| Literature DB >> 11169252 |
M Komatsu-Wakui1, K Tokunaga, Y Ishikawa, C Leelayuwat, K Kashiwase, H Tanaka, S Moriyama, F Nakajima, M H Park, G J Jia, N O Chimge, E W Sideltseva, T Juji.
Abstract
Stress-inducible MICA (MHC class I chain-related A) is known to bind to NKG2D, which is one of the natural killer (NK) cell receptors, and plays a role in immune surveillance. We have reported that a MICA-MICB null haplotype is in linkage disequilibrium with HLA-B*4801 in the Japanese population. In the haplotype, an approximately 100-kb deletion, including the entire MICA gene, was observed and MICB possessed a premature stop codon. In this study, a multiplex polymerase chain reaction (PCR) method was developed for detecting the MICA deletion. MICB alleles were typed by PCR-single-strand conformation polymorphism (SSCP) method and direct sequencing. The frequency of the MICA-MICB null haplotype was 3.7% on the average, and was strongly associated with HLA-B48 in seven East Asian populations. It was presumed that the stop codon of MICB gene generated after the large-scale deletion. The wide distribution of the null haplotype at polymorphic frequencies suggests that the haplotype has been conservatively maintained because of some selective advantage.Entities:
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Year: 2001 PMID: 11169252 DOI: 10.1034/j.1399-0039.2001.057001001.x
Source DB: PubMed Journal: Tissue Antigens ISSN: 0001-2815