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
论文数: 0引用数: 0
h-index: 0
机构:UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
Wierman, ME
Xiong, XY
论文数: 0引用数: 0
h-index: 0
机构:UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
Xiong, XY
Kepa, JK
论文数: 0引用数: 0
h-index: 0
机构:UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
Kepa, JK
Spaulding, AJ
论文数: 0引用数: 0
h-index: 0
机构:UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
Spaulding, AJ
Jacobsen, BM
论文数: 0引用数: 0
h-index: 0
机构:UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
Jacobsen, BM
Fang, ZQ
论文数: 0引用数: 0
h-index: 0
机构:UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
Fang, ZQ
Nilaver, G
论文数: 0引用数: 0
h-index: 0
机构:UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
Nilaver, G
Ojeda, SR
论文数: 0引用数: 0
h-index: 0
机构:UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
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
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.