PUBLICATION
            Induced formation of primordial germ cells from zebrafish blastomeres by germplasm factors
- Authors
 - Wang, X., Zhu, J., Wang, H., Deng, W., Jiao, S., Wang, Y., He, M., Zhang, F., Liu, T., Hao, Y., Ye, D., Sun, Y.
 - ID
 - ZDB-PUB-231215-11
 - Date
 - 2023
 - Source
 - Nature communications 14: 79187918 (Journal)
 - Registered Authors
 - He, Mudan, Sun, Yonghua, Ye, Ding
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Blastula
 - Animals
 - Zebrafish*/genetics
 - Male
 - Germ Cells
 - Blastomeres*
 
 - PubMed
 - 38097571 Full text @ Nat. Commun.
 
            Citation
        
        
            Wang, X., Zhu, J., Wang, H., Deng, W., Jiao, S., Wang, Y., He, M., Zhang, F., Liu, T., Hao, Y., Ye, D., Sun, Y. (2023) Induced formation of primordial germ cells from zebrafish blastomeres by germplasm factors. Nature communications. 14:79187918.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The combination of genome editing and primordial germ cell (PGC) transplantation has enormous significance in the study of developmental biology and genetic breeding, despite its low efficiency due to limited number of donor PGCs. Here, we employ a combination of germplasm factors to convert blastoderm cells into induced PGCs (iPGCs) in zebrafish and obtain functional gametes either through iPGC transplantation or via the single blastomere overexpression of germplasm factors. Zebrafish-derived germplasm factors convert blastula cells of Gobiocypris rarus into iPGCs, and Gobiocypris rarus spermatozoa can be produced by iPGC-transplanted zebrafish. Moreover, the combination of genome knock-in and iPGC transplantation perfectly resolves the contradiction between high knock-in efficiency and early lethality during embryonic stages and greatly improves the efficiency of genome knock-in. Together, we present an efficient method for generating PGCs in a teleost, a technique that will have a strong impact in basic research and aquaculture.
            
    
        
        
    
    
    
                
                    
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