Over Expression Of Wild Type Or A Catalytically Dead Mutant Of Sirtuin 6 Does Not Influence Nf Kappa B Responses

SIRT6 is involved in inflammation, aging and metabolism potentially by modulating the functions of both NF kappa B and HIF1 alpha. Since it is possible to make small molecule activators and inhibitors of Sirtuins we wished to establish biochemical and cellular assays both to assist in drug discovery efforts and to validate whether SIRT6 represents a valid drug target for these indications. We confirmed in cellular assays that SIRT6 can deacetylate acetylated-histone H3 lysine 9 (H3K9Ac), however this deacetylase activity is unusually low in biochemical assays. In an effort to develop alternative assay formats we observed that SIRT6 overexpression had no influence on TNF alpha induced nuclear translocation of NFkB, nor did it have an effect on nuclear mobility of RelA/p65. In an effort to identify a gene expression profile that could be used to identify a SIRT6 readout we conducted genome-wide expression studies. We observed that overexpression of SIRT6 had little influence on NF kappa B-dependent genes, but overexpression of the catalytically inactive mutant affected gene expression in developmental pathways.