PUBLICATION
            Left-Right Function of dmrt2 Genes Is Not Conserved between Zebrafish and Mouse
- Authors
- Lourenço, R., Lopes, S.S., and Saude, L.
- ID
- ZDB-PUB-110110-16
- Date
- 2010
- Source
- PLoS One 5(12): e14438 (Journal)
- Registered Authors
- Lopes, Susana, Lourenço, Raquel, Saude, Leonor
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Genotype
- In Situ Hybridization
- Cloning, Molecular
- Mesoderm/metabolism
- DNA-Binding Proteins/genetics*
- DNA-Binding Proteins/physiology
- Zebrafish
- Somites/metabolism
- Heterozygote
- Mice
- Species Specificity
- Transcription Factors/genetics*
- Transcription Factors/physiology
- Mice, Inbred C57BL
- Mutation
- Body Patterning
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/physiology
- Animals
 
- PubMed
- 21203428 Full text @ PLoS One
            Citation
        
        
            Lourenço, R., Lopes, S.S., and Saude, L. (2010) Left-Right Function of dmrt2 Genes Is Not Conserved between Zebrafish and Mouse. PLoS One. 5(12):e14438.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                BACKGROUND: Members of the Dmrt family, generally associated with sex determination, were shown to be involved in several other functions during embryonic development. Dmrt2 has been studied in the context of zebrafish development where, due to a duplication event, two paralog genes dmrt2a and dmrt2b are present. Both zebrafish dmrt2a/terra and dmrt2b are important to regulate left-right patterning in the lateral plate mesoderm. In addition, dmrt2a/terra is necessary for symmetric somite formation while dmrt2b regulates somite differentiation impacting on slow muscle development. One dmrt2 gene is also expressed in the mouse embryo, where it is necessary for somite differentiation but with an impact on axial skeleton development. However, nothing was known about its role during left-right patterning in the lateral plate mesoderm or in the symmetric synchronization of somite formation.
METHODOLOGY/PRINCIPAL FINDINGS: Using a dmrt2 mutant mouse line, we show that this gene is not involved in symmetric somite formation and does not regulate the laterality pathway that controls left-right asymmetric organ positioning. We reveal that dmrt2a/terra is present in the zebrafish laterality organ, the Kupffer's vesicle, while its homologue is excluded from the mouse equivalent structure, the node. On the basis of evolutionary sub-functionalization and neo-functionalization theories we discuss this absence of functional conservation.
CONCLUSIONS/SIGNIFICANCE: Our results show that the role of dmrt2 gene is not conserved during zebrafish and mouse embryonic development.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    