COUP-TF and transcriptional co-regulators in adrenal steroidogenesis

Endocr Res. 2004 Nov;30(4):795-801. doi: 10.1081/erc-200044042.

Abstract

Chicken ovalbumin upstream promoter-transcription factors (COUP-TFs) and steroidogenic factor-1 (SF-1) play key roles in the transcriptional regulation of steroidogenic P450 genes. Transfection studies showed that SF-1 activated bovine CYP17 promoter activity, whereas COUP-TFs repressed it from the CRS2 element in a mutually exclusive manner in mouse adrenocortical Y-1 cells. COUP-TFI and SF-1 competitively bind to the Ad5 element of the human CYP11B2 gene promoter. Unexpectedly, overexpression of COUP-TFI increased the CYP11B2 promoter activity, whereas overexpression of SF-1 repressed it in human adrenocortical H295R cells. In cortisol-producing adrenal cortical adenomas, down-regulation of nuclear receptors, including COUP-TFs was found. We therefore screened for COUP-TFI-interacting proteins using a yeast two-hybrid system and have identified Ubc9 and PIAS1, SUMO-1 conjugating enzyme and ligase, respectively. Coexpression of Ubc9 and PIAS1 synergistically enhanced COUP-TFI-mediated trans-repression of CYP17 gene as well as transactivation of CYP11B2 gene. The SUMOylation-defective mutants of these proteins continued to function as co-regulators of COUP-TFI. These findings indicate that Ubc9 and PIAS1 can function as transcriptional co-regulators of COUP-TFI to modulate adrenal cortical steroidogenesis in a SUMOylation-independent manner.

MeSH terms

  • Adrenal Cortex / metabolism*
  • Animals
  • COUP Transcription Factors
  • Cattle
  • Cell Line
  • Cytochrome P-450 CYP11B2 / genetics
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology
  • Homeodomain Proteins
  • Humans
  • Protein Inhibitors of Activated STAT
  • Proteins / physiology
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Steroid / metabolism*
  • Receptors, Steroid / physiology
  • Steroid 17-alpha-Hydroxylase / genetics
  • Steroidogenic Factor 1
  • Steroids / biosynthesis*
  • Transcription Factors / metabolism*
  • Transcription Factors / physiology
  • Transcription, Genetic / physiology*
  • Transfection
  • Ubiquitin-Conjugating Enzymes / physiology

Substances

  • COUP Transcription Factors
  • DNA-Binding Proteins
  • Homeodomain Proteins
  • NR5A1 protein, human
  • Protein Inhibitors of Activated STAT
  • Proteins
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Steroid
  • Steroidogenic Factor 1
  • Steroids
  • Transcription Factors
  • steroidogenic factor 1, mouse
  • Steroid 17-alpha-Hydroxylase
  • Cytochrome P-450 CYP11B2
  • Ubiquitin-Conjugating Enzymes
  • ubiquitin-conjugating enzyme UBC9