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KAP1-mediated epigenetic repression in the forebrain modulates behavioral vulnerability to stress.

Abstract : KAP1 is an essential cofactor of KRAB-zinc finger proteins, a family of vertebrate-specific epigenetic repressors of largely unknown functions encoded in the hundreds by the mouse and human genomes. Here, we report that KAP1 is expressed at high levels and necessary for KRAB-mediated repression in mature neurons of the mouse brain. Mice deleted for KAP1 in the adult forebrain exhibit heightened levels of anxiety-like and exploratory activity and stress-induced alterations in spatial learning and memory. In the hippocampus, a small number of genes are dysregulated, including some imprinted genes. Chromatin analyses of the promoters of two genes markedly upregulated in knockout mice reveal decreased histone 3 K9-trimethylation and increased histone 3 and histone 4 acetylation. We propose a model in which the tethering of KAP1-associated chromatin remodeling factors via KRAB-ZFPs epigenetically controls gene expression in the hippocampus, thereby conditioning responses to behavioral stress.
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https://www.hal.inserm.fr/inserm-00350884
Contributor : Maité Peney <>
Submitted on : Wednesday, January 7, 2009 - 5:05:12 PM
Last modification on : Thursday, April 23, 2020 - 2:26:26 PM

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Johan Jakobsson, Maria Isabel Cordero, Reto Bisaz, Anna Groner, Volker Busskamp, et al.. KAP1-mediated epigenetic repression in the forebrain modulates behavioral vulnerability to stress.. Neuron, Elsevier, 2008, 60 (5), pp.818-31. ⟨10.1016/j.neuron.2008.09.036⟩. ⟨inserm-00350884⟩

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