Mitf-D, a newly identified isoform, expressed in the retinal pigment epithelium and monocyte-lineage cells affected by Mitf mutations

被引:71
作者
Takeda, K
Yasumoto, K
Kawaguchi, N
Udono, T
Watanabe, K
Saito, H
Takahashi, K
Noda, M
Shibahara, S
机构
[1] Tohoku Univ, Sch Med, Dept Mol Biol & Appl Physiol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tokyo Med & Dent Univ, Inst Med Res, Dept Mol Pharmacol, Chiyoda Ku, Tokyo 1010062, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2002年 / 1574卷 / 01期
关键词
cell differentiation; macrophage; Mitf; osteoclast; retinal pigment epithelium; transcription;
D O I
10.1016/S0167-4781(01)00339-6
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) regulates the differentiation of melanocytes, optic cup-derived retinal pigment epithelium (RPE), and some types of bone marrow-derived cells. Mitf consists of at least five isoforms with different N-termini, each of which is encoded by a separate exon 1. Here we identified a novel isoform, termed mouse Mitf-D/human MITF-D, that is expressed in RPE, macrophages, and osteoclasts affected by the Mitf mutations, but not expressed in other Mitf target cells, including melanocyte-lineage cells and natural killer cells. The initiation Met of MITF-D is located in the downstream domain (Blb domain) that is shared by other MITF isoforms. The 5'-untranslated region of MITF-D mRNA is encoded by the newly identified first exon of the MITF gene, termed exon ID, which is located 3 kb upstream of the exon encoding the Blb domain. Thus, the MITF gene generates multiple isoforms with different expression patterns by using the alternative promoters in a cell-dependent manner. thereby providing the molecular basis for the phenotypic variability seen in the MITF/Mitf mutants. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:15 / 23
页数:9
相关论文
共 37 条
[31]   Structural organization of the human microphthalmia-associated transcription factor gene containing four alternative promoters [J].
Udono, T ;
Yasumoto, K ;
Takeda, K ;
Amae, S ;
Watanabe, K ;
Saito, H ;
Fuse, N ;
Tachibana, M ;
Takahashi, K ;
Tamai, M ;
Shibahara, S .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2000, 1491 (1-3) :205-219
[32]   Age-resolving osteopetrosis: A rat model implicating microphthalmia and the related transcription factor TFE3 [J].
Weilbaecher, KN ;
Hershey, CL ;
Takemoto, CM ;
Horstmann, MA ;
Hemesath, TJ ;
Tashjian, AH ;
Fisher, DE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (05) :775-785
[33]   An L1 element intronic insertion in the black-eyed white (Mitfmi-bw) gene:: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness [J].
Yajima, I ;
Sato, S ;
Kimura, T ;
Yasumoto, K ;
Shibahara, S ;
Goding, CR ;
Yamamoto, H .
HUMAN MOLECULAR GENETICS, 1999, 8 (08) :1431-1441
[34]   TRANSCRIPTIONAL ACTIVATION OF THE MELANOCYTE-SPECIFIC GENES BY THE HUMAN HOMOLOG OF THE MOUSE MICROPHTHALMIA PROTEIN [J].
YASUMOTO, K ;
MAHALINGAM, H ;
SUZUKI, H ;
YOSHIZAWA, M ;
YOKOYAMA, K ;
SHIBAHARA, S .
JOURNAL OF BIOCHEMISTRY, 1995, 118 (05) :874-881
[35]   A big gene linked to small eyes encodes multiple Mitf isoforms: Many promoters make light work [J].
Yasumoto, K ;
Amae, S ;
Udono, T ;
Fuse, N ;
Takeda, K ;
Shibahara, S .
PIGMENT CELL RESEARCH, 1998, 11 (06) :329-336
[36]  
Yasumoto K, 1997, J BIOL CHEM, V272, P503
[37]   MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR AS A REGULATOR FOR MELANOCYTE-SPECIFIC TRANSCRIPTION OF THE HUMAN TYROSINASE GENE [J].
YASUMOTO, KI ;
YOKOYAMA, K ;
SHIBATA, K ;
TOMITA, Y ;
SHIBAHARA, S .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) :8058-8070