Evidence that functional interactions of CREB and SF-1 mediate hormone regulated expression of the aromatase gene in granulosa cells and constitutive expression in R2C cells

J Steroid Biochem Mol Biol. 1997 Apr;61(3-6):223-31.

Abstract

The proximal promoter of the rat aromatase CYP19 gene contains two functional domains that can confer hormone/cAMP inducibility in primary cultures of rat granulosa cells and constitutive expression in R2C Leydig cells. Region A contains a hexameric sequence that binds steroidogenic factor-1 (SF-1). Region B contains a CRE-like sequence that binds CREB and two other factors, X and Y. To determine if CRE binding factors X and Y had overlapping functions with CREB, and to determine if the CREB and SF-1 binding sites exhibited functional interactions in the context of the intact promoter, mutations within the CRE and hexameric SF-1 binding site were generated. Mutations within the CRE showed that CREB but not factors X and Y mediated cAMP-dependent activity of chimeric transgenes in primary granulosa cell cultures. Granulosa cells transfected with constructs that bound CREB but not SF-1 (or the converse) resulted in a loss of approximately 50% cAMP-dependent CAT activity. Transgenes that did not bind CREB or SF-1 exhibited no cAMP-dependent CAT activity. When these same constructs where transfected into R2C Leydig cells, mutation of either the CREB or SF-1 binding sites resulted in a greater than 90% loss of CAT activity. Western blot and immunocytochemistry analyses revealed that the amount of phosphorylated CREB increased in response to hormone/cAMP in granulosa cells and was high in R2C Leydig cells, coinciding with expression of the transgenes and endogenous aromatase mRNA in each cell type. Therefore, in both cell types the aromatase promoter is dependent upon a functional CRE and the presence of phosphoCREB. The CREB and SF-1 binding sites interact in an additive manner to mediate cAMP transactivation in granulosa cells, whereas they interact synergistically to confer high basal transactivation in R2C Leydig cells. Taken together, the results indicated that the molecular mechanisms or pathways that activate CREB, SF-1 or their interaction are different in granulosa cells and R2C cells.

MeSH terms

  • Animals
  • Aromatase / genetics*
  • Aromatase / metabolism
  • CREB-Binding Protein
  • Cells, Cultured
  • Cyclic AMP / pharmacology
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Female
  • Fushi Tarazu Transcription Factors
  • Gene Expression Regulation, Enzymologic* / drug effects
  • Gene Transfer Techniques
  • Granulosa Cells / enzymology*
  • Homeodomain Proteins
  • Hormones / pharmacology
  • Leydig Cells / enzymology*
  • Male
  • Mutation
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Promoter Regions, Genetic / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Cytoplasmic and Nuclear
  • Steroidogenic Factor 1
  • Trans-Activators*
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • DNA-Binding Proteins
  • Fushi Tarazu Transcription Factors
  • Homeodomain Proteins
  • Hormones
  • Nuclear Proteins
  • Receptors, Cytoplasmic and Nuclear
  • Steroidogenic Factor 1
  • Trans-Activators
  • Transcription Factors
  • steroidogenic factor 1, rat
  • Cyclic AMP
  • Aromatase
  • CREB-Binding Protein
  • Crebbp protein, rat