PHYSICAL MAP ACROSS CHROMOSOME 11Q22-Q23 CONTAINING THE MAJOR LOCUS FOR ATAXIA-TELANGIECTASIA

被引:21
作者
AMBROSE, HJ
BYRD, PJ
MCCONVILLE, CM
COOPER, PR
STANKOVIC, T
RILEY, JH
SHILOH, Y
MCNAMARA, JO
FUKAO, T
TAYLOR, AMR
机构
[1] UNIV BIRMINGHAM,SCH MED,DEPT CANC STUDIES,CRC,BIRMINGHAM B15 2TJ,W MIDLANDS,ENGLAND
[2] ZENECA PHARMACEUT,MACCLESFIELD SK10 4GT,CHESHIRE,ENGLAND
[3] TEL AVIV UNIV,SACKLER SCH MED,DEPT HUMAN GENET,IL-69978 RAMAT AVIV,ISRAEL
[4] DUKE UNIV,MED CTR,DEPT VET AFFAIRS MED CTR,DURHAM,NC 27710
[5] GIFU UNIV,SCH MED,DEPT PEDIAT,GIFU 500,JAPAN
关键词
D O I
10.1006/geno.1994.1321
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 have constructed a long-range physical map for 12 markers, including genes for GRIA4, IL1BC, and ACAT, across 9 Mb of chromosome 11q22-q23 in the region of the major locus for ataxia-telangiectasia (A-T). The markers fall into proximal and distal groups with respect to the centromere. We have linked the proximal and distal groups by hybridization to a 2.7-Mb NotI fragment and a 4.6-Mb MluI fragment. The following locus order was obtained: centromere-CJ52.75-J12.1C2-Y11B11R-IL1BC-hbcDNA-GRIA4-CJ52.3-Y11B29L-ACAT-CJ52.193-J12.8-Y11B06R-telomere. We show that hbcDNA/GRIA4 and CJ52.3 are very closely linked to each end, respectively, of the 2.7-Mb NotI fragment, thereby fixing the position of the complete contig. Our results indicate that the gene for A-T is flanked by the markers GRIA4 and J12.8, which are no more than 3 Mb apart, on a 4.6-Mb MluI fragment. The physical map allows rapid positioning of markers, and this will facilitate the construction of a YAC contig across the region. (C) 1994 Academic Press, Inc.
引用
收藏
页码:612 / 619
页数:8
相关论文
共 25 条
[1]  
BRADBURY D, 1990, LEUKEMIA, V4, P44
[2]  
BYRD PJ, 1991, CYTOGENET CELL GENET, V58, P1956
[3]   MOLECULAR-CLONING OF THE INTERLEUKIN-1-BETA CONVERTING ENZYME [J].
CERRETTI, DP ;
KOZLOSKY, CJ ;
MOSLEY, B ;
NELSON, N ;
VANNESS, K ;
GREENSTREET, TA ;
MARCH, CJ ;
KRONHEIM, SR ;
DRUCK, T ;
CANNIZZARO, LA ;
HUEBNER, K ;
BLACK, RA .
SCIENCE, 1992, 256 (5053) :97-100
[4]   HUMAN GLOBIN GENE-EXPRESSION IN HYBRID 2S MEL X HUMAN FIBROBLAST CELLS [J].
CHIANG, YL ;
LEY, TJ ;
SANDERSHAIGH, L ;
ANDERSON, WF .
SOMATIC CELL AND MOLECULAR GENETICS, 1984, 10 (04) :399-407
[5]  
ESTROV Z, 1991, BLOOD, V78, P1476
[6]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[7]   THE ORDER AND ORIENTATION OF A CLUSTER OF METALLOPROTEINASE GENES, STROMELYSIN-2, COLLAGENASE, AND STROMELYSIN, TOGETHER WITH D11S385, ON CHROMOSOME-11Q22-Q23 [J].
FORMSTONE, CJ ;
BYRD, PJ ;
AMBROSE, HJ ;
RILEY, JH ;
HERNANDEZ, D ;
MCCONVILLE, CM ;
TAYLOR, AMR .
GENOMICS, 1993, 16 (01) :289-291
[8]   LOCALIZATION OF AN ATAXIA-TELANGIECTASIA GENE TO CHROMOSOME 11Q22-23 [J].
GATTI, RA ;
BERKEL, I ;
BODER, E ;
BRAEDT, G ;
CHARMLEY, P ;
CONCANNON, P ;
ERSOY, F ;
FOROUD, T ;
JASPERS, NGJ ;
LANGE, K ;
LATHROP, GM ;
LEPPERT, M ;
NAKAMURA, Y ;
OCONNELL, P ;
PATERSON, M ;
SALSER, W ;
SANAL, O ;
SILVER, J ;
SPARKES, RS ;
SUSI, E ;
WEEKS, DE ;
WEI, S ;
WHITE, R ;
YODER, F .
NATURE, 1988, 336 (6199) :577-580
[9]   A DETAILED GENETIC-MAP OF THE LONG ARM OF CHROMOSOME-11 [J].
JULIER, C ;
NAKAMURA, Y ;
LATHROP, M ;
OCONNELL, P ;
LEPPERT, M ;
LITT, M ;
MOHANDAS, T ;
LALOUEL, JM ;
WHITE, R .
GENOMICS, 1990, 7 (03) :335-345
[10]  
KUWAHARA T, 1992, HUM GENET, V90, P208