Estimation of the 6-digit level allele and haplotype frequencies of HLA-A, -B, and -C in Koreans using ambiguity-solving DNA typing
- Authors
- Jun, J. -H.; Hwang, K.; Kim, S. -K.; Oh, H. -B.; Cho, M. -C.; Lee, K. -J.
- Issue Date
- Sep-2014
- Publisher
- WILEY
- Keywords
- allele; ambiguity; haplotype; human leukocyte antigen; Korean; six-digit
- Citation
- TISSUE ANTIGENS, v.84, no.3, pp 277 - 284
- Pages
- 8
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- TISSUE ANTIGENS
- Volume
- 84
- Number
- 3
- Start Page
- 277
- End Page
- 284
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/18800
- DOI
- 10.1111/tan.12368
- ISSN
- 0001-2815
1399-0039
- Abstract
- Because Korean society is fast becoming multi-ethnic, the determination of ambiguous human leukocyte antigen (HLA) types using HLA allele frequencies is becoming less applicable. In this study, we focused on the development of new technical methods to directly resolve the ambiguities arising from HLA genotyping. One hundred and fifty unrelated healthy Korean adults were included in this study. All alleles from each HLA locus were first divided into 2-4 groups, with each group amplified in a single PCR tube (multi-group-specific amplification, MGSA). To resolve phase ambiguities, some allele groups were also amplified separately in small group-specific amplification (SGSA) tubes. In order to then resolve incomplete sequence ambiguities, primers for MGSA and SGSA were initially designed to cover additional exons. If needed, a heterozygous ambiguity resolving primer (HARP) or sequence specific primer (SSP) was also used. When MGSA and SGSA methods were applied, the rate of phase ambiguity was greatly reduced to an average of 6%(1.3% in HLA-A, 15.7% in -B, and 2.0% in -C). Additional HARP and SSP methods could resolve all the phase ambiguities. Using our proposed method, we also detected three alleles that have not been previously reported in Korea, C*04: 82, C*07: 18, and C*08: 22, and report 6-digit level HLA allele and haplotype frequencies among Koreans. In conclusion, the use of MGSA/SGSA for the initial amplification step is a cost-effective method facilitating timely and accurate reporting, given the continuing increase in the ethnic diversity of the Korean population. The MGSA described here can be applicable to various populations and thus could be shared by the majority of HLA typing laboratories. However, efforts to solve HLA ambiguity should continue, because SGSA, HARPs and SSPs would be specific to a particular population.
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