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一种垂体特异性因子与大鼠生长激素基因中的上游启动子元件相互作用。

A pituitary-specific factor interacts with an upstream promotor element in the rat growth hormone gene.

作者信息

Catanzaro D F, West B L, Baxter J D, Reudelhuber T L

机构信息

Department of Biological Sciences, University of Sydney, New South Wales, Australia.

出版信息

Mol Endocrinol. 1987 Jan;1(1):90-6. doi: 10.1210/mend-1-1-90.

Abstract

The expression of the rat GH (rGH) gene is limited to the anterior pituitary. Using a DNase I footprinting assay, we have sought to identify specific protein-DNA interactions in the rGH 5'-flanking DNA that may be important in conferring tissue-specific use of the rGH promoter. We have identified a nuclear factor from rGH-secreting GC (rat pituitary) cells which interacts in the rGH 5'-flanking DNA between positions -94 to -62 relative to the start site of rGH gene transcription. This factor, which we have named GC1, is undetectable in nuclear extracts of non-rGH-producing rat fibroblast (Rat-2), or HeLa cells. Mutation of the GC1 binding region in the rGH 5'-flanking DNA results in only a small (30%) decrease in the ability of the rGH promoter to drive the expression of a linked marker gene when transfected into GC cells. GC1 represents, therefore, a novel type of promoter binding factor which is gene-specific and whose distribution is tissue-specific, but which is nonessential for the basal expression of its linked gene. Such a factor may, however, play a role in the modulation of rGH gene expression either through its interaction with other regulatory proteins or ligands or after enzyme modification.

摘要

大鼠生长激素(rGH)基因的表达仅限于垂体前叶。我们利用DNA酶I足迹分析,试图确定rGH 5'侧翼DNA中特定的蛋白质-DNA相互作用,这些相互作用可能对赋予rGH启动子组织特异性使用至关重要。我们从分泌rGH的GC(大鼠垂体)细胞中鉴定出一种核因子,它在相对于rGH基因转录起始位点-94至-62位的rGH 5'侧翼DNA中相互作用。我们将这种因子命名为GC1,在不产生rGH的大鼠成纤维细胞(Rat-2)或HeLa细胞的核提取物中无法检测到。rGH 5'侧翼DNA中GC1结合区域的突变,在转染到GC细胞时,仅导致rGH启动子驱动连接的标记基因表达的能力小幅(30%)下降。因此,GC1代表了一种新型的启动子结合因子,它具有基因特异性且分布具有组织特异性,但对其连接基因的基础表达并非必需。然而,这种因子可能通过与其他调节蛋白或配体相互作用,或在酶修饰后,在rGH基因表达的调节中发挥作用。

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