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PMID: 15853898 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Allelic and haplotypic diversity of HLA-A, -B, -C, -DRB1, and -DQB1 genes in the Korean population.

Tissue antigens ·Vol. 65 ·No. 5 ·2005-05-00 ·Pages 437-47

Lee KW, Oh DH, Lee C, Yang SY

Abstract

High-resolution human leukocyte antigen (HLA) typing exposes the unique patterns of HLA allele and haplotype frequencies in each population. In this study, HLA-A, -B, -C, -DRB1, and -DQB1 genotypes were analyzed in 485 apparently unrelated healthy Korean individuals. A total of 20 HLA-A, 43 HLA-B, 21 HLA-C, 31 HLA-DRB1, and 14 HLA-DQB1 alleles were identified. Eleven alleles (A*0201, A*1101, A*2402, A*3303, B*1501, Cw*0102, Cw*0302, Cw*0303, DQB1*0301, DQB1*0302, and DQB1*0303) were found in more than 10% of the population. In each serologic group, a maximum of three alleles were found with several exceptions (A2, B62, DR4, DR14, and DQ6). In each serologic group exhibiting multiple alleles, two major alleles were present at 62-96% (i.e. A*0201 and A*0206 comprise 85% of A2-positive alleles). Multiple-locus haplotypes estimated by the maximum likelihood method revealed 51 A-C, 43 C-B, 52 B-DRB1, 34 DRB1-DQB1, 48 A-C-B, 42 C-B-DRB1, 46 B-DRB1-DQB1, and 30 A-C-B-DRB1-DQB1 haplotypes with frequencies of more than 0.5%. In spite of their high polymorphism in B and DRB1, identification of relatively small numbers of two-locus (B-C and DRB1-DQB1) haplotypes suggested strong associations of those two loci, respectively. Five-locus haplotypes defined by high-resolution DNA typing correlated well with previously identified serology-based haplotypes in the population. The five most frequent haplotypes were: A*3303-Cw*1403-B*4403-DRB1*1302-DQB1*0604 (4.2%), A*3303-Cw*0701/6-B*4403-DRB1*0701-DQB1*0201/2 (3.0%), A*3303-Cw*0302-B*5801-DRB1*1302-DQB1*0609 (3.0%), A*2402-Cw*0702-B*0702-DRB1*0101-DQB1*0501 (2.9%), and A*3001-Cw*0602-B*1302-DRB1*0701-DQB1*0201/2 (2.7%). Several sets of allele level haplotypes that could not be discriminated by routine HLA-A, -B, and -DRB1 low-resolution typing originated from allelic diversity of A2, B61, DR4, and DR8 serologic groups. Information obtained in this study will be useful for medical and forensic applications as well as in anthropology.

MeSH Terms
Alleles Asians/genetics Ethnicity/genetics Gene Frequency Genotype HLA-A Antigens/genetics HLA-B Antigens/genetics HLA-C Antigens/genetics HLA-DQ Antigens/genetics HLA-DQ beta-Chains HLA-DR Antigens/genetics HLA-DRB1 Chains Haplotypes/genetics Humans Japan/ethnology Korea Likelihood Functions Major Histocompatibility Complex/genetics Polymerase Chain Reaction
Chemicals
HLA-A Antigens HLA-B Antigens HLA-C Antigens HLA-DQ Antigens HLA-DQ beta-Chains HLA-DQB1 antigen HLA-DR Antigens HLA-DRB1 Chains
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lee K W
Hallym Institution for Genome Application, Hallym University, Sacred Heart Hospital, #896 Pyungchon-Dong, Dongan-Ku, Anyang, Kyungki-Do 431-070, Korea. [email protected]
Oh D H
Lee C
Yang S Y
Article Info
Journal
Tissue antigens
Abbr.
Tissue Antigens
ISSN
0001-2815
Published
2005-05-00
Pages
437-47
Language
English
Region
England
NLM ID
0331072
Subset
IM
Grants
NCI NIH HHS · P01 CA 23766 · United States
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