Institute of Veterinary Biochemistry and Molecular Biology, University of Zurich, Winterthurerstraße 190, 8057 Zurich, Switzerland.
J Cell Sci. 2010 Dec 15;123(Pt 24):4251-8. doi: 10.1242/jcs.073783. Epub 2010 Nov 16.
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.
NF-κB 调节大量参与免疫和炎症反应、细胞凋亡、细胞增殖、分化和存活的靶基因的表达。在这项研究中,我们鉴定出 SIRT2 是转录因子 p65 的去乙酰化酶。SIRT2 是 sirtuins 家族的一员,该家族是 NAD(+)依赖性去乙酰化酶,参与多种细胞过程。SIRT2 在细胞质中与 p65 相互作用,并在体外和体内将 p65 赖氨酸 310 去乙酰化。此外,在 TNFα 刺激后,Sirt2(-/-)细胞中的 p65 在赖氨酸 310 处过度乙酰化,导致一组依赖于 p65 乙酰化的靶基因的表达增加。我们的工作提供了证据,表明 p65 在细胞质中被 SIRT2 去乙酰化,以调节特定的 NF-κB 依赖性基因的表达。