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小鼠小眼畸形蛋白的人类同源物对黑素细胞特异性基因的转录激活作用。

Transcriptional activation of the melanocyte-specific genes by the human homolog of the mouse Microphthalmia protein.

作者信息

Yasumoto K, Mahalingam H, Suzuki H, Yoshizawa M, Yokoyama K

机构信息

Department of Applied Physiology and Molecular Biology, Tohoku University School of Medicine.

出版信息

J Biochem. 1995 Nov;118(5):874-81. doi: 10.1093/jb/118.5.874.

Abstract

Mi protein encoded at the mouse microphthalmia (mi) locus is a transcription factor with a basic helix-loop-helix/leucine zipper structure. To assess the function of the human homolog of Mi protein, termed microphthalmia-associated transcription factor (MITF), we analyzed the effects of MITF on the promoter function of the mouse tyrosinase and tyrosinase-related protein 1 (TRP-1) genes. These two gene promoters are able to direct transcription preferentially in melanin-producing cells, and an enhancer element M box of 11 bp, containing a CATGTG motif, is conserved in both promoters. By transient expression assays, we have localized the cis-acting element of the tyrosinase gene responsible for pigment cell-specific expression to the proximal 82-bp region, which contains a CATGTG motif (positions -12 to -7) but lacks the M box (positions -107 to -97). We also provide evidence that the 82-bp region and the M box are involved in the transactivation of the tyrosinase promoter by MITF and that the M box is bound by MITF in vitro. Furthermore, MITF activated the TRP-1 gene promoter possibly through the M box (positions -44 to -34). These results suggest that MITF is a common factor regulating transcription of the pigment cell-specific genes.

摘要

在小鼠小眼畸形(mi)基因座编码的Mi蛋白是一种具有碱性螺旋-环-螺旋/亮氨酸拉链结构的转录因子。为了评估Mi蛋白的人类同源物小眼畸形相关转录因子(MITF)的功能,我们分析了MITF对小鼠酪氨酸酶和酪氨酸酶相关蛋白1(TRP-1)基因启动子功能的影响。这两个基因启动子能够优先在产生黑色素的细胞中指导转录,并且一个包含CATGTG基序的11bp增强子元件M盒在两个启动子中都是保守的。通过瞬时表达分析,我们已将负责色素细胞特异性表达的酪氨酸酶基因的顺式作用元件定位到近端82bp区域,该区域包含一个CATGTG基序(位置-12至-7)但缺少M盒(位置-107至-97)。我们还提供证据表明,82bp区域和M盒参与了MITF对酪氨酸酶启动子的反式激活,并且M盒在体外与MITF结合。此外,MITF可能通过M盒(位置-44至-34)激活TRP-1基因启动子。这些结果表明,MITF是调节色素细胞特异性基因转录的一个共同因子。

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