3.8 Article

A transcriptional repressor MeCP2 causing Rett syndrome is expressed in embryonic non-neuronal cells and controls their growth

Journal

DEVELOPMENTAL BRAIN RESEARCH
Volume 157, Issue 1, Pages 103-106

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.devbrainres.2005.03.011

Keywords

astrocyte; MeCP2; DNA methylation; epigenetic; Rett syndrome; microcephaly

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An epigenetic key protein MeCP2 is thought to be expressed exclusively in mature neurons. Here, we show that MeCP2 is expressed in embryonic non-neuronal cells by immunocytochemistry and Western blotting, and that knockdown of McCP2 levels using RNA interference reduces their proliferation. These findings suggest that MeCP2 is essential to non-neuronal cell growth during brain development, which may be associated with microcephaly of Rett syndrome patients with MeCP2 mutations. (c) 2005 Elsevier B.V All rights reserved.

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