PUBLICATION
            Drl.3 governs primitive hematopoiesis in zebrafish
- Authors
- Pimtong, W., Datta, M., Ulrich, A.M., Rhodes, J.
- ID
- ZDB-PUB-140724-10
- Date
- 2014
- Source
- Scientific Reports 4: 5791 (Journal)
- Registered Authors
- Datta, Madhusmita, Pimtong, Wittaya, Rhodes, Jennifer
- Keywords
- Cell biology, Haematopoiesis
- MeSH Terms
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                - RNA, Messenger/genetics
- Antibody Formation
- Zebrafish/embryology
- Zebrafish/physiology*
- Cell Lineage
- Humans
- Reverse Transcriptase Polymerase Chain Reaction
- Gene Expression Regulation, Developmental
- Embryo, Nonmammalian/cytology
- Embryo, Nonmammalian/physiology*
- Zebrafish Proteins/genetics
- Zebrafish Proteins/immunology
- Zebrafish Proteins/metabolism*
- Animals
- Hematopoiesis/physiology*
- Rabbits
- Erythropoiesis/physiology*
- Cell Differentiation*
- HEK293 Cells
- In Situ Hybridization
- Hematopoietic Stem Cells/cytology
- Hematopoietic Stem Cells/physiology*
- Real-Time Polymerase Chain Reaction
 
- PubMed
- 25051985 Full text @ Sci. Rep.
            Citation
        
        
            Pimtong, W., Datta, M., Ulrich, A.M., Rhodes, J. (2014) Drl.3 governs primitive hematopoiesis in zebrafish. Scientific Reports. 4:5791.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The molecular program controlling hematopoietic differentiation is not fully understood. Here, we describe a family of zebrafish genes that includes a novel hematopoietic regulator, draculin-like 3 (drl.3). We found that drl.3 is expressed in mesoderm-derived hematopoietic cells and is retained during erythroid maturation. Moreover, drl.3 expression correlated with erythroid development in gata1a- and spi1b-depleted embryos. Loss-of-function analysis indicated that drl.3 plays an essential role in primitive erythropoiesis and, to a lesser extent, myelopoiesis that is independent of effects on vasculature, emergence of primitive and definitive progenitor cells and cell viability. While drl.3 depletion reduced gata1a expression and inhibited erythroid development, enforced expression of gata1a was not sufficient to rescue erythropoiesis, indicating that the regulation of hematopoiesis by drl.3 extends beyond control of gata1a expression. Knockdown of drl.3 increased the proportion of less differentiated, primitive hematopoietic cells without affecting proliferation, establishing drl.3 as an important regulator of primitive hematopoietic cell differentiation.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    