PUBLICATION
            Histone deacetylase 1 (HDAC-1) required for the normal formation of craniofacial cartilage and pectoral fins of the zebrafish
- Authors
 - Pillai, R., Coverdale, L.E., Dubey, G., and Martin, C.C.
 - ID
 - ZDB-PUB-040920-6
 - Date
 - 2004
 - Source
 - Developmental Dynamics : an official publication of the American Association of Anatomists 231(3): 647-654 (Journal)
 - Registered Authors
 - Martin, C. Cristofre
 - Keywords
 - histone deacetylase, cartilage, fin bud, heart, morpholino, insertional mutant, zebrafish
 - MeSH Terms
 - 
    
        
        
            
                
- Embryo, Mammalian/drug effects
 - Oligonucleotides, Antisense/pharmacology
 - Histone Deacetylases/metabolism
 - Histone Deacetylases/physiology*
 - Alcian Blue/metabolism
 - Animals
 - Zebrafish Proteins/metabolism
 - Zebrafish Proteins/physiology*
 - Embryo, Nonmammalian
 - Mutagenesis, Insertional
 - Skull/embryology*
 - Embryonic Development
 - Homozygote
 - Cartilage/embryology*
 - Time Factors
 - In Situ Hybridization
 - Histone Deacetylase 1
 - Extremities/embryology*
 - Zebrafish/embryology*
 - Gene Expression Regulation, Developmental
 
 - PubMed
 - 15376317 Full text @ Dev. Dyn.
 
            Citation
        
        
            Pillai, R., Coverdale, L.E., Dubey, G., and Martin, C.C. (2004) Histone deacetylase 1 (HDAC-1) required for the normal formation of craniofacial cartilage and pectoral fins of the zebrafish. Developmental Dynamics : an official publication of the American Association of Anatomists. 231(3):647-654.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Histone deacetylases interact with nucleosomes to facilitate the formation of transcriptionally repressed chromatin. In the present study, we show that histone deacetylase 1 (hdac-1) is expressed throughout embryonic development of the zebrafish. The expression of hdac-1 is ubiquitous in early embryos (2-16 hr postfertilization), but at later stages (36 and 48 hr postfertilization), it is primarily restricted to the branchial arches, fin bud mesenchyme, and hindbrain. We report the phenotypes of hdac-1 homozygous mutant embryos and embryos injected with an hdac-1 antisense morpholino. These embryos possess a complex phenotype affecting several embryonic structures. We observed developmental abnormalities in the heart and neural epithelial structures, including the retina and the loss of craniofacial cartilage and pectoral fins. Developmental Dynamics, 2004. Copyright 2004 Wiley-Liss, Inc.
            
    
        
        
    
    
    
                
                    
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