PUBLICATION
Med14 cooperates with brg1 in the differentiation of skeletogenic neural crest
- Authors
- Lou, X., Burrows, J.T., Scott, I.C.
- ID
- ZDB-PUB-151111-3
- Date
- 2015
- Source
- BMC Developmental Biology 15: 41 (Journal)
- Registered Authors
- Burrows, Jeff, Lou, Xin, Scott, Ian
- Keywords
- Neural crest, Mediator complex, BAF complex, Brg1, Craniofacial defect, Med14, Jaw development
- MeSH Terms
-
- Zebrafish/embryology*
- Jaw Abnormalities/genetics
- Maxillofacial Development/genetics*
- Maxillofacial Development/physiology
- Cell Proliferation
- PubMed
- 26553192 Full text @ BMC Dev. Biol.
Abstract
Background An intricate gene regulatory network drives neural crest migration and differentiation. How epigenetic regulators contribute to this process is just starting to be understood.
Results We found that mutation of med14 or brg1 in zebrafish embryos resulted in a cluster of neural crest cell-related defects. In med14 or brg1 mutants, neural crest cells that form the jaw skeleton were specified normally and migrated to target sites. However, defects in their subsequent terminal differentiation were evident. Transplantation experiments demonstrated that med14 and brg1 are required directly in neural crest cells. Analysis of med14; brg1 double mutant embryos suggested the existence of a strong genetic interaction between members of the Mediator and BAF complexes.
Conclusions These results suggest a critical role for Mediator and BAF complex function in neural crest development, and may also clarify the nature of defects in some craniofacial abnormalities.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping