Negative regulation of c-Myc transcription by pancreas duodenum homeobox-1

Endocrinology. 2007 May;148(5):2168-80. doi: 10.1210/en.2006-1221. Epub 2007 Feb 22.

Abstract

The pancreatic and duodenal homeobox factor-1 (Pdx1) is essential for pancreatic development and insulin gene transcription, whereas c-Myc has a deleterious effect on islet function. However, the relationship between c-Myc and Pdx1 is poorly concerned. Here we demonstrated that Pdx1 could suppress c-Myc promoter activity, which relied on T cell factor (Tcf) binding elements harbored in c-Myc promoter. Furthermore, the transcription activity of beta-catenin/Tcf was markedly decreased on Pdx1 expression, but cotransfection of Pdx1 short hairpin RNA abrogated this effect. Pdx1 expression did not induce beta-catenin degradation nor did it alter their subcellular distribution. The mutation analysis showed that the amino acids (1-209) of Pdx1 harboring an inhibitory domain, which might lead to the reduction of beta-catenin/Tcf/p300 complex levels and attenuate their binding activity with c-Myc promoter sequences. Moreover, adenovirus-mediated Pdx1 interference caused cell proliferation and cytokine-induced apoptosis via the dysregulation of c-Myc transcription. These results indicated that the Pdx1 functioned as a key regulator for maintenance of beta-cell function, at least in part, through controlling c-Myc expression and the loss of its regulatory function may be an alternative mechanism for beta-cell neogenesis and apoptosis found in diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Carcinoma, Hepatocellular
  • Cell Division / physiology
  • Cell Line, Tumor
  • Down-Regulation / physiology
  • Genes, Reporter
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / metabolism*
  • Humans
  • Insulin-Secreting Cells / cytology*
  • Insulin-Secreting Cells / physiology*
  • Liver Neoplasms
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Promoter Regions, Genetic / physiology
  • Proto-Oncogene Proteins c-myc / genetics*
  • Proto-Oncogene Proteins c-myc / metabolism
  • Signal Transduction / physiology
  • TCF Transcription Factors / genetics
  • Trans-Activators / genetics*
  • Trans-Activators / metabolism*
  • Transcription Factor 7-Like 2 Protein
  • Transcriptional Activation / physiology
  • Transfection
  • beta Catenin / genetics
  • beta Catenin / metabolism

Substances

  • Homeodomain Proteins
  • Proto-Oncogene Proteins c-myc
  • TCF Transcription Factors
  • TCF7L2 protein, human
  • Tcf7l2 protein, mouse
  • Trans-Activators
  • Transcription Factor 7-Like 2 Protein
  • beta Catenin
  • pancreatic and duodenal homeobox 1 protein