PUBLICATION
            Molecular cloning, genetic mapping, and expression analysis of four zebrafish c/ebp genes
- Authors
 - Lyons, S.E., Shue, B.C., Lei, L., Oates, A.C., Zon, L.I., and Liu, P.P.
 - ID
 - ZDB-PUB-020102-2
 - Date
 - 2001
 - Source
 - Gene 281(1-2): 43-51 (Journal)
 - Registered Authors
 - Liu, Pu Paul, Lyons, Susan, Oates, Andrew, Zon, Leonard I.
 - Keywords
 - Danio rerio; hematopoietic; CCAAT/enhancer binding protein; liver; adipocyte
 - MeSH Terms
 - 
    
        
        
            
                
- Molecular Sequence Data
 - Embryo, Nonmammalian/metabolism
 - Protein Isoforms
 - In Situ Hybridization
 - Amino Acid Sequence
 - Cloning, Molecular
 - Chromosome Mapping
 - CCAAT-Enhancer-Binding Protein-alpha/genetics
 - Mutation
 - Sequence Homology, Amino Acid
 - Zebrafish/embryology
 - Zebrafish/genetics*
 - CCAAT-Enhancer-Binding Protein-delta
 - Gene Expression
 - Animals
 - Sequence Analysis, DNA
 - Zebrafish Proteins/genetics*
 - CCAAT-Enhancer-Binding Protein-beta/genetics
 - DNA, Complementary/chemistry
 - DNA, Complementary/genetics
 - DNA, Complementary/isolation & purification
 - CCAAT-Enhancer-Binding Proteins/genetics*
 - Transcription Factors*
 - Hematopoiesis/genetics
 - Gene Expression Regulation, Developmental
 
 - PubMed
 - 11750126 Full text @ Gene
 
            Citation
        
        
            Lyons, S.E., Shue, B.C., Lei, L., Oates, A.C., Zon, L.I., and Liu, P.P. (2001) Molecular cloning, genetic mapping, and expression analysis of four zebrafish c/ebp genes. Gene. 281(1-2):43-51.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The CCAAT/enhancer binding protein family (C/EBP) are transcription factors that play integral roles in the development and function of many organ systems, including hematopoietic cells, adipose tissues, and liver. We have identified and characterized putative zebrafish orthologs of mammalian C/EBP alpha, beta, gamma, and delta using low-stringency hybridization screening and computer searches of the GenBank EST database. c/ebpa and g were mapped within 1 cM of each other on linkage group (LG) 7, syntenic with human CEBPA and G genes on chromosome 19. c/ebpb was mapped to LG8, and c/ebpd was mapped to LG24, on the same LG as a recently identified unique c/ebp in zebrafish, c/ebp1. The mapping of these genes established new syntenic relationships between LG8 and human chromosome 20, extended existing synteny between LG7 and human chromosome 19, and confirmed the synteny between LG24 and human chromosome 8. In addition, these syntenies between zebrafish and human chromosomes are also conserved in the mouse genome. To characterize the expression of these genes, RNA in situ hybridization in embryos of wild type and a hematopoietic mutant, cloche, was performed. The results showed that zebrafish c/ebpa, b, g, and d were expressed in many embryonic tissues. c/ebpa and b were expressed in a subset of hematopoietic cells in a region consistent with myeloid expression. In addition, there was expression of c/ebpa and b in the liver and c/ebpa, b, and d in regions of the gastrointestinal tract. The expression of the c/ebps may serve as important markers for analysis of myelopoiesis, hepatic development, and other developmental processes in the future.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping