Melanocytes and the microphthalmia transcription factor network

• Published in: Annual review of genetics Vol. 38; no. 1; pp. 365 - 411
• Main Authors: Steingrímsson, Eiríkur, Copeland, Neal G, Jenkins, Nancy A
• Format: Journal Article
• Language: English
• Published: United States Annual Reviews, Inc 01-01-2004
• Subjects: Alleles; Animals; Cell Line, Tumor; Chromosome Mapping; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Gene Expression Regulation, Developmental; Gene Expression Regulation, Neoplastic; Genetics; Humans; Melanocytes - metabolism; Melanoma; Melanoma - genetics; Mice; Microphthalmia-Associated Transcription Factor; Models, Genetic; Multigene Family; Mutation; Nuclear Proteins - metabolism; Phenotype; Sarcoma; Signal Transduction; Trans-Activators - metabolism; Transcription Factors - genetics; Transcription Factors - metabolism; Waardenburg Syndrome - genetics
• ISSN: 0066-4197; 1545-2948
• DOI: 10.1146/annurev.genet.38.072902.092717

The first mouse microphthalmia transcription factor (Mitf ) mutation was discovered over 60 years ago, and since then over 24 spontaneous and induced mutations have been identified at the locus. Mitf encodes a member of the Myc supergene family of basic helix-loop-helix zipper (bHLH-Zip) transcription factors. Like Myc, Mitf regulates gene expression by binding to DNA as a homodimer or as a heterodimer with another related family member, in the case of Mitf the Tfe3, Tfeb, and Tfec proteins. The study of Mitf has provided many insights into the biology of melanocytes and helped to explain how melanocyte-specific gene expression and signaling is regulated. The human homologue of MITF is mutated in patients with the pigmentary and deafness disorder Waardenburg Syndrome Type 2A (WS2A). The mouse Mitf mutations therefore serve as a model for the study of this human disease. Mutations and/or aberrant expression of several MITF family member genes have also been reported in human cancer, including melanoma (MITF), papillary renal cell carcinoma (TFE3, TFEB), and alveolar soft part sarcoma (TFE3). Genes in the MITF/TFE pathway may therefore also represent valuable therapeutic targets for the treatment of human cancer. Here we review recent developments in the analysis of Mitf function in vivo and in vitro and show how traditional genetics, modern forward genetics and in vitro biochemical analyses have combined to produce an intriguing story on the role and actions of a gene family in a living organism.