Gonadotropin regulation of the rat proopiomelanocortin promoter: Characterization by transfection of primary ovarian granulosa cells

S. L. Young, C. P. Nielsen, James Lundblad, J. L. Roberts, M. H. Melner

Research output: Contribution to journalArticle

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Abstract

To characterize the transcriptional effects of human (h)FSH and hCG on the POMC gene, primary rat granulosa cells were transiently transfected with a chloramphenicol acetyltransferase (CAT) reporter plasmid under the control of the POMC promoter and 5' region. POMC-CAT contains a fragment of the rat POMC gene, extending from nucleotide -704 to nucleotide +63, fused to the CAT gene. Treatment of POMC-CAT-transfected cells with either hFSH (20 ng/ml) or hCG (10 ng/ml) significantly increased CAT enzyme activity; however, neither hCG nor hFSH increased CAT enzyme activity in cells tranfected with pSV2-CAT, a reported plasmid under the control of the SV40 virus promoter and 5' region. The phosphodiesterase inhibitor isobutylmethylxanthine or the nonhydrolyzable cAMP analog cAMP-chlorothiophenyl significantly increased CAT activity in POMC-CAT-transfected granulosa cells. Human FSH stimulated transcription 10, 20, and 40 h after treatment, but FSH stimulation at the two earlier time points was 2.5- to 5.5-fold greater than that at 40 h. Gonadotropin-stimulated steroidogenesis was equivalent in POMC-CAT-transfected granulosa cells, untransfected, and mock-transfected cells. This indicates that transfection left the physiological hormone response intact. These data demonstrate the following. 1) 767 basepairs of the rat POMC gene are enough to confer gonadotropin stimulation on the CAT marker gene in granulosa cells. 2) Although the POMC promoter lacks a well conserved cAMP response element, either of two different pharmacological manipulations of granulosa cells that raise intracellular cAMP can also stimulate POMC-driven CAT expression. 3) Transfected primary cultures of granulosa cells provide a nontransformed, physiologically relevant model with which to study hormone-regulated gene expression.

Original languageEnglish (US)
Pages (from-to)15-21
Number of pages7
JournalMolecular Endocrinology
Volume3
Issue number1
StatePublished - 1989

Fingerprint

Pro-Opiomelanocortin
Chloramphenicol O-Acetyltransferase
Granulosa Cells
Gonadotropins
Transfection
Human Follicle Stimulating Hormone
Genes
Genetic Promoter Regions
Plasmids
Nucleotides
Hormones
Phosphodiesterase Inhibitors
Simian virus 40
Response Elements
Enzymes

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology, Diabetes and Metabolism

Cite this

Gonadotropin regulation of the rat proopiomelanocortin promoter : Characterization by transfection of primary ovarian granulosa cells. / Young, S. L.; Nielsen, C. P.; Lundblad, James; Roberts, J. L.; Melner, M. H.

In: Molecular Endocrinology, Vol. 3, No. 1, 1989, p. 15-21.

Research output: Contribution to journalArticle

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