Involvement of ITF2 in the transcriptional regulation of melanogenic genes

J Biol Chem. 2001 Jul 27;276(30):28147-54. doi: 10.1074/jbc.M101626200. Epub 2001 May 29.

Abstract

In response to agouti signal protein, melanocytes switch from producing eumelanin to pheomelanin concomitant with the down-regulation of melanogenic gene transcription. We previously reported that a ubiquitous basic helix-loop-helix transcription factor, known as ITF2, is up-regulated during this switch, and we now report that treatment of melanocytes with melanocyte-stimulating hormone down-regulates expression of ITF2. To more fully characterize the involvement of ITF2 in regulating melanogenic gene transcription, ITF2 sense or antisense constructs were introduced into melan-a melanocytes. Gene and protein expression analyses and luciferase reporter assays using promoters from melanogenic genes showed that up-regulation of ITF2 suppressed melanogenic gene expression as well as the expression of Mitf, a melanocyte-specific transcription factor. In addition, stable ITF2 sense transfectants had significant reductions in pigmentation and a less dendritic phenotype compared with mock transfectants. In contrast, ITF2 antisense-transfected melanocytes were more pigmented and more dendritic. These results demonstrate that up-regulation of ITF2 during the pheomelanin switch is functionally significant and reveal that differential expression of a ubiquitous basic helix-loop-helix transcription factor can modulate expression of melanogenic genes and the differentiation of melanocytes.

MeSH terms

  • Animals
  • Antigens, Neoplasm
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Blotting, Northern
  • Cell Differentiation
  • Cyclic AMP / metabolism
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / physiology*
  • Dendritic Cells / metabolism
  • Down-Regulation
  • Genes, Reporter
  • Helix-Loop-Helix Motifs
  • Luciferases / metabolism
  • MART-1 Antigen
  • Melanins / metabolism
  • Melanocytes / metabolism*
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Microscopy, Electron
  • Models, Biological
  • Neoplasm Proteins / metabolism
  • Nerve Tissue Proteins*
  • Oligonucleotides, Antisense / metabolism
  • Phenotype
  • Plasmids / metabolism
  • Precipitin Tests
  • Promoter Regions, Genetic
  • Protein Isoforms
  • RNA, Messenger / metabolism
  • Ribonucleases / metabolism
  • TCF Transcription Factors
  • Trans-Activators / chemistry
  • Trans-Activators / physiology*
  • Transcription Factor 4
  • Transcription Factors / metabolism
  • Transcription, Genetic*
  • Transfection
  • Up-Regulation

Substances

  • Antigens, Neoplasm
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • DNA-Binding Proteins
  • MART-1 Antigen
  • Melanins
  • Mlana protein, mouse
  • Neoplasm Proteins
  • Nerve Tissue Proteins
  • Oligonucleotides, Antisense
  • Protein Isoforms
  • RNA, Messenger
  • TCF Transcription Factors
  • Tcf4 protein, mouse
  • Trans-Activators
  • Transcription Factor 4
  • Transcription Factors
  • pheomelanin
  • Cyclic AMP
  • Luciferases
  • Ribonucleases