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大鼠线粒体苯二氮䓬受体编码基因中三个转录调控元件的鉴定。

Identification of three transcriptional regulatory elements in the rat mitochondrial benzodiazepine receptor-encoding gene.

作者信息

Oberto A, Longone P, Krueger K E

机构信息

Fidia-Georgetown Institute for the Neurosciences, Georgetown University School of Medicine, Washington, DC 20007, USA.

出版信息

Gene. 1995 Dec 29;167(1-2):255-60. doi: 10.1016/0378-1119(95)00686-9.

Abstract

The sequence upstream from the first exon in the rat mitochondrial benzodiazepine receptor-encoding gene (MBR) was analyzed for transcriptional promoter activity by three techniques: promoter deletion analysis in vectors containing the gene cat encoding chloramphenicol acetyltransferase, electrophoretic mobility shift analysis (EMSA) and DNase I protection assay. All three methods are in uniformity with the identification of at least three regulatory elements corresponding to locations -51/-33, -267/-249 and -555/-526. The most distal and proximal domains are positive-acting, whereas the element at -267/-249 acts in a negative manner. The positive-acting -51/-33 element contains the middle of three consensus Sp1-recognition sequences found in this region of the gene. Binding of Y1 cell nuclear protein to a DNA fragment corresponding to this region of the gene is competed by a synthetic oligodeoxyribonucleotide bearing the consensus Sp1-binding site sequence. These studies provide the first reported functional evidence localizing transcriptional elements of MBR.

摘要

利用三种技术分析了大鼠线粒体苯二氮䓬受体编码基因(MBR)第一个外显子上游的序列的转录启动子活性:在含有编码氯霉素乙酰转移酶的基因cat的载体中进行启动子缺失分析、电泳迁移率变动分析(EMSA)和DNase I保护试验。所有这三种方法都一致鉴定出至少三个对应于-51 / -33、-267 / -249和-555 / -526位置的调控元件。最远端和最近端结构域具有正向作用,而位于-267 / -249的元件则起负向作用。正向作用的-51 / -33元件包含该基因此区域中发现的三个共有Sp1识别序列的中间序列。Y1细胞核蛋白与对应于该基因此区域的DNA片段的结合被带有共有Sp1结合位点序列的合成寡脱氧核糖核苷酸所竞争。这些研究提供了首次报道的定位MBR转录元件的功能证据。

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