Structural organization of the human microphthalmia-associated transcription factor gene containing four alternative promoters

被引:110
作者
Udono, T
Yasumoto, K
Takeda, K
Amae, S
Watanabe, K
Saito, H
Fuse, N
Tachibana, M
Takahashi, K
Tamai, M
Shibahara, S [1 ]
机构
[1] Tohoku Univ, Sch Med, Dept Mol Biol & Appl Physiol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Sch Med, Dept Ophthalmol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[3] Saitama Canc Ctr, Res Inst, Moroyama, Saitama 3620806, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2000年 / 1491卷 / 1-3期
关键词
auditory-pigmentary syndrome; cell differentiation; gene transcription; melanocyte; retinal pigment epithelium;
D O I
10.1016/S0167-4781(00)00051-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microphthalmia-associated transcription factor (MITF) affects the development of many types of cells, including melanocytes and retinal pigment epithelium (RPE). MITF consists of at least three isoforms, MITF-A, MITF-H and MITF-M, differing at their amino-termini and expression patterns. Here, we characterize the structural organization of the human MITF gene. The gene contains at least four isoform-specific first exons, exons 1A, 1H, 1B and 1M in the 5' to 3' direction, each of which encodes the unique amino-terminus of a given isoform, including newly identified MITF-B. The 5'-flanking regions of these isoform-specific exons are termed promoters A, H, B and M, respectively, which showed different promoter activities, as judged by transient transfection assay. Promoter A directs the expression of a reporter gene in RPE, cervical cancer and melanoma cells, whereas promoter M is functional only in melanoma cells. Promoter H showed the significant activity in RPE and cervical cancer cells but not in melanoma cells. In contrast, the 1.7 kb 5'-flanking region of exon 1B showed no noticeable promoter activity in these cell lines. Therefore, alternative promoters provide the MITF gene with the diversity in transcriptional regulation and the capability of generating structurally different protein isoforms. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:205 / 219
页数:15
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