| Literature DB >> 11430798 |
Abstract
Methylation of genomic CpG residues is crucial for proper neuronal function. Rett syndrome, a common form of mental retardation, is associated with mutations in the gene encoding MeCP2, a methyl CpG binding protein linked to transcriptional repression. Gene knockouts of mouse Mecp2 have reproduced key aspects of the disease. A CNS-restricted knockout of Dnmt1, encoding the enzyme that maintains CpG methylation patterns, results in loss of mutant neurons and glia.Entities:
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Year: 2001 PMID: 11430798 DOI: 10.1016/s0896-6273(01)00325-7
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173