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磷酸烯醇式丙酮酸羧激酶基因中两个相距甚远的糖皮质激素反应元件的定位与特征分析

Location and characterization of two widely separated glucocorticoid response elements in the phosphoenolpyruvate carboxykinase gene.

作者信息

Petersen D D, Magnuson M A, Granner D K

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University Medical School, Nashville, Tennessee 37232.

出版信息

Mol Cell Biol. 1988 Jan;8(1):96-104. doi: 10.1128/mcb.8.1.96-104.1988.

Abstract

Chimeric genes were constructed by fusion of various regions of the 5'-flanking sequence from the phosphoenolpyruvate carboxykinase (GTP) (PEPCK) gene to the chloramphenicol acetyltransferase-coding sequence and to simian virus 40 splice and polyadenylation sequences. These were used to demonstrate that two glucocorticoid regulatory elements (GREs) combine to confer glucocorticoid responsiveness upon the PEPCK gene in H4IIE hepatoma cells. Both elements, a distal one whose 5' boundary is located between -1264 and -1111 base pairs and a proximal one located between -468 and -420 base pairs relative to the transcription initiation site, act independently, in various positions and orientations, and upon the heterologous thymidine kinase promoter. Each element accounts for half of the maximal response of the chimeric genes. Therefore, two widely separated enhancerlike elements contribute equally to the response of the PEPCK gene to glucocorticoid hormones. Neither of the PEPCK GREs contains the TGTTCT consensus sequence associated with most other GREs.

摘要

通过将磷酸烯醇式丙酮酸羧激酶(GTP)(PEPCK)基因5'侧翼序列的不同区域与氯霉素乙酰转移酶编码序列以及猿猴病毒40剪接和聚腺苷酸化序列融合,构建了嵌合基因。这些用于证明两个糖皮质激素调节元件(GREs)结合起来赋予H4IIE肝癌细胞中的PEPCK基因糖皮质激素反应性。这两个元件,一个远端元件,其5'边界位于相对于转录起始位点的-1264至-1111碱基对之间,另一个近端元件位于-468至-420碱基对之间,它们在不同位置和方向上独立起作用,并作用于异源胸苷激酶启动子。每个元件占嵌合基因最大反应的一半。因此,两个广泛分离的类增强子元件对PEPCK基因对糖皮质激素的反应贡献相等。PEPCK的GREs均不包含与大多数其他GREs相关的TGTTCT共有序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a3d/363086/11b45154a1a3/molcellb00061-0121-a.jpg

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