A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK

被引:15
作者
Foster, JW
Schafer, AJ
Critcher, R
Spillett, DJ
Feakes, RW
Walter, MA
DominguezSteglich, M
Guioli, S
Brook, JD
Goodfellow, PN
机构
[1] UNIV NOTTINGHAM HOSP,QUEENS MED CTR,DEPT GENET,NOTTINGHAM NG7 2UH,ENGLAND
[2] UNIV ALBERTA,DEPT OPHTHALMOL,EDMONTON,AB,CANADA
基金
英国惠康基金;
关键词
D O I
10.1006/geno.1996.0182
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 whole genome radiation hybrid (WG-RH) map across a region of human chromosome 17q, from growth hormone (GH) to thymidine kinase (TK). A panel of 128 WG-RH hybrid cell lines generated by X-irradiation and fusion has been tested for the retention of 39 sequence-tagged site (STS) markers by the polymerase chain reaction. This genome mapping technique has allowed the integration of existing VNTR and microsatellite markers with additional new markers and existing STS markers previously mapped to this region by other means. The WG-RH map includes eight expressed sequence tag (EST) and three anonymous markers developed for this study, together with 23 anonymous microsatellites and five existing ESTs. Analysis of these data resulted in a high-density comprehensive map across this region of the genome. A subset of these markers has been used to produce a framework map consisting of 20 loci ordered with odds greater than 1000:1. The markers are of sufficient density to build a YAC contig across this region based on marker content. We have developed sequence tags for both ends of a 2.1-Mb YAC and mapped these using the WG-RH panel, allowing a direct comparison of cRay(6000) to physical distance. (C) 1996 Academic Press, Inc.
引用
收藏
页码:185 / 192
页数:8
相关论文
共 31 条
[1]   A PROGRESSIVE EARLY-ONSET CATARACT GENE MAPS TO HUMAN-CHROMOSOME 17Q24 [J].
ARMITAGE, MM ;
KIVLIN, JD ;
FERRELL, RE .
NATURE GENETICS, 1995, 9 (01) :37-40
[2]   AN 8TH LOCUS FOR AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA IS LINKED TO CHROMOSOME-17Q [J].
BARDIEN, S ;
EBENEZER, N ;
GREENBERG, J ;
INGLEHEARN, CF ;
BARTMANN, L ;
GOLIATH, R ;
BEIGHTON, P ;
RAMESAR, R ;
BHATTACHARYA, SS .
HUMAN MOLECULAR GENETICS, 1995, 4 (08) :1459-1462
[3]   MULTIPOINT ANALYSIS FOR RADIATION HYBRID MAPPING [J].
BOEHNKE, M .
ANNALS OF MEDICINE, 1992, 24 (05) :383-386
[4]   CONSTRUCTION AND REGIONAL LOCALIZATION OF CLONES FROM A NOTI LINKING LIBRARY FROM HUMAN CHROMOSOME-17Q [J].
BORROW, J ;
BLACK, DM ;
GODDARD, AD ;
YAGLE, MK ;
FRISCHAUF, AM ;
SOLOMON, E .
GENOMICS, 1991, 10 (02) :477-480
[5]   HUMAN GROWTH-HORMONE DNA-SEQUENCE AND MESSENGER-RNA STRUCTURE - POSSIBLE ALTERNATIVE SPLICING [J].
DENOTO, FM ;
MOORE, DD ;
GOODMAN, HM .
NUCLEIC ACIDS RESEARCH, 1981, 9 (15) :3719-3730
[6]  
ECCLES DM, 1992, ONCOGENE, V7, P2069
[7]   NUCLEOTIDE-SEQUENCE OF THE HUMAN GAMMA-CYTOSKELETAL ACTIN MESSENGER-RNA - ANOMALOUS EVOLUTION OF VERTEBRATE NONMUSCLE ACTIN GENES [J].
ERBA, HP ;
GUNNING, P ;
KEDES, L .
NUCLEIC ACIDS RESEARCH, 1986, 14 (13) :5275-5294
[8]  
FAIN PR, 1991, CYTOGENET CELL GENET, V60, P177
[9]   ISOLATION AND CHARACTERIZATION OF SOMATIC-CELL HYBRIDS WITH BREAKPOINTS SPANNING 17Q22-]Q24 [J].
FLEJTER, WL ;
WATKINS, M ;
ABEL, KJ ;
CHANDRASEKHARAPPA, SC ;
WEBER, BL ;
COLLINS, FS ;
GLOVER, TW .
CYTOGENETICS AND CELL GENETICS, 1993, 64 (3-4) :222-223
[10]   CAMPOMELIC DYSPLASIA AND AUTOSOMAL SEX REVERSAL CAUSED BY MUTATIONS IN AN SRY-RELATED GENE [J].
FOSTER, JW ;
DOMINGUEZSTEGLICH, MA ;
GUIOLI, S ;
KWOK, C ;
WELLER, PA ;
STEVANOVIC, M ;
WEISSENBACH, J ;
MANSOUR, S ;
YOUNG, ID ;
GOODFELLOW, PN ;
BROOK, JD ;
SCHAFER, AJ .
NATURE, 1994, 372 (6506) :525-530