PUBLICATION
            Expression of patched, prdm1 and engrailed in the lamprey somite reveals conserved responses to Hedgehog signaling
- Authors
 - Hammond, K.L., Baxendale, S., McCauley, D.W., Ingham, P.W., and Whitfield, T.T.
 - ID
 - ZDB-PUB-090217-7
 - Date
 - 2009
 - Source
 - Evolution & development 11(1): 27-40 (Journal)
 - Registered Authors
 - Baxendale, Sarah, Hammond, Katherine L., Ingham, Philip, Whitfield, Tanya T.
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Cluster Analysis
 - DNA, Complementary/genetics
 - Animals
 - Muscle, Skeletal/embryology
 - Muscle, Skeletal/metabolism
 - Base Sequence
 - Phylogeny
 - Receptors, Cell Surface/genetics
 - Receptors, Cell Surface/metabolism
 - In Situ Hybridization
 - Lampreys/embryology*
 - Lampreys/metabolism
 - Signal Transduction/genetics*
 - Sequence Analysis, DNA
 - Somites/anatomy & histology
 - Somites/metabolism*
 - Molecular Sequence Data
 - Genes, Developmental/genetics*
 - Hedgehog Proteins/metabolism*
 - Gene Expression Regulation, Developmental/genetics*
 
 - PubMed
 - 19196331 Full text @ Evol. Dev.
 
            Citation
        
        
            Hammond, K.L., Baxendale, S., McCauley, D.W., Ingham, P.W., and Whitfield, T.T. (2009) Expression of patched, prdm1 and engrailed in the lamprey somite reveals conserved responses to Hedgehog signaling. Evolution & development. 11(1):27-40.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                In the zebrafish embryo, expression of the prdm1 and patched1 genes in adaxial cells is indicative of their specification to give rise to slow twitch muscle fibers in response to Hedgehog (Hh) signaling. Subsets of these slow twitch muscle progenitors activate engrailed (eng) strongly in response to high-level Hh signaling, and differentiate into muscle pioneer cells, which are important for subsequent development of the horizontal myoseptum. In addition, eng is expressed more weakly in medial fast fibers in response to lower Hh levels. Somite morphology in the lamprey, an agnathan (jawless) vertebrate, differs significantly from that of teleosts. In particular, the lamprey does not have clear epaxial/hypaxial domains, lacks a horizontal myoseptum, and does not appear to possess distinct populations of fast and slow fibers in the embryonic somite. Nevertheless, Hh is expressed in the midline of the lamprey embryo, and we report here that, as in zebrafish, homologues of patched and prdm1 are expressed in adaxial regions of the lamprey somite, and an eng homologue is also expressed in the somite. However, the lamprey adaxial region does not exhibit the same distinct adaxial cell morphology as in the zebrafish. In addition, the expression of follistatin is not excluded from the adaxial region, and eng is not detected in discrete muscle pioneer-like cells. These data suggest the presence of conserved responses to Hh signaling in lamprey somites, although the full range of effects elicited by Hh in the zebrafish somite is not recapitulated.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping