PUBLICATION
            The alx3 gene shapes the zebrafish neurocranium by regulating frontonasal neural crest cell differentiation timing
- Authors
- Mitchell, J.M., Sucharov, J., Pulvino, A.T., Brooks, E.P., Gillen, A.E., Nichols, J.T.
- ID
- ZDB-PUB-210321-4
- Date
- 2021
- Source
- Development (Cambridge, England) 148(7): (Journal)
- Registered Authors
- Brooks, Elliott, Nichols, James Tucker
- Keywords
- Bone, Cartilage, Craniofacial skeleton, Differentiation, Neural crest cells, Neurocranium, Zebrafish, alx, scRNA-seq
- Datasets
- GEO:GSE163826
- MeSH Terms
- 
    
        
        
            
                - Animals
- Transcription Factors/genetics
- Transcriptome
- Homeodomain Proteins/genetics*
- Homeodomain Proteins/metabolism*
- Gene Expression Regulation, Developmental
- Organogenesis
- Cell Differentiation/genetics*
- Cell Differentiation/physiology
- Morphogenesis
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism*
- Mice, Transgenic
- Head
- Zebrafish/embryology
- Zebrafish/genetics*
- Zebrafish/metabolism*
- Cartilage/metabolism
- Neural Crest/cytology
- Neural Crest/metabolism*
- Skull/metabolism
 
- PubMed
- 33741714 Full text @ Development
            Citation
        
        
            Mitchell, J.M., Sucharov, J., Pulvino, A.T., Brooks, E.P., Gillen, A.E., Nichols, J.T. (2021) The alx3 gene shapes the zebrafish neurocranium by regulating frontonasal neural crest cell differentiation timing. Development (Cambridge, England). 148(7):.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                During craniofacial development, different populations of cartilage and bone forming cells develop in precise locations in the head. Most of these cells are derived from pluripotent cranial neural crest cells and differentiate with distinct developmental timing and cellular morphologies. The mechanisms that divide neural crest cells into discrete populations are not fully understood. Here we use single-cell RNA sequencing to transcriptomically define different populations of cranial neural crest cells. We discovered that the transcription factor encoding alx gene family is enriched in the frontonasal population of neural crest cells. Genetic mutant analyses indicate that alx3 functions to regulate the distinct differentiation timing and cellular morphologies among frontonasal neural crest cell subpopulations. This study furthers our understanding of how genes controlling developmental timing shape craniofacial skeletal elements.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    