Intracellular mechanisms of gonadotropin-stimulated gene expression in granulosa cells

Steroids. 1991 May;56(5):232-6. doi: 10.1016/0039-128x(91)90039-x.

Abstract

Previous studies have shown that the gonadotropins follicle-stimulating hormone and luteinizing hormone stimulate proopiomelanocortin (POMC) promoter activity and mRNA levels in ovarian granulosa cells. The objective of these studies was to determine the role of cAMP-dependent protein kinases (pKA) in gonadotropin-stimulated gene expression. Primary cultures of rat granulosa cells were transfected with a gene construct consisting of the POMC promoter (-150 to +63; designated pOMC-CAT) fused to the chloramphenicol acetyltransferase (CAT) reporter gene either alone or cotransfected with an expression plasmid (designated mutant RI), which overexpresses a mutant form of the murine RI subunit incapable of binding cAMP and serving as an irreversible inhibitor of the catalytic subunit of pKA. Follicle-stimulating hormone or isoproterenol caused a significant stimulation of pOMC-CAT activity in transfected cells. Cotransfection of pOMC-CAT with mutant RI caused a significant inhibition of basal pOMC-CAT activity and abolished the gonadotropin stimulation. As a control, transfection of the SV-40 viral enhancer-promoter fused to CAT (pSV2-CAT) was unresponsive to follicle-stimulating hormone stimulation and cotransfection with mutant RI had no significant effect on pSV2-CAT activity. These studies suggest that gonadotropin regulation of the POMC promoter is mediated by pKA and that promoter activity is stringently controlled by pKA.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cells, Cultured
  • Chloramphenicol O-Acetyltransferase / metabolism
  • Cyclic AMP / physiology*
  • Female
  • Follicle Stimulating Hormone / pharmacology*
  • Gene Expression Regulation / drug effects*
  • Gonadotropins, Equine / pharmacology*
  • Granulosa Cells / drug effects*
  • Granulosa Cells / metabolism
  • Plasmids / genetics
  • Protein Kinase Inhibitors
  • Protein Kinases / physiology*
  • Rats
  • Transfection / genetics

Substances

  • Gonadotropins, Equine
  • Protein Kinase Inhibitors
  • Follicle Stimulating Hormone
  • Cyclic AMP
  • Chloramphenicol O-Acetyltransferase
  • Protein Kinases