PUBLICATION
            The Paf1 Complex and P-TEFb have reciprocal and antagonist roles in maintaining multipotent neural crest progenitors
- Authors
- Jurynec, M.J., Bai, X., Bisgrove, B.W., Jackson, H., Nechiporuk, A., Palu, R.A.S., Grunwald, H.A., Su, Y.C., Hoshijima, K., Yost, H.J., Zon, L.I., Grunwald, D.J.
- ID
- ZDB-PUB-191201-2
- Date
- 2019
- Source
- Development (Cambridge, England) 146(24): (Journal)
- Registered Authors
- Bai, Xiaoying, Bisgrove, Brent, Grunwald, David, Hoshijima, Kazuyuki, Jurynec, Michael, Nechiporuk, Alex, Yost, H. Joseph, Zon, Leonard I.
- Keywords
- Neural crest, Paf1 Complex, Stem cells, Transcription pausing, Zebrafish mutant
- MeSH Terms
- 
    
        
        
            
                - Body Patterning/genetics
- Animals
- Embryo, Nonmammalian
- Multipotent Stem Cells/cytology
- Multipotent Stem Cells/physiology*
- Positive Transcriptional Elongation Factor B/antagonists & inhibitors
- Positive Transcriptional Elongation Factor B/metabolism
- Positive Transcriptional Elongation Factor B/physiology*
- Neural Stem Cells/cytology
- Neural Stem Cells/physiology*
- Cell Lineage/genetics*
- Cyclin-Dependent Kinase 9/genetics
- Cell Differentiation/genetics
- Neural Crest/cytology*
- Neural Crest/physiology
- Multiprotein Complexes/antagonists & inhibitors
- Multiprotein Complexes/metabolism
- Multiprotein Complexes/physiology
- RNA Polymerase II/metabolism
- Zebrafish/embryology
- Zebrafish/genetics
- Gene Expression Regulation, Developmental
- Nuclear Proteins/antagonists & inhibitors
- Nuclear Proteins/metabolism
- Nuclear Proteins/physiology*
- Animals, Genetically Modified
 
- PubMed
- 31784460 Full text @ Development
            Citation
        
        
            Jurynec, M.J., Bai, X., Bisgrove, B.W., Jackson, H., Nechiporuk, A., Palu, R.A.S., Grunwald, H.A., Su, Y.C., Hoshijima, K., Yost, H.J., Zon, L.I., Grunwald, D.J. (2019) The Paf1 Complex and P-TEFb have reciprocal and antagonist roles in maintaining multipotent neural crest progenitors. Development (Cambridge, England). 146(24):.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Multipotent progenitor populations are necessary for generating diverse tissue types during embryogenesis. We show the Polymerase Associated Factor 1 Complex (Paf1C) is required to maintain multipotent progenitors of the neural crest (NC) lineage in zebrafish. Mutations affecting each Paf1C component result in near-identical NC phenotypes; alyron mutant embryos carrying a null mutation in paf1 were analyzed in detail. In the absence of zygotic paf1 function, definitive premigratory NC progenitors arise but fail to maintain expression of the sox10 specification gene. The mutant NC progenitors migrate aberrantly and fail to differentiate appropriately. Blood and germ cell progenitor development is affected similarly. Development of mutant NC could be rescued by additional loss of Positive Transcription Elongation Factor b (P-TEFb) activity, a key factor in promoting transcription elongation. Consistent with the interpretation that inhibiting/delaying expression of some genes is essential for maintaining progenitors, mutant embryos lacking the CDK9 kinase component of P-TEFb exhibit a surfeit of NC progenitors and their derivatives. We propose Paf1C and P-TEFb act antagonistically to regulate the timing of the expression of genes needed for NC development.
            
    
        
        
    
    
    
                
                    
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                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    