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[XBP-1增强雌激素受体α的转录活性]

[XBP-1 enhances the transcriptional activity of estrogen receptor alpha].

作者信息

Ding Li-Hua, Ye Qi-Nong, Zhu Jian-Hua, Yan Jing-Hua, Zhong Hong-Jun, Wang Zong-Hua, Huang Cui-Fen

机构信息

Beijing Institute of Biotechnology, Beijing 100850, China.

出版信息

Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003 Sep;35(9):829-33.

Abstract

The estrogen receptor (ERalpha) is a member of a large superfamily of nuclear receptors that regulates the transcription of estrogen-responsive genes. Several recent studies have demonstrated that human X-box binding protein 1 (XBP-1) mRNA expression is associated with ERalpha status in breast tumors. More recently, two forms of XBP-1 were identified due to their unique splicing. The two splicing variants of XBP-1 were designated XBP-1S and XBP-1U, respectively. In this study, the coding sequences of XBP-1S and XBP-1U were cloned respectively into the expression vector pcDNA3 harboring FLAG epitope, generating the recombinant plasmids pcDNA3-FLAG-XBP-1S and pcDNA3-FLAG-XBP-1U. Western blot analysis showed that both XBP-1S and XBP-1U were expressed in mammalian cells. To determine the effects of XBP-1S and XBP-1U on the transcriptional activity of ERalpha, MDA-MB-231 breast cancer cells were cotransfected with the expression vectors for ERalpha and either pcDNA3-FLAG-XBP-1S or pcDNA3-FLAG-XBP-1U. The results indicated that XBP-1S and XBP-1U enhanced ERalpha-mediated transcriptional activities in a hormone-independent manner. GST pull-down assay showed that both XBP-1S and XBP-1U interacted with ERalpha. These data suggest that XBP-1S and XBP-1U may play an important role in breast cancer growth and progression through ERalpha signaling.

摘要

雌激素受体(ERα)是核受体大家族的成员之一,可调节雌激素反应性基因的转录。最近的几项研究表明,人类X盒结合蛋白1(XBP-1)mRNA表达与乳腺肿瘤中的ERα状态相关。最近,由于其独特的剪接方式,鉴定出了两种形式的XBP-1。XBP-1的两种剪接变体分别命名为XBP-1S和XBP-1U。在本研究中,分别将XBP-1S和XBP-1U的编码序列克隆到带有FLAG表位的表达载体pcDNA3中,构建了重组质粒pcDNA3-FLAG-XBP-1S和pcDNA3-FLAG-XBP-1U。蛋白质免疫印迹分析表明,XBP-1S和XBP-1U均在哺乳动物细胞中表达。为了确定XBP-1S和XBP-1U对ERα转录活性的影响,将ERα表达载体与pcDNA3-FLAG-XBP-1S或pcDNA3-FLAG-XBP-1U共转染MDA-MB-231乳腺癌细胞。结果表明,XBP-1S和XBP-1U以激素非依赖性方式增强了ERα介导的转录活性。谷胱甘肽-S-转移酶下拉实验表明,XBP-1S和XBP-1U均与ERα相互作用。这些数据表明,XBP-1S和XBP-1U可能通过ERα信号通路在乳腺癌的生长和进展中发挥重要作用。

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