GENE-BASED SEQUENCE-TAGGED-SITES (STSS) AS THE BASIS FOR A HUMAN GENE MAP

被引:77
作者
BERRY, R
STEVENS, TJ
WALTER, NAR
WILCOX, AS
RUBANO, T
HOPKINS, JA
WEBER, J
GOOLD, R
SOARES, MB
SIKELA, JM
机构
[1] UNIV COLORADO,HLTH SCI CTR,DEPT PHARMACOL,DENVER,CO 80262
[2] UNIV COLORADO,HLTH SCI CTR,PROGRAM MOLEC BIOL,DENVER,CO 80262
[3] VET ADM SCHIZOPHRENIA CTR,DENVER,CO 80262
[4] MARSHFIELD MED RES FDN,MARSHFIELD,WI 54449
[5] STANFORD UNIV,CTR HUMAN GENOME MAPPING,STANFORD,CA 94305
[6] COLUMBIA UNIV COLL PHYS & SURG,DEPT PSYCHIAT,NEW YORK,NY 10032
[7] NEW YORK STATE PSYCHIAT INST & HOSP,NEW YORK,NY 10032
关键词
D O I
10.1038/ng0895-415
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Using our data set of 3,143 single pass sequences from human brain cDNA libraries, we have developed a strategy in which gene-based sequence-tagged-sites (STSs), derived from 3'untranslated regions of human cDNAs, are rapidly assigned to megabase-insert yeast artificial chromosomes and somatic cell hybrids to generate regional gene mapping data, Employing this approach, we have mapped 318 cDNAs, representing 308 human genes. Ninety-two of these mapped to regions implicated in human genetic diseases, identifying them as candidate genes. Extension of this strategy has the potential to result in virtually every human gene having, at its 3'end, its own associated STS, with each STS in turn specifying both a corresponding genomic clone and a specific regional location in the genome.
引用
收藏
页码:415 / 423
页数:9
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