Regulation of pigment cell-specific gene expression by MITF

Shigeki Shibahara, Ken Ichi Yasumoto, Shintaro Amae, Tetsuo Udono, Ken Ichi Watanabe, Hideo Saito, Kazuhisa Takeda

Research output: Contribution to journalArticlepeer-review

77 Citations (Scopus)

Abstract

Melanocyte and retinal pigment epithelium (RPE) specifically express tyrosinase and other melanin-producing enzymes. Microphthalmia-associated transcription factor (Mitf), encoded at the mouse microphthalmia locus, regulates the development and survival of many cell types, including melanocyte and RPE. MITF, the human homolog of Mitf, consists of at least four isoforms with distinct amino-termini, referred to as A, MITF-C, MITF-H, and MITF-M. MITF-M is exclusively expressed in melanocytes and melanoma cells, and thus represents the melanocyte lineage-specific isoform. In contrast, other isoforms are expressed in many cell types so far examined. These isoforms appear to function as transcriptional activators of the melanogenesis genes, as assessed by transient transfection assays in cultured cells. Functional significance of Mitf-M in melanocyte differentiation was verified by the molecular lesion of black-eyed white Mitfmi-bw mice, which lack melanocytes but have normal RPE. The Mitf gene of this mutant has the insertion of an L1 retrotransposable element in the intron between exon 3 and exon 4, leading to complete repression of Mitf-M mRNA expression. Taken together, these results suggest that melanogenesis in melanocyte and RPE is regulated by separate Mitf/MITF isoforms. Recent findings on the multiplicity of MITF isoforms are summarized.

Original languageEnglish
Pages (from-to)98-102
Number of pages5
JournalPigment Cell Research
Volume13
Issue numberSUPPL. 8
DOIs
Publication statusPublished - 2000

Keywords

  • Differentiation
  • Melanin
  • Melanocyte
  • Retinal pigment epithelium
  • Transcription

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