Suppr超能文献

脂肪酸合酶启动子中胰岛素反应元件的鉴定。

Identification of an insulin response element in the fatty acid synthase promoter.

作者信息

Moustaïd N, Beyer R S, Sul H S

机构信息

Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts 02115.

出版信息

J Biol Chem. 1994 Feb 25;269(8):5629-34.

PMID:8119899
Abstract

We have previously reported that insulin increases fatty acid synthase (FAS) gene transcription, and that sequences responsible for positive regulation are located within the first 332 base pairs of the FAS promoter. To define minimal sequences required for insulin regulation within this region, chimeric constructs containing serial 5' deletions starting at -318 and extending through position +67 of the rat FAS gene ligated to the luciferase reporter gene were transfected into 3T3-L1 adipocytes. Insulin treatment at 10 nM increased luciferase activity 2-3-fold in 3T3-L1 adipocytes transfected with constructs containing progressive deletions from -318 to -67. This stimulation of the FAS promoter activity by insulin was dose-dependent. However, no effect of insulin was observed when fusion constructs containing FAS promoter sequences spanning from -25 or from -19 to +67 were transfected into adipocytes. These results suggest that the insulin response sequences of the FAS gene may be located in the region from -67 to -25. DNase I footprinting using liver nuclear extracts revealed a protected region spanning -71 and -50 in addition to a region near the putative TATA box. Gel mobility shift assays using the sequence from -71 to -50 as a probe revealed nuclear factor(s) from mouse liver and 3T3-L1 adipocytes that specifically complexed with this sequence. Mutational analysis of this region showed that sequences between -68 and -60 are essential for recognition and interaction with a trans-acting factor(s). Moreover, when three tandem repeats of the sequences spanning -68 to -52 were linked to the SV40 promoter and used for transfection, luciferase activity increased 3.6-fold in response to insulin treatment. Thus, we have identified novel cis-acting DNA sequences responsible for insulin regulation of the FAS gene, which interact with nuclear protein(s) from liver and adipocytes and which are found to share limited homology to insulin response sequences present in other genes.

摘要

我们之前曾报道,胰岛素可增加脂肪酸合酶(FAS)基因的转录,且负责正向调控的序列位于FAS启动子的前332个碱基对之内。为了确定该区域内胰岛素调控所需的最小序列,将包含从大鼠FAS基因-318开始并延伸至+67位置的连续5'端缺失的嵌合构建体与荧光素酶报告基因连接后,转染至3T3-L1脂肪细胞中。在用包含从-318到-67逐步缺失的构建体转染的3T3-L1脂肪细胞中,10 nM胰岛素处理使荧光素酶活性增加了2至3倍。胰岛素对FAS启动子活性的这种刺激是剂量依赖性的。然而,当将包含从-25或从-19到+67的FAS启动子序列的融合构建体转染至脂肪细胞中时,未观察到胰岛素的作用。这些结果表明,FAS基因的胰岛素反应序列可能位于-67至-25区域。使用肝核提取物进行的DNase I足迹分析显示,除了推定的TATA框附近的区域外,还有一个跨越-71至-50的受保护区域。使用从-71至-50的序列作为探针进行的凝胶迁移率变动分析显示,来自小鼠肝脏和3T3-L1脂肪细胞的核因子与该序列特异性结合。对该区域的突变分析表明,-68至-60之间的序列对于与反式作用因子的识别和相互作用至关重要。此外,当将跨越-68至-52的序列的三个串联重复与SV40启动子连接并用于转染时,胰岛素处理后荧光素酶活性增加了3.6倍。因此,我们鉴定出了负责FAS基因胰岛素调控的新型顺式作用DNA序列,它们与肝脏和脂肪细胞中的核蛋白相互作用,并且发现与其他基因中存在的胰岛素反应序列具有有限的同源性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验