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

被引:45
作者
Wierman, ME
Xiong, XY
Kepa, JK
Spaulding, AJ
Jacobsen, BM
Fang, ZQ
Nilaver, G
Ojeda, SR
机构
[1] UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
[2] OREGON HLTH SCI UNIV, DEPT NEUROL, PORTLAND, OR 97201 USA
[3] OREGON HLTH SCI UNIV, OREGON REG PRIMATE RES CTR, DIV NEUROSCI, BEAVERTON, OR USA
关键词
D O I
10.1128/MCB.17.3.1652
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页码:1652 / 1665
页数:14
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