PUBLICATION
            Conservation of sequence and expression of Xenopus and zebrafish dHAND during cardiac, branchial arch and lateral mesoderm development
- Authors
- Angelo, S., Lohr, J., Lee, K.H., Ticho, B.S., Breitbart, R.E., Hill, S., Yost, H.J., and Srivastava, D.
- ID
- ZDB-PUB-000824-16
- Date
- 2000
- Source
- Mechanisms of Development 95(1-2): 231-237 (Journal)
- Registered Authors
- Breitbart, Roger E., Ticho, Barry, Yost, H. Joseph
- Keywords
- dHAND; eHAND; Xenopus; zebrafish; heart; branchial arches; neural crest
- MeSH Terms
- 
    
        
        
            
                - Heart/embryology
- Heart/physiology
- Sequence Alignment
- Basic Helix-Loop-Helix Transcription Factors
- Zebrafish/embryology*
- Zebrafish/physiology*
- Humans
- Zebrafish Proteins
- Molecular Sequence Data
- Branchial Region/embryology
- Branchial Region/physiology
- Gene Expression Regulation, Developmental*
- Xenopus/embryology*
- Xenopus/physiology*
- Mice
- Xenopus Proteins
- Helix-Loop-Helix Motifs
- Animals
- Mesoderm/physiology
- Amino Acid Sequence
- DNA-Binding Proteins/physiology*
- Transcription Factors/physiology*
- Conserved Sequence
 
- PubMed
- 10906469 Full text @ Mech. Dev.
            Citation
        
        
            Angelo, S., Lohr, J., Lee, K.H., Ticho, B.S., Breitbart, R.E., Hill, S., Yost, H.J., and Srivastava, D. (2000) Conservation of sequence and expression of Xenopus and zebrafish dHAND during cardiac, branchial arch and lateral mesoderm development. Mechanisms of Development. 95(1-2):231-237.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                dHAND and eHAND are related basic helix-loop-helix transcription factors that are expressed in the cardiac mesoderm and in numerous neural crest-derived cell types in chick and mouse. To better understand the evolutionary development of overlapping expression and function of the HAND genes during embryogenesis, we cloned the zebrafish and Xenopus orthologues. Comparison of dHAND sequences in zebrafish, Xenopus, chick, mouse and human demonstrated conservation throughout the protein. Expression of dHAND in zebrafish was seen in the earliest precursors of all lateral mesoderm at early gastrulation stages. At neurula and later stages, dHAND expression was observed in lateral precardiac mesoderm, branchial arch neural crest derivatives and posterior lateral mesoderm. At looping heart stages, cardiac dHAND expression remained generalized with no apparent regionalization. Interestingly, no eHAND orthologue was found in zebrafish. In Xenopus, dHAND and eHAND were co-expressed in the cardiac mesoderm without the segmental restriction seen in mice. Xenopus dHAND and eHAND were also expressed bilaterally in the lateral mesoderm without any left-right asymmetry. Within the branchial arches, XdHAND was expressed in a broader domain than XeHAND, similar to their mouse counterparts. Together, these data demonstrate conservation of HAND structure and expression across species.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    