PUBLICATION
            Cloning and expression pattern of the lysozyme C gene in zebrafish
- Authors
- Liu, F. and Wen, Z.
- ID
- ZDB-PUB-020402-6
- Date
- 2002
- Source
- Mechanisms of Development 113(1): 69-72 (Journal)
- Registered Authors
- Liu, Feng, Wen, Zilong
- Keywords
- zebrafish; lysozyme C; L-plastin; PU.1; macrophage; yolksac; inter-mediate cell mass; kidney; hematopoiesis
- MeSH Terms
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                - Reverse Transcriptase Polymerase Chain Reaction
- Gene Expression Regulation, Developmental
- Tissue Distribution
- Muramidase/biosynthesis*
- Muramidase/genetics*
- Time Factors
- Zebrafish
- Blotting, Southern
- Blotting, Northern
- In Situ Hybridization
- Cloning, Molecular
- DNA, Complementary/metabolism
- Zebrafish Proteins/biosynthesis*
- Zebrafish Proteins/genetics*
- Amino Acid Sequence
- Molecular Sequence Data
- Animals
- Base Sequence
 
- PubMed
- 11900976 Full text @ Mech. Dev.
            Citation
        
        
            Liu, F. and Wen, Z. (2002) Cloning and expression pattern of the lysozyme C gene in zebrafish. Mechanisms of Development. 113(1):69-72.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Here, we report isolation and developmental expression pattern of the zebrafish lysozyme C gene. Amino acid sequence analysis showed that the zebrafish lysozyme C protein shared approximately 37-80% identities with the mouse, human, chicken, and carp counterparts. Whole-mount in situ hybridization showed that the lysozyme C gene was expressed in macrophages, as its expression was co-localized with the known myeloid lineage markers L-plastin and PU.1. At 20 hours postfertilization (hpf), most of the lysozyme C positive cells were localized in the yolksac and head mesenchyme but not in the intermediate cell mass, supporting the notion that the primitive macrophage originated from the yolksac (Development 126 (1999) 3735). At 36hpf, the lysozyme C positive cells scattered within the head and yolksac, and began to appear in the caudal part of axial vein. By 6 days postfertilization (dpf), the lysozyme C positive cells accumulated in the kidney where hematopoiesis had been indicated to take place after 4dpf (Dev. Dyn. 214 (1999) 323). Taken together, our results demonstrate that the lysozyme C gene is specifically expressed in myeloid lineage, suggesting that it could serve as an excellent marker for genetic screening of both primitive and definitive myeloid lineage development in zebrafish.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    