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POU 同源结构域转录因子 SCIP/Oct-6/Tst-1 对促性腺激素释放激素启动子活性的抑制作用:一种表型表达的调控机制?

Repression of gonadotropin-releasing hormone promoter activity by the POU homeodomain transcription factor SCIP/Oct-6/Tst-1: a regulatory mechanism of phenotype expression?

作者信息

Wierman M E, Xiong X, Kepa J K, Spaulding A J, Jacobsen B M, Fang Z, Nilaver G, Ojeda S R

机构信息

Department of Medicine, University of Colorado Health Science Center, Denver 80220, USA.

出版信息

Mol Cell Biol. 1997 Mar;17(3):1652-65. doi: 10.1128/MCB.17.3.1652.

Abstract

POU domain transcription factors are required for neuropeptide expression in selected subsets of hypothalamic neuroendocrine neurons. We now report that expression of the gonadotropin-releasing hormone (GnRH) gene, which controls sexual development, is regulated by the POU protein SCIP/Oct-6/Tst-1. Reverse transcriptase PCR cloning and RNase protection assays demonstrated the presence of SCIP/Oct-6/Tst-1 mRNA in the GnRH-producing neuronal cell line GT1-7. The physiological relevance of this regulatory activity was suggested by the detection of SCIP/Oct-6/Tst-1 mRNA in a subset of GnRH neurons in the hypothalamus of prepubertal female rats. Coexpression of SCIP/Oct-6/Tst-1 in neuronal cells inhibited rat GnRH (rGnRH) promoter activity via three regions of the proximal rGnRH promoter containing SCIP/Oct-6/Tst-1 binding sites. DNase I footprinting, gel shift assays, and DNA and protein mutagenesis studies indicated that both direct DNA binding and protein-protein interactions are required for SCIP/Oct-6/Tst-1 modulation of GnRH gene expression. Activation of SCIP/Oct-6/Tst-1 expression in terminally differentiated GnRH neurons may be a factor determining the ratio of phenotypically "inactive" versus "active" GnRH neurons during postnatal life.

摘要

POU结构域转录因子是下丘脑神经内分泌神经元特定亚群中神经肽表达所必需的。我们现在报告,控制性发育的促性腺激素释放激素(GnRH)基因的表达受POU蛋白SCIP/Oct-6/Tst-1调控。逆转录酶PCR克隆和核糖核酸酶保护分析证明,在产生GnRH的神经元细胞系GT1-7中存在SCIP/Oct-6/Tst-1 mRNA。在青春期前雌性大鼠下丘脑的一部分GnRH神经元中检测到SCIP/Oct-6/Tst-1 mRNA,提示了这种调节活性的生理相关性。SCIP/Oct-6/Tst-1在神经元细胞中的共表达通过近端rGnRH启动子的三个含有SCIP/Oct-6/Tst-1结合位点的区域抑制大鼠GnRH(rGnRH)启动子活性。DNA酶I足迹法、凝胶迁移分析以及DNA和蛋白质诱变研究表明,SCIP/Oct-6/Tst-1对GnRH基因表达的调节既需要直接的DNA结合,也需要蛋白质-蛋白质相互作用。在终末分化的GnRH神经元中激活SCIP/Oct-6/Tst-1的表达可能是决定出生后生活中表型“无活性”与“有活性”的GnRH神经元比例的一个因素。

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