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Publication : SIRT1-mediated deacetylation of MeCP2 contributes to BDNF expression.

First Author  Zocchi L Year  2012
Journal  Epigenetics Volume  7
Issue  7 Pages  695-700
PubMed ID  22677942 Mgi Jnum  J:323994
Mgi Id  MGI:7264825 Doi  10.4161/epi.20733
Citation  Zocchi L, et al. (2012) SIRT1-mediated deacetylation of MeCP2 contributes to BDNF expression. Epigenetics 7(7):695-700
abstractText  Methyl-CpG binding protein 2 (MeCP2) binds methylated cytosines at CpG sites on DNA and it is thought to function as a critical epigenetic regulator. Mutations in the MeCP2 gene have been associated to Rett syndrome, a human neurodevelopmental disorder. Here we show that MeCP2 is acetylated by p300 and that SIRT1 mediates its deacetylation. SIRT1, the mammalian homologue of Sir2 in yeast, is a nicotinamide-adenine dinucleotide (NAD(+))-dependent histone deacetylase that belongs to the family of HDAC class III sirtuins. Importantly, SIRT1 has been shown to play a critical role in synaptic plasticity and memory formation. This study reveals a functional interplay between two critical epigenetic regulators, MeCP2 and SIRT1, which controls MeCP2 binding activity to the brain-derived neurotrophic factor (BDNF) promoter in a specific region of the brain.
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