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负责饮食诱导的大鼠脂肪酸合酶(FAS)调节的三方DNA元件。

The tripartite DNA element responsible for diet-induced rat fatty acid synthase (FAS) regulation.

作者信息

Roder K, Klein H, Kranz H, Beck K F, Schweizer M

机构信息

Institut für Mikrobiologie und Biochemie, Universität Erlangen-Nürnberg, Germany.

出版信息

Gene. 1994 Jul 8;144(2):189-95. doi: 10.1016/0378-1119(94)90377-8.

Abstract

We investigated which region of the 5'-flanking sequence of the rat fatty acid synthase (FAS)-encoding gene could be responsible for its nutritionally regulated expression. Diet-induced differences in chromatin structure were determined by DNase I treatment of intact nuclei from hepatic tissue. A low-fat diet results in a different pattern of DNase I-hypersensitive sites (HS) in the chromatin of the FAS promoter (pFAS) from that seen when the nuclear extract was prepared from the livers of normally fed rats. The protein-binding properties of the region defined by DNase I hypersensitivity were tested by gel retardation. A putative cis-acting element with a tripartite structure, 5'-GCCT, 6-bp spacer and a 3'-palindrome, could be localized between bp -518 to -495 in pFAS. Competition experiments with oligodeoxyribonucleotides (oligos) representing subfragments of this cis-element showed that the requirement for structure is stricter than that for sequence. This element could be one of the termini of the insulin-induced signal cascade.

摘要

我们研究了大鼠脂肪酸合酶(FAS)编码基因5'-侧翼序列的哪个区域可能负责其营养调控表达。通过对肝组织完整细胞核进行DNase I处理来确定饮食诱导的染色质结构差异。低脂饮食导致FAS启动子(pFAS)染色质中DNase I超敏位点(HS)的模式与从正常喂养大鼠肝脏制备核提取物时所见不同。通过凝胶阻滞试验检测了由DNase I超敏性定义区域的蛋白质结合特性。一个具有三方结构(5'-GCCT、6个碱基对的间隔区和3'-回文序列)的假定顺式作用元件可定位于pFAS中-518至-495碱基对之间。用代表该顺式元件亚片段的寡脱氧核糖核苷酸(oligos)进行的竞争实验表明,对结构的要求比对序列的要求更严格。该元件可能是胰岛素诱导信号级联的末端之一。

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