MeCP2 as an Activator of Gene Expression.

Abstract:

:Rett syndrome is a neurodevelopmental disorder that primarily affects females and is caused by mutations in the methyl-CpG-binding-protein 2 (MECP2) gene. Initially, MeCP2 had been shown to be a repressor of gene transcription. In their 2008 paper, Chahrour and colleagues (DOI: 10.1126/science.1153252) reported that MeCP2 could also function as a transcriptional activator.

journal_name

Trends Neurosci

journal_title

Trends in neurosciences

authors

Horvath PM,Monteggia LM

doi

10.1016/j.tins.2017.11.005

subject

Has Abstract

pub_date

2018-02-01 00:00:00

pages

72-74

issue

2

eissn

0166-2236

issn

1878-108X

pii

S0166-2236(17)30232-1

journal_volume

41

pub_type

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