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VI类POU蛋白mPOU(Brn-5)参与Pit-1以及催乳素的基因表达。

Involvement of mPOU (Brn-5), a class VI POU protein, in the gene expression of Pit-1 as well as PRL.

作者信息

Toda Keizo, Yamamoto Daisuke, Fumoto Mariko, Ikeshita Nobuko, Herningtyas Elizabeth Henny, Iida Keiji, Takahashi Yutaka, Kaji Hidesuke, Chihara Kazuo, Okimura Yasuhiko

机构信息

Department of Basic Allied Medicine, Kobe University School of Medicine, 7-10-2, Tomogaoka, Suma-ku, Kobe 654-0142, Japan.

出版信息

Mol Cell Endocrinol. 2008 Jan 2;280(1-2):20-9. doi: 10.1016/j.mce.2007.09.002. Epub 2007 Sep 8.

Abstract

PRL is mainly expressed in the pituitary and its gene expression is regulated by a variety of transcription factors including Pit-1. Brn-5 is a transcription factor that binds to Pit-1 binding elements and stimulates PRL reporter gene expression. In this study, the role of Brn-5 was examined. RNA interference (RNAi) against Brn-5 leaded to reduction in PRL content of GH3 cells, indicating endogenous Brn-5 may play a role in PRL gene expression. Furthermore Brn-5 RNAi decreased Pit-1 mRNA. Transfection of expression vectors for mPOU (human ortholog of Brn-5) modestly but significantly stimulated activities of PRL-Luc and Pit-1-Luc reporter genes in GH3 and HEK 293 cells. In addition, mPOU showed synergistic action with Pit-1 and CBP on PRL-Luc expression. mPOU-FL, a splicing variant of mPOU, showed weaker activity than mPOU. Chip assay suggested binding of mPOU to PRL and Pit-1 promoters of genomic DNA. Taken together, these results suggest that mPOU (Brn-5) enhances PRL gene expression directly in association with Pit-1 and CBP, and indirectly via the activation of Pit-1 gene expression.

摘要

催乳素(PRL)主要在垂体中表达,其基因表达受包括Pit-1在内的多种转录因子调控。Brn-5是一种转录因子,它与Pit-1结合元件结合并刺激PRL报告基因表达。在本研究中,对Brn-5的作用进行了检测。针对Brn-5的RNA干扰(RNAi)导致GH3细胞中PRL含量降低,表明内源性Brn-5可能在PRL基因表达中发挥作用。此外,Brn-5 RNAi降低了Pit-1 mRNA水平。转染mPOU(Brn-5的人类直系同源物)表达载体适度但显著地刺激了GH3和HEK 293细胞中PRL-Luc和Pit-1-Luc报告基因的活性。此外,mPOU在PRL-Luc表达上与Pit-1和CBP表现出协同作用。mPOU-FL是mPOU的一种剪接变体,其活性比mPOU弱。染色质免疫沉淀分析表明mPOU与基因组DNA的PRL和Pit-1启动子结合。综上所述,这些结果表明mPOU(Brn-5)直接与Pit-1和CBP相关联增强PRL基因表达,并通过激活Pit-1基因表达间接增强PRL基因表达。

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