PUBLICATION
            Spatial and temporal expression patterns of Osbpl2a and Osbpl2b during zebrafish embryonic development
- Authors
 - Liu, C., Yao, J., Wei, Q., Xing, G., Cao, X.
 - ID
 - ZDB-PUB-160412-9
 - Date
 - 2016
 - Source
 - International journal of pediatric otorhinolaryngology 84: 174-9 (Journal)
 - Registered Authors
 - Keywords
 - Early development, Osbpl2a, Osbpl2b, Spatial and temporal expression, Zebrafish
 - MeSH Terms
 - 
    
        
        
            
                
- Genetic Markers
 - Zebrafish Proteins/genetics*
 - Zebrafish Proteins/metabolism
 - Amino Acid Sequence
 - Receptors, Steroid/genetics*
 - Receptors, Steroid/metabolism
 - Hearing Loss, Sensorineural/embryology*
 - Hearing Loss, Sensorineural/genetics
 - Hearing Loss, Sensorineural/metabolism
 - Female
 - Zebrafish
 - Molecular Sequence Data
 - In Situ Hybridization
 - Humans
 - Animals
 - Gene Expression Regulation, Developmental*
 
 - PubMed
 - 27063776 Full text @ Int. J. Pediatr. Otorhinolaryngol.
 
            Citation
        
        
            Liu, C., Yao, J., Wei, Q., Xing, G., Cao, X. (2016) Spatial and temporal expression patterns of Osbpl2a and Osbpl2b during zebrafish embryonic development. International journal of pediatric otorhinolaryngology. 84:174-9.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
Objective The mutated OSBPL2 (OMIM: 606731), encoding oxysterol binding protein-like protein 2, was recently identified as a novel causative gene for autosomal dominant nonsyndromic hearing loss (ADNSHL). We reported the expression patterns of Osbpl2 in zebrafish, in order to further understand the role of OSBPL2 in hearing formation and development.
Methods Zebrafish was used as an animal model, and the expression of Osbpl2 was investigated by whole mount in situ hybridization.
Results Bioinformatics analysis indicates that zebrafish has two homologues of Osbpl2 gene (Osbpl2a and Osbpl2b) and Osbpl2b is the orthologous gene of human OSBPL2. No expression of Osbpl2a and Osbpl2b mRNA is detected at 75% epiboly. The zygotical expression of the two genes has not been started at 11-somite stage. At 24h post-fertilization (hpf), both Osbpl2a and Osbpl2b are found at ventricle zone of brain, however, the expression level of Osbpl2a is higher than that of Osbpl2b. When embryos are 48hpf, the expression level of Osbpl2a and Osbpl2b becomes higher at the ventricle zone. At 72hpf, Osbpl2b is only found at liver primordium, while Osbpl2a is not detected anywhere obviously. At 96hpf, Osbpl2b is found at pharyngeal arches, liver, digestive tract and otic vesicle, while Osbpl2a remains undetected.
Conclusion Osbpl2b was demonstrated to be the orthologous gene of human OSBPL2, which has strong maternal expression, while Osbpl2a was detected without obvious maternal expression. This work would contribute to the further study of the molecular mechanism and function of OSBPL2 implicated with ADNSHL.
            
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping