Maehara Kayoko, Uekawa Natsuko, Isobe Ken-Ichi
Department of Basic Gerontology, National Institute for Longevity Sciences, 36-3 Gengo, Morioka-cho, Obu, Aichi 474-8522, Japan.
Biochem Biophys Res Commun. 2002 Jul 5;295(1):187-92. doi: 10.1016/S0006-291X(02)00646-0.
To better understand the link between chromatin modification and manganese superoxide dismutase (Mn-SOD) gene expression, we have investigated the level of histone acetylation at Mn-SOD proximal promoter. TSA induced the expression of Mn-SOD mRNA and its transcriptional activity in C2C12 cells. Sp1 binding sites in the proximal promoter region of Mn-SOD were transcriptionally responsive to TSA by transfection studies. We have detected a localized acetylation of histones H3 and H4, in vivo occupation by Sp1, early growth responsive-1 (Egr-1), and histone deacetylase-1 (HDAC1) in the proximal promoter region of Mn-SOD gene using chromatin immunoprecipitation assays. Our findings indicate that Mn-SOD gene expression is repressed by Sp1-HDAC1 complex. This repression is released by a localized histone acetylation and at least in parts a displacement by Egr-1 in response to TSA.
为了更好地理解染色质修饰与锰超氧化物歧化酶(Mn-SOD)基因表达之间的联系,我们研究了Mn-SOD近端启动子处组蛋白乙酰化水平。曲古抑菌素A(TSA)诱导了C2C12细胞中Mn-SOD mRNA的表达及其转录活性。通过转染研究发现,Mn-SOD近端启动子区域的Sp1结合位点对TSA具有转录反应性。我们使用染色质免疫沉淀试验检测到Mn-SOD基因近端启动子区域组蛋白H3和H4的局部乙酰化、Sp1、早期生长反应因子-1(Egr-1)和组蛋白去乙酰化酶-1(HDAC1)在体内的占据情况。我们的研究结果表明,Mn-SOD基因表达受到Sp1-HDAC1复合物的抑制。这种抑制通过局部组蛋白乙酰化以及至少部分地通过Egr-1响应TSA的取代作用而解除。