共 16 条
CLONING, CHARACTERIZATION AND CHROMOSOMAL ASSIGNMENT OF THE HUMAN GENES HOMOLOGOUS TO YEAST PMS1, A MEMBER OF MISMATCH REPAIR GENES
被引:61
作者:

HORII, A
论文数: 0 引用数: 0
h-index: 0
机构: Department of Biochemistry, Cancer Institute, Toshima-ku, Tokyo 170

HAN, HJ
论文数: 0 引用数: 0
h-index: 0
机构: Department of Biochemistry, Cancer Institute, Toshima-ku, Tokyo 170

SASAKI, S
论文数: 0 引用数: 0
h-index: 0
机构: Department of Biochemistry, Cancer Institute, Toshima-ku, Tokyo 170

SHIMADA, M
论文数: 0 引用数: 0
h-index: 0
机构: Department of Biochemistry, Cancer Institute, Toshima-ku, Tokyo 170

NAKAMURA, Y
论文数: 0 引用数: 0
h-index: 0
机构: Department of Biochemistry, Cancer Institute, Toshima-ku, Tokyo 170
机构:
[1] Department of Biochemistry, Cancer Institute, Toshima-ku, Tokyo 170
关键词:
D O I:
10.1006/bbrc.1994.2598
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:
Mutations in genes associated with the DNA mismatch repair system were considered to play important roles in predisposition to cancer, since hMSH2 and hMLH1, human homologues of yeast MSH2 and MLH1 as well as bacterial mutS and mutL genes, were found to be involved in hereditary nonpolyposis colorectal cancer(HNPCC). In addition, yeast PMS1 that is homologous to bacterial mutL and hexB, has also been proven to be related to the DNA mismatch repair system. As the first step to understand whether human homologue of the yeast PMS1 gene is associated with genetic predisposition to cancer, we have isolated and analyzed human counterpart of yeast PMS1 genes. DNA sequencing analyses indicated that human PMS genes constituted a multiple gene family and that some of the family members have been mapped to chromosomal bands 7q11.23 and 7q22 by fluorescent in situ hybridization. (C) 1994 Academic Press, Inc.
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页码:1257 / 1264
页数:8
相关论文
共 16 条
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PELTOMAKI, P
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AALTONEN, LA
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FOURNIER, REK
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TODD, S
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NAYLOR, SL
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TRENT, JM
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