Peroxisome proliferator-activated receptor α induces rat sterol carrier protein x promoter activity through two peroxisome proliferator- response elements

Dayami Lopez, Rosalyn B. Irby, Mark P. McLean

Research output: Contribution to journalArticle

15 Scopus citations


Sterol carrier protein x (SCPx) plays a critical role in the peroxisomal oxidation of fatty acids. It has been previously demonstrated in streptozotocin-induced diabetic rats that SCPx expression is induced in association with an elevation in serum fatty acid and triglyceride levels. To elucidate the mechanisms underlying the expression of this gene during diabetes, the rat SCPx promoter was cloned and analyzed for regulatory motifs. Sequence analysis of this TATA-less promoter revealed two putative peroxisomal- proliferator-response element (PPRE) binding motifs at positions -134 and -869 relative to the translation start site. To examine peroxisomal-proliferator- activated receptor α (PPARα) effects on this gene, 935 bp of the SCPx promoter containing both PPRE motifs was cloned in front of the chloramphenicol acetyl-transferase gene or the luciferase gene and co-transfected into HTB-9 cells with vectors that encoded for PPARα and retinoid X receptor (RXR). The results indicate that PPARα was able to induce SCPx promoter activity in both cases, an effect that was enhanced by RXR and clofibrate. In addition, mutational analysis studies demonstrated that both PPREs contributed to the PPARα/RXRα-dependent activation of the SCPx promoter. Mobility shift assays and supershift analysis showed that nuclear extracts containing PPARα bound to the two PPRE motifs. This investigation indicates that similar to other genes involved in β-oxidation, SCPx transcription may be controlled by fatty acid levels via PPARα.

Original languageEnglish (US)
Pages (from-to)169-184
Number of pages16
JournalMolecular and Cellular Endocrinology
Issue number1-2
Publication statusPublished - Jul 31 2003


All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology
  • Endocrinology

Cite this