Cloning and sequencing full-length HLA-B and -C genes

被引:34
作者
Cox, ST
McWhinnie, AJ
Robinson, J
Marsh, SGE
Parham, P
Madrigal, JA
Little, AM
机构
[1] Royal Free Hosp, Anthony Nolan Res Inst, London NW3 2QG, England
[2] Royal Free Hosp, Dept Haematol, London NW3 2QG, England
[3] Stanford Univ, Sch Med, Dept Biol Struct, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[5] Univ London Imperial Coll Sci Technol & Med, Sch Med, London, England
来源
TISSUE ANTIGENS | 2003年 / 61卷 / 01期
关键词
HLA; genomic; sequence;
D O I
10.1034/j.1399-0039.2003.610103.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Currently most available HLA-A, -B and -C DNA sequences cover exons 2 and 3 with a limited number extending to include other exons and introns. We have developed a method for the accurate determination of full-length genomic DNA sequences for HLA-A, -B and -C alleles. The method involves cloning of PCR amplified full-length HLA genes to separate alleles at heterozygous loci. The approach avoids any ambiguities from sequencing heterozygous PCR products directly and also avoids ambiguities from sequencing overlapping PCR products to achieve full-length sequence. To date we have sequenced full-length genomic sequences from representatives of all the major HLA-B and -C allele groups.
引用
收藏
页码:20 / 48
页数:29
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