z-logo
Premium
In sickness and in health: the role of methyl‐CpG binding protein 2 in the central nervous system
Author(s) -
Díaz de LeónGuerrero Sol,
PedrazaAlva Gustavo,
PérezMartínez Leonor
Publication year - 2011
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2011.07658.x
Subject(s) - mecp2 , rett syndrome , epigenetics , neuroepithelial cell , biology , neuroscience , chromatin , central nervous system , regulation of gene expression , neurogenesis , microrna , repressor , genetics , gene , gene expression , embryonic stem cell , phenotype
The array of specialized neuronal and glial cell types that characterize the adult central nervous system originates from neuroepithelial proliferating precursor cells. The transition from proliferating neuroepithelial precursor cells to neuronal lineages is accompanied by rapid global changes in gene expression in coordination with epigenetic modifications at the level of the chromatin structure. A number of genetic studies have begun to reveal how epigenetic deregulation results in neurodevelopmental disorders such as mental retardation, autism, Rubinstein–Taybi syndrome and Rett syndrome. In this review we focus on the role of the methyl‐CpG binding protein 2 (MeCP2) during development of the central nervous system and its involvement in Rett syndrome. First, we present recent findings that indicate a previously unconsidered role of glial cells in the development of Rett syndrome. Next, we discuss evidence of how MeCP2 deficiency or loss of function results in aberrant gene expression leading to Rett syndrome. We also discuss MeCP2’s function as a repressor and activator of gene expression and the role of its different target genes, including microRNAs, during neuronal development. Finally, we address different signaling pathways that regulate MeCP2 expression at both the post‐transcriptional and post‐translational level, and discuss how mutations in MeCP2 may result in lack of responsiveness to environmental signals.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here