Cloning and characterization of a novel member of the human mad gene family (MADH6)

被引:48
作者
Watanabe, TK
Suzuki, M
Omori, Y
Hishigaki, H
Horie, M
Kanemoto, N
Fujiwara, T
Nakamura, Y
Takahashi, E
机构
[1] UNIV TOKYO,INST MED SCI,CTR HUMAN GENOME,MINATO KU,TOKYO 108,JAPAN
[2] UNIV TOKYO,MOL MED LAB,MINATO KU,TOKYO 108,JAPAN
[3] UNIV TOKYO,MOL MED LAB,MINATO KU,TOKYO 108,JAPAN
关键词
D O I
10.1006/geno.1997.4753
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
MAD (mothers against decapentaplegic)-related proteins (MADRs) are intracellular components that play critical roles in signal-transduction pathways involving the transforming growth factor beta (TGF beta) superfamily, Some Mad genes are candidates for tumor-suppressor functions, From a human fetal brain cDNA library we have isolated a novel Mad-related gene. Two alternatively transcribed mRNAs encode deduced 430- and 467-amino-acid peptides that showed high levels of similarity to MADR1/Smad1/hMAD1 (about 80% identity at the amino acid level), This gene, which we designated. MADH6, resides on 13q12-q14 between BRCA2 and RE, a region that frequently displays loss of heterozygosity in breast, liver, and prostate cancers. (C) 1997 Academic Press.
引用
收藏
页码:446 / 451
页数:6
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