| Literature DB >> 20056891 |
Ian Maze1, Herbert E Covington, David M Dietz, Quincey LaPlant, William Renthal, Scott J Russo, Max Mechanic, Ezekiell Mouzon, Rachael L Neve, Stephen J Haggarty, Yanhua Ren, Srihari C Sampath, Yasmin L Hurd, Paul Greengard, Alexander Tarakhovsky, Anne Schaefer, Eric J Nestler.
Abstract
Cocaine-induced alterations in gene expression cause changes in neuronal morphology and behavior that may underlie cocaine addiction. In mice, we identified an essential role for histone 3 lysine 9 (H3K9) dimethylation and the lysine dimethyltransferase G9a in cocaine-induced structural and behavioral plasticity. Repeated cocaine administration reduced global levels of H3K9 dimethylation in the nucleus accumbens. This reduction in histone methylation was mediated through the repression of G9a in this brain region, which was regulated by the cocaine-induced transcription factor DeltaFosB. Using conditional mutagenesis and viral-mediated gene transfer, we found that G9a down-regulation increased the dendritic spine plasticity of nucleus accumbens neurons and enhanced the preference for cocaine, thereby establishing a crucial role for histone methylation in the long-term actions of cocaine.Entities:
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Year: 2010 PMID: 20056891 PMCID: PMC2820240 DOI: 10.1126/science.1179438
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728