High-resolution integrated map encompassing the breast cancer loss of heterozygosity region on human chromosome 16q22.1

被引:15
作者
Frengen, E
Rocca-Serra, P
Shaposhnikov, S
Taine, L
Thorsen, J
Bepoldin, C
Krekling, M
Lafon, D
Aas, KK
Abd El Monéim, A
Johansen, H
Longy, M
Prydz, H
Dorion-Bonnet, F
机构
[1] Univ Oslo, Biotechnol Ctr Oslo, N-0349 Oslo, Norway
[2] Inst Bergonie, Lab Genet Mol EA515, Bordeaux, France
[3] Ctr Hosp Univ Pellegrin, Genet Lab, Bordeaux, France
关键词
D O I
10.1006/geno.2000.6389
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
Loss of heterozygosity (LOH) on the long arm of human chromosome 16 is a common genetic alteration observed in both invasive ductal and invasive lobular breast carcinomas. We have generated a high resolution integrated map encompassing the smallest region of LOH overlap within chromosome 16q22.1 (SRO2). Southern hybridization experiments using more than 140 probes resulted in the assembly of 152 bacterial large-insert clones into a 2.8-Mb contig covering SRO2. The structure of the contig was verified by long-range mapping using total human genomic DNA, and the contig orientation was determined by fluorescence in situ hybridization. A total of 68 transcripts have been identified in the map. One of the genes residing within SRO2 is the E-cadherin gene, CDH1, which has previously been shown to be mutated in lobular breast carcinomas, resulting in loss of E-cadherin expression. In most cases of ductal carcinoma, which is the major mammary cancer type, E-cadherin is normally expressed, suggesting that other genes within 16q22.1 are involved in the development of this tumor subtype. The high-resolution map presented in this study provides a valuable resource for identification of tumor suppressor genes expected to be involved in the etiology of breast carcinomas. (C) 2000 Academic Press.
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页码:273 / 285
页数:13
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