PUBLICATION
            5-hydroxymethylcytosine marks post-mitotic neural cells in the adult and developing vertebrate central nervous system
- Authors
- Diotel, N., Mérot, Y., Coumailleau, P., Gueguen, M.M., Sérandour, A.A., Salbert, G., Kah, O.
- ID
- ZDB-PUB-160716-16
- Date
- 2017
- Source
- The Journal of comparative neurology 525(3): 478-497 (Journal)
- Registered Authors
- Diotel, Nicolas, Kah, Olivier
- Keywords
- Key words: 5mC, 5hmC, MeCP2, TET, amphibian, epigenetic, mammals, neurogenesis, teleost
- MeSH Terms
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                - Immunohistochemistry
- Zebrafish
- Real-Time Polymerase Chain Reaction
- Dermoscopy
- Animals, Genetically Modified
- Neurogenesis/physiology
- Neural Stem Cells/cytology
- Neural Stem Cells/metabolism
- Neuroglia/cytology
- Neuroglia/metabolism
- Animals
- Brain/cytology
- Brain/growth & development*
- Brain/metabolism*
- Xenopus
- 5-Methylcytosine/analogs & derivatives*
- 5-Methylcytosine/metabolism
- Male
- Microscopy, Confocal
- Neurons/cytology
- Neurons/metabolism*
- Olfactory Mucosa/cytology
- Olfactory Mucosa/growth & development
- Olfactory Mucosa/metabolism
- In Situ Hybridization
- Green Fluorescent Proteins/genetics
- Green Fluorescent Proteins/metabolism
- Mice
 
- PubMed
- 27414756 Full text @ J. Comp. Neurol.
            Citation
        
        
            Diotel, N., Mérot, Y., Coumailleau, P., Gueguen, M.M., Sérandour, A.A., Salbert, G., Kah, O. (2017) 5-hydroxymethylcytosine marks post-mitotic neural cells in the adult and developing vertebrate central nervous system. The Journal of comparative neurology. 525(3):478-497.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The epigenetic mark 5-hydroxymethylcytosine (5hmC) is a cytosine modification that is abundant in the central nervous system of mammals and which results from 5-methylcytosine oxidation by TET enzymes. Such a mark is suggested to play key roles in the regulation of chromatin structure and gene expression. However, its precise functions still remain poorly understood and information about its distribution in non-mammalian species is still lacking. Here, the distribution of 5hmC was investigated in the brain of adult zebrafish, African claw frog and mouse in a comparative manner. We show that zebrafish neurons are endowed with high levels of 5hmC whereas quiescent or proliferative neural progenitors show low to undetectable levels of the modified cytosine. In the brain of larval and juvenile xenopus, 5hmC is also detected in neurons while ventricular proliferative cells do not display this epigenetic mark. Similarly, 5hmC is enriched in neurons compared to neural progenitors of the ventricular zone in the mouse developing cortex. Interestingly, 5hmC colocalized with the methylated DNA binding protein MeCP2 and with the active chromatin histone modification H3K4me2 in mouse neurons. Taken together, our results show an evolutionarily conserved cerebral distribution of 5hmC between fish and tetrapods and reinforce the idea that 5hmC fulfills major functions in the control of chromatin activity in vertebrate neurons.
            
    
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    