EPIDERMOLYTIC PALMOPLANTAR KERATODERMA COSEGREGATES WITH A KERATIN-9 MUTATION IN A PEDIGREE WITH BREAST AND OVARIAN-CANCER

被引:110
作者
TORCHARD, D
BLANCHETBARDON, C
SEROVA, O
LANGBEIN, L
NAROD, S
JANIN, N
GOGUEL, AF
BERNHEIM, A
FRANKE, WW
LENOIR, GM
FEUNTEUN, J
机构
[1] INST GUSTAVE ROUSSY,ONCOL MOLEC LAB,CNRS,URA 1158,F-94805 VILLEJUIF,FRANCE
[2] INST GUSTAVE ROUSSY,CYTOGENET & GENET ONCOL LAB,F-94805 VILLEJUIF,FRANCE
[3] HOP ST LOUIS,MALAD CUTANEES CLIN,F-75010 PARIS,FRANCE
[4] INT AGCY RES CANC,F-69372 LYON,FRANCE
[5] GERMAN CANC RES CTR,W-6900 HEIDELBERG 1,GERMANY
[6] MCGILL UNIV,CTR HUMAN GENET,MONTREAL H3A 2T5,QUEBEC,CANADA
[7] MCGILL UNIV,DEPT MED,MONTREAL H3A 2T5,QUEBEC,CANADA
[8] MCGILL UNIV,DEPT ONCOL,MONTREAL H3A 2T5,QUEBEC,CANADA
[9] INST GUSTAVE ROUSSY,DEPT MED,F-94805 VILLEJUIF,FRANCE
关键词
D O I
10.1038/ng0194-106
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Epidermolytic palmoplantar keratosis (EPPK) cosegregates with breast and ovarian cancers in a large French pedigree, raising the possibility that a single genetic mutation might cause these conditions and offering a potential lead to the identification of a hereditary breast/ovarian cancer gene. We have performed linkage analysis and show that the EPPK locus lies on the long arm of chromosome 17 near the type I keratin gene cluster and the proposed breast cancer gene (BRCA1). The type I keratin 9 gene has been partially sequenced in four affected individuals. A single base mutation within the rod domain of the protein cosegregates with EPPK in all affected individuals tested. Although inheritance of this mutation is likely responsible for EPPK, it is unlikely to be the cause of the breast and ovarian cancer.
引用
收藏
页码:106 / 110
页数:5
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