Guha Prajna, Aneja Kawalpreet K, Shilpi Rasheda Y, Haldar Dipak
Department of Biological Sciences, St. John's University, Queens, NY 11439, USA.
Arch Biochem Biophys. 2009 Oct 15;490(2):85-95. doi: 10.1016/j.abb.2009.07.027. Epub 2009 Aug 13.
We have recently identified two promoters, distal and proximal for rat mitochondrial glycerophosphate acyltransferase (mtGPAT). Here we are reporting further characterization of the promoters. Insulin and epidermal growth factor (EGF) stimulated while leptin and glucagon inhibited the luciferase activity of the distal promoter and the amounts of the distal transcript. Conversely, luciferase activity of the proximal promoter and proximal transcript remained unchanged due to these treatments. Only the distal promoter has binding sites for carbohydrate response element binding protein (ChREBP) and sterol regulatory element binding protein-1 (SREBP-1). Electromobility shift assays and chromatin immunoprecipitation assays demonstrated that ChREBP and SREBP-1 bind to the mtGPAT distal promoter. Insulin and EGF increased while glucagon and leptin decreased the binding of SREBP-1 and ChREBP to the distal promoter. Thus, the distal promoter is the regulatory promoter while the proximal promoter acts constitutively for rat mtGPAT gene under the influence of hormones and growth factor.
我们最近鉴定出大鼠线粒体甘油磷酸酰基转移酶(mtGPAT)的两个启动子,分别为远端启动子和近端启动子。在此,我们报告这些启动子的进一步特征。胰岛素和表皮生长因子(EGF)可刺激远端启动子的荧光素酶活性以及远端转录本的量,而瘦素和胰高血糖素则抑制它们。相反,近端启动子的荧光素酶活性和近端转录本的量在这些处理后保持不变。只有远端启动子具有碳水化合物反应元件结合蛋白(ChREBP)和固醇调节元件结合蛋白-1(SREBP-1)的结合位点。电泳迁移率变动分析和染色质免疫沉淀分析表明,ChREBP和SREBP-1可结合至mtGPAT远端启动子。胰岛素和EGF增加了SREBP-1和ChREBP与远端启动子的结合,而胰高血糖素和瘦素则减少了这种结合。因此,在激素和生长因子的影响下,远端启动子是调节性启动子,而近端启动子则持续作用于大鼠mtGPAT基因。