Literature DB >> 21081649

SIRT2 regulates NF-κB dependent gene expression through deacetylation of p65 Lys310.

Karin M Rothgiesser1, Süheda Erener, Susanne Waibel, Bernhard Lüscher, Michael O Hottiger.   

Abstract

NF-κB regulates the expression of a large number of target genes involved in the immune and inflammatory response, apoptosis, cell proliferation, differentiation and survival. In this study, we identified SIRT2 as a deacetylase of the transcription factor p65. SIRT2 is a member of the family of sirtuins, which are NAD(+)-dependent deacetylases involved in several cellular processes. SIRT2 interacts with p65 in the cytoplasm and deacetylates p65 in vitro and in vivo at Lys310. Moreover, p65 is hyperacetylated at Lys310 in Sirt2(-/-) cells after TNFα stimulation, which results in the increase in expression of a subset of p65 acetylation-dependent target genes. Our work provides evidence that p65 is deacetylated by SIRT2 in the cytoplasm to regulate the expression of specific NF-κB-dependent genes.

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Year:  2010        PMID: 21081649     DOI: 10.1242/jcs.073783

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  144 in total

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Journal:  Hum Mol Genet       Date:  2014-01-16       Impact factor: 6.150

7.  Specific ablation of Nampt in adult neural stem cells recapitulates their functional defects during aging.

Authors:  Liana R Stein; Shin-ichiro Imai
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8.  The interaction between acetylation and serine-574 phosphorylation regulates the apoptotic function of FOXO3.

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9.  Sirtuin 2-mediated deacetylation of cyclin-dependent kinase 9 promotes STAT1 signaling in type I interferon responses.

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Journal:  J Biol Chem       Date:  2018-11-28       Impact factor: 5.157

10.  SIRT2-Mediated Deacetylation and Tetramerization of Pyruvate Kinase Directs Glycolysis and Tumor Growth.

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Journal:  Cancer Res       Date:  2016-04-27       Impact factor: 12.701

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