Reading the unique DNA methylation landscape of the brain: Non-CpG methylation, hydroxymethylation, and MeCP2.

Abstract:

:DNA methylation at CpG dinucleotides is an important epigenetic regulator common to virtually all mammalian cell types, but recent evidence indicates that during early postnatal development neuronal genomes also accumulate uniquely high levels of two alternative forms of methylation, non-CpG methylation and hydroxymethylation. Here we discuss the distinct landscape of DNA methylation in neurons, how it is established, and how it might affect the binding and function of protein readers of DNA methylation. We review studies of one critical reader of DNA methylation in the brain, the Rett syndrome protein methyl CpG-binding protein 2 (MeCP2), and discuss how differential binding affinity of MeCP2 for non-CpG and hydroxymethylation may affect the function of this methyl-binding protein in the nervous system.

authors

Kinde B,Gabel HW,Gilbert CS,Griffith EC,Greenberg ME

doi

10.1073/pnas.1411269112

subject

Has Abstract

pub_date

2015-06-02 00:00:00

pages

6800-6

issue

22

eissn

0027-8424

issn

1091-6490

pii

1411269112

journal_volume

112

pub_type

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