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结缔组织生长因子抑制雌激素受体转录活性。

Suppression of estrogen receptor transcriptional activity by connective tissue growth factor.

机构信息

Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.

出版信息

PLoS One. 2011;6(5):e20028. doi: 10.1371/journal.pone.0020028. Epub 2011 May 24.

Abstract

Secreted growth factors have been shown to stimulate the transcriptional activity of estrogen receptors (ER) that are responsible for many biological processes. However, whether these growth factors physically interact with ER remains unclear. Here, we show for the first time that connective tissue growth factor (CTGF) physically and functionally associates with ER. CTGF interacted with ER both in vitro and in vivo. CTGF interacted with ER DNA-binding domain. ER interaction region in CTGF was mapped to the thrombospondin type I repeat, a cell attachment motif. Overexpression of CTGF inhibited ER transcriptional activity as well as the expression of estrogen-responsive genes, including pS2 and cathepsin D. Reduction of endogenous CTGF with CTGF small interfering RNA enhanced ER transcriptional activity. The interaction between CTGF and ER is required for the repression of estrogen-responsive transcription by CTGF. Moreover, CTGF reduced ER protein expression, whereas the CTGF mutant that did not repress ER transcriptional activity also did not alter ER protein levels. The results suggested the transcriptional regulation of estrogen signaling through interaction between CTGF and ER, and thus may provide a novel mechanism by which cross-talk between secreted growth factor and ER signaling pathways occurs.

摘要

已发现分泌型生长因子可刺激雌激素受体(ER)的转录活性,而后者负责许多生物过程。然而,这些生长因子是否与 ER 发生物理相互作用尚不清楚。在这里,我们首次表明结缔组织生长因子(CTGF)与 ER 发生物理和功能相互作用。CTGF 在体外和体内均与 ER 相互作用。CTGF 与 ER 的 DNA 结合域相互作用。CTGF 中与 ER 相互作用的区域被映射到血栓反应蛋白 I 型重复序列,这是一个细胞附着基序。CTGF 的过表达抑制 ER 的转录活性以及雌激素反应基因的表达,包括 pS2 和组织蛋白酶 D。用 CTGF 小干扰 RNA 降低内源性 CTGF 增强了 ER 的转录活性。CTGF 与 ER 之间的相互作用是 CTGF 抑制雌激素反应转录所必需的。此外,CTGF 降低 ER 蛋白表达,而不抑制 ER 转录活性的 CTGF 突变体也不改变 ER 蛋白水平。这些结果表明通过 CTGF 与 ER 之间的相互作用对雌激素信号转导进行转录调控,从而为分泌型生长因子与 ER 信号通路之间的串扰提供了一种新的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9927/3101213/ae9b317a10fb/pone.0020028.g001.jpg

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