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编码人2-酮戊二酸脱氢酶基因5'-侧翼区的功能特性分析

Functional characterization of the 5'-flanking region of the gene encoding human 2-oxoglutarate dehydrogenase.

作者信息

Koike K, Matsuo S

机构信息

Department of Pathological Biochemistry, Atomic Disease Institute, Nagasaki University School of Medicine, Sakamoto, Japan.

出版信息

Gene. 1997 Feb 20;186(1):45-53. doi: 10.1016/s0378-1119(96)00677-4.

Abstract

The 5'-flanking region of the gene (OGDH) encoding human 2-oxoglutarate dehydrogenase (OGDH) does not contain TATA or CAAT boxes, but contains an inverted GC box. To identify a functional OGDH promoter, systematic transient expression analysis of the 5'-flanking region (wild type, -3276/+212) of the OGDH was performed using serially nested deletions and linker-scanning mutations. The OGDH (wild type)-luciferase (LUC) reporter vector (pGV-E) construct and its deletion or linker-mutant constructs were transfected into BHK-21 cells and LUC activity was assessed. The OGDH-LUC construct expressed reproducibly >12-fold more LUC activity than did a control pGV-E vector. The promoter activity was up-regulated by treatment with 2-oxoglutarate and 2-oxoglutarate/glutamate. Deletions of sequences between nt -563 and -62 (M6 and M7) resulted in a 2-fold increase in LUC activity. Further deletion of the sequence between nt -61 and +212 (M8-M10) abolished LUC activity. High resolution mutagenesis within the -113 to -14 region indicated that the -53 to -44 and -33 to -24 sequences were required for positive regulation and the -93 to -84 sequence for negative regulation. We have identified a nuclear factor that binds to nt -63 to -24 including two cis-acting sites.

摘要

编码人2-氧代戊二酸脱氢酶(OGDH)的基因(OGDH)的5'侧翼区域不含TATA或CAAT框,但含有一个反向GC框。为了鉴定功能性OGDH启动子,使用连续嵌套缺失和接头扫描突变对OGDH的5'侧翼区域(野生型,-3276 / + 212)进行了系统的瞬时表达分析。将OGDH(野生型)-荧光素酶(LUC)报告载体(pGV-E)构建体及其缺失或接头突变体构建体转染到BHK-21细胞中,并评估LUC活性。与对照pGV-E载体相比,OGDH-LUC构建体可重复表达的LUC活性高12倍以上。用2-氧代戊二酸和2-氧代戊二酸/谷氨酸处理可上调启动子活性。缺失nt -563和-62之间的序列(M6和M7)导致LUC活性增加2倍。进一步缺失nt -61和+212之间的序列(M8-M10)消除了LUC活性。在-113至-14区域内的高分辨率诱变表明,-53至-44和-33至-24序列是正调控所必需的,而-93至-84序列是负调控所必需的。我们已经鉴定出一种与nt -63至-24结合的核因子,其中包括两个顺式作用位点。

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