INSERM U895, Equipe 1, Biologie et Pathologies des cellules mélanocytaires, NICE Cedex 2, France.
Pigment Cell Melanoma Res. 2010 Feb;23(1):27-40. doi: 10.1111/j.1755-148X.2009.00653.x. Epub 2009 Nov 25.
Microphthalmia-associated transcription factor (MITF) was initially shown to play a key role in melanocyte differentiation through the direct transcriptional control of TYROSINASE, TYRP1 and DCT genes, encoding the three enzymes involved in melanin synthesis or melanogenesis. Sixteen years after the first description of MITF, more than 40 direct MITF target genes have been described. They play a key role in melanocyte, osteoclast and mast cell specific functions. Furthermore, several MITF target genes, e.g. BCL2, CDK2, CDKN1A, CDKN2A, MET and HIF1A, link MITF to general cellular processes such as growth or survival. In this review, we provide an overview of the MITF-regulated genes. We pay special attention to the MITF target genes in melanocytes and raise questions about target specificity.
小眼畸形相关转录因子(MITF)最初通过对编码黑色素合成或黑素生成中涉及的三种酶的 TYROSINASE、TYRP1 和 DCT 基因的直接转录控制,被证明在黑素细胞分化中起关键作用。在 MITF 首次描述的 16 年后,已经描述了 40 多个直接的 MITF 靶基因。它们在黑素细胞、破骨细胞和肥大细胞的特异性功能中发挥关键作用。此外,MITF 靶基因,如 BCL2、CDK2、CDKN1A、CDKN2A、MET 和 HIF1A,将 MITF 与生长或存活等一般细胞过程联系起来。在这篇综述中,我们概述了 MITF 调节的基因。我们特别关注黑素细胞中的 MITF 靶基因,并提出了关于靶基因特异性的问题。