Document Detail


Evolving role of MeCP2 in Rett syndrome and autism.
MedLine Citation:
PMID:  20473347     Owner:  NLM     Status:  In-Process    
Abstract/OtherAbstract:
Rett syndrome is an X-linked autism-spectrum disorder caused by mutations in MECP2, encoding methyl CpG-binding protein 2. Since the discovery of MECP2 mutations as the genetic cause of Rett syndrome, the understanding of MeCP2 function has evolved. Although MeCP2 was predicted to be a global transcriptional repressor of methylated promoters, large-scale combined epigenomic approaches of MeCP2 binding, methylation and gene expression have demonstrated that MeCP2 binds preferentially to intergenic and intronic regions, and sparsely methylated promoters of active genes. This review compares the evolution of thought within two ‘classic’ epigenetic mechanisms of parental imprinting and X chromosome inactivation to that of the MeCP2 field, and considers the future relevance of integrated epigenomic databases to understanding autism and Rett syndrome.
Authors:
Janine M LaSalle; Dag H Yasui
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Epigenomics     Volume:  1     ISSN:  1750-192X     ISO Abbreviation:  Epigenomics     Publication Date:  2009 Oct 
Date Detail:
Created Date:  2012-03-15     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101519720     Medline TA:  Epigenomics     Country:  England    
Other Details:
Languages:  eng     Pagination:  119-30     Citation Subset:  IM    
Affiliation:
Medical Microbiology and Immunology and Rowe Program in Human Genetics, University of California Davis School of Medicine, Davis, CA 95616, USA. jmlasalle@ucdavis.edu
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