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TEAD1抑制培养的人子宫蜕膜细胞中催乳素基因的表达。

TEAD1 inhibits prolactin gene expression in cultured human uterine decidual cells.

作者信息

Kessler Cherie A, Bachurski Cindy J, Schroeder Jennifer, Stanek Jerzy, Handwerger Stuart

机构信息

Divisions of Endocrinology, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, United States.

出版信息

Mol Cell Endocrinol. 2008 Nov 25;295(1-2):32-8. doi: 10.1016/j.mce.2008.08.007. Epub 2008 Aug 19.

Abstract

Forced overexpression of TEAD1 in human uterine fibroblast (HUF) and human endometrial stromal cells markedly inhibited prolactin promoter activity in both cell types in a dose-dependent manner, with maximal inhibition of greater than 90%. Conversely, the knockdown of TEAD1 expression in HUF cells with a TEAD1 siRNA resulted in a 75-80% increase in prolactin mRNA levels (p<0.01) compared to control cells exposed to a scrambled nonsense RNA. Mutagenesis of the putative TEAD site inhibited basal promoter activity by about 80%. However, mutagenesis of the TEAD site did not prevent TEAD1-induced inhibition of promoter activity; and the transcription activity of a minimal promoter fragment lacking a putative TEAD binding site was repressed by overexpression of TEAD1. Taken together, these findings suggest that the TEAD binding site on the prolactin promoter is important for the maintenance of basal prolactin promoter activity and that overexpression of TEAD1 has a dominant-negative effect on prolactin promoter activity, probably by interacting directly with other transcription factors.

摘要

在人子宫成纤维细胞(HUF)和人子宫内膜基质细胞中强制过表达TEAD1,可在两种细胞类型中以剂量依赖性方式显著抑制催乳素启动子活性,最大抑制率超过90%。相反,与暴露于乱序无义RNA的对照细胞相比,用TEAD1 siRNA敲低HUF细胞中TEAD1的表达导致催乳素mRNA水平增加75 - 80%(p<0.01)。假定的TEAD位点诱变使基础启动子活性降低约80%。然而,TEAD位点诱变并未阻止TEAD1诱导的启动子活性抑制;并且缺乏假定TEAD结合位点的最小启动子片段的转录活性被TEAD1过表达所抑制。综上所述,这些发现表明催乳素启动子上的TEAD结合位点对于维持基础催乳素启动子活性很重要,并且TEAD1的过表达对催乳素启动子活性具有显性负性作用,可能是通过直接与其他转录因子相互作用实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bfb/2615051/4fa9200ac0c9/nihms79428f1.jpg

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