High resolution HLA-DRB1 identification of a Caucasian population

被引:27
作者
Williams, F
Meenagh, A
Single, R
McNally, M
Kelly, P
Nelson, MP
Meyer, D
Lancaster, A
Thomson, G
Middleton, D
机构
[1] City Hosp, No Ireland Reg Histocompatibil & Immunogenet Lab, Belfast BT9 7TS, Antrim, North Ireland
[2] Univ Vermont, Dept Med Biostat, Burlington, VT USA
[3] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
[4] Queens Univ Belfast, Belfast, Antrim, North Ireland
[5] Univ Ulster, Coleraine BT52 1SA, Londonderry, North Ireland
关键词
HLA-DRB1; high resolution; sequence-specific oligonucleotide probes;
D O I
10.1016/j.humimm.2003.10.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Polymerase chain reaction-sequence-specific oligonucleotide probes typing methods have been applied to 1000 individuals from the Northern Ireland population to give human leuckocyte antigen DRB1 (HLA-DRB1) allele assignment. HLA-DRB1 allele frequencies and four-locus haplotypes (A/B/C/DR) for this Caucasian population, based on HLA class I and class II allele assignment, are now presented. No significant deviations from Hardy-Weinberg proportions were observed. The HLA-C locus exhibited marginal evidence of selection (p < 0.03, uncorrected one-sided test) in the direction of balancing selection; the HLA-A, -B, and -DRB1 allele frequency distributions were compatible with expectations under a neutral model (which does not mean that selection is not operating). Evidence for selection was seen on haplotypes HLA-A*010101-B*0801DRB1*030101 and HLA-A*290201-B*440301-DRB1*070101 based on their patterns of linkage disequilibrium.
引用
收藏
页码:66 / 77
页数:12
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