1. Academic Validation
  2. Identification of a novel isoform of microphthalmia-associated transcription factor that is enriched in retinal pigment epithelium

Identification of a novel isoform of microphthalmia-associated transcription factor that is enriched in retinal pigment epithelium

  • Biochem Biophys Res Commun. 1998 Jun 29;247(3):710-5. doi: 10.1006/bbrc.1998.8838.
S Amae 1 N Fuse K Yasumoto S Sato I Yajima H Yamamoto T Udono Y K Durlu M Tamai K Takahashi S Shibahara
Affiliations

Affiliation

  • 1 Department of Molecular Biology and Applied Physiology, Tohoku University School of Medicine, Miyagi, Japan.
Abstract

Mutations at the mouse locus encoding microphthalmia-associated transcription factor (Mitf) affect the development of many cell types, including retinal pigment epithelium (RPE), melanocytes, mast cells, and osteoclasts. Here we have identified a novel Mitf isoform, Mitf-a, and its human homologue MITF-A by cDNA cloning. MITF-A consists of 520 amino acid residues and differs in the amino-terminus from authentic melanocyte-type MITF (MITF-M). MITF-A mRNA is widely expressed and represents a predominant MITF isoform in cultured RPE cells, whereas MITF-M mRNA is exclusively expressed in melanocytes and melanoma cells. In situ hybridization analysis suggested that Mitf-a mRNA is enriched in the prospective RPE of mouse embryo. Moreover, transient cotransfection assays suggested that MITF-A activated transcription of the Tyrosinase and tyrosinase-related protein 1 genes. MITF-A/Mitf-a therefore may play an important role in melanogenesis in RPE.

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