartilages. Zebrafish transgenesis assays confirm that many of these Foxc1-dependent elements function as enhancers with region- and stage-specific activity in facial cartilages. These results show that Foxc1 promotes chondrogenesis in the face by establishing chromatin accessibility at a number of cartilage-associated gene enhancers.Entities:
Keywords: Foxc1; Sox9; cartilage; chromosomes; cranial neural crest; craniofacial; developmental biology; epigenetics; gene expression; zebrafish
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Year: 2021 PMID: 33501917 PMCID: PMC7891931 DOI: 10.7554/eLife.63595
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140