A RADIATION HYBRID MAP OF HUMAN CHROMOSOME-11Q22-Q23 CONTAINING THE ATAXIA-TELANGIECTASIA DISEASE LOCUS

被引:33
作者
RICHARD, CW
COX, DR
KAPP, L
MURNANE, J
CORNELIS, F
JULIER, C
LATHROP, GM
JAMES, MR
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT PSYCHIAT,SAN FRANCISCO,CA 94117
[2] UNIV CALIF SAN FRANCISCO,DEPT BIOCHEM & BIOPHYS,SAN FRANCISCO,CA 94117
[3] UNIV CALIF SAN FRANCISCO,DEPT RADIOBIOL & ENVIRONM HLTH,SAN FRANCISCO,CA 94117
[4] INSERM,U358,F-75005 PARIS,FRANCE
[5] CTR ETUD POLYMORPHISME HUMAIN,PARIS,FRANCE
关键词
D O I
10.1006/geno.1993.1275
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
We describe a high-resolution radiation hybrid map of human chromosome 11q22-q23 containing the ataxia-telangiectasia (AT) disease gene loci. The order and intermarker distances of 32 chromosome 11q22-q23 markers were determined by a multipoint maximum likelihood method of analysis of the cosegregation of markers in 100 radiation hybrids. The radiation hybrid map of polymorphic loci was consistent with genetic linkage maps of common markers. Several genes, including αB-crystallin, adrenal ferrodoxin, CBL2, collagenase, dopamine receptor type 2, neural cell adhesion molecule, progesterone receptor, and stromelysins 1 and 2, were placed in relation to previously ordered, genetically mapped polymorphic loci. Five new markers (αB-crystallin, adrenal ferrodoxin, CJ52.114, CJ52.3, and D11S535) were ordered within the current published flanking markers for the AT group A and group C disease loci. A candidate AT group D gene (ATDC) identified by Kapp et al. (1992, Am. J. Hum. Genet. 51: 45-54) was mapped telomeric to THY1, outside the flanking markers identified by multipoint linkage analysis for the major AT locus. © 1993 Academic Press, Inc.
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页码:1 / 5
页数:5
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