Imai Kenichi, Nakata Kenji, Kawai Kazuaki, Hamano Takaichi, Mei Nan, Kasai Hiroshi, Okamoto Takashi
Department of Molecular and Cellular Biology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601.
J Biol Chem. 2005 Jul 22;280(29):26701-13. doi: 10.1074/jbc.M503313200. Epub 2005 Jun 1.
To identify the cellular gene target for Tat, we performed gene expression profile analysis and found that Tat up-regulates the expression of the OGG1 (8-oxoguanine-DNA glycosylase-1) gene, which encodes an enzyme responsible for repairing the oxidatively damaged guanosine, 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxo-dG). We observed that Tat induced OGG1 gene expression by enhancing its promoter activity without changing its mRNA stability. We found that the upstream AP-4 site within the OGG1 promoter is responsible and that Tat interacted with AP-4 and removed AP-4 from the OGG1 promoter by in vivo chromatin immunoprecipitation assay. Thus, Tat appears to activate OGG1 expression by sequestrating AP-4. Interestingly, although Tat induces oxidative stress known to generate 8-oxo-dG, which causes the G:C to T:A transversion, we observed that the amount of 8-oxo-dG was reduced by Tat. When OGG1 was knocked down by small interfering RNA, Tat increased the amount of 8-oxo-dG, thus confirming the role of OGG1 in preventing the formation of 8-oxo-dG. These findings collectively indicate the possibility that Tat may play a role in maintenance of the genetic integrity of the proviral and host cellular genomes by up-regulating OGG1 as a feed-forward mechanism.
为了确定Tat的细胞基因靶点,我们进行了基因表达谱分析,发现Tat上调了OGG1(8-氧代鸟嘌呤-DNA糖基化酶-1)基因的表达,该基因编码一种负责修复氧化损伤的鸟苷8-氧代-7,8-二氢-2'-脱氧鸟苷(8-氧代-dG)的酶。我们观察到,Tat通过增强其启动子活性来诱导OGG1基因表达,而不改变其mRNA稳定性。我们发现OGG1启动子内的上游AP-4位点起作用,并且通过体内染色质免疫沉淀试验发现Tat与AP-4相互作用并将AP-4从OGG1启动子上移除。因此,Tat似乎通过隔离AP-4来激活OGG1表达。有趣的是,尽管Tat诱导已知会产生8-氧代-dG的氧化应激,而8-氧代-dG会导致G:C到T:A的颠换,但我们观察到Tat使8-氧代-dG的量减少。当用小干扰RNA敲低OGG1时,Tat增加了8-氧代-dG的量,从而证实了OGG1在防止8-氧代-dG形成中的作用。这些发现共同表明,Tat可能通过上调OGG1作为一种前馈机制,在维持原病毒和宿主细胞基因组的遗传完整性方面发挥作用。