TY - JOUR
T1 - Structural organization of the human microphthalmia-associated transcription factor gene containing four alternative promoters
AU - Udono, Tetsuo
AU - Yasumoto, Ken Ichi
AU - Takeda, Kazuhisa
AU - Amae, Shintaro
AU - Watanabe, Ken Ichi
AU - Saito, Hideo
AU - Fuse, Nobuo
AU - Tachibana, Masayoshi
AU - Takahashi, Kazuhiro
AU - Tamai, Makoto
AU - Shibahara, Shigeki
PY - 2000/4/25
Y1 - 2000/4/25
N2 - 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. Copyright (C) 2000 Elsevier Science B.V.
AB - 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. Copyright (C) 2000 Elsevier Science B.V.
KW - Auditory-pigmentary syndrome
KW - Cell differentiation
KW - Gene transcription
KW - Melanocyte
KW - Retinal pigment epithelium
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U2 - 10.1016/S0167-4781(00)00051-8
DO - 10.1016/S0167-4781(00)00051-8
M3 - Article
C2 - 10760582
AN - SCOPUS:0000841754
SN - 0167-4781
VL - 1491
SP - 205
EP - 219
JO - BBA - Gene Structure and Expression
JF - BBA - Gene Structure and Expression
IS - 1-3
ER -