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Genetic Variants of IL-13 and IL-4 in the Korean Population: Polymorphisms, Haplotypes and Linkage Disequilibrium  

Ryu, Ha-Jung (National Genome Research Institute, National Institute of Health)
Jung, Ho-Youl (National Genome Research Institute, National Institute of Health)
Park, Jung-Sun (National Genome Research Institute, National Institute of Health)
Kim, Jun-Woo (National Genome Research Institute, National Institute of Health)
Kim, Hyung-Tae (Macrogen Co. World Meridian Venture Center)
Park, Choon-Sik (Genome Research Center for Allergy and Respiratory Diseases, Soonchunhyang University Hospital)
Han, Bok-Ghee (National Genome Research Institute, National Institute of Health)
Koh, In-Song (National Genome Research Institute, National Institute of Health)
Park, Chan (National Genome Research Institute, National Institute of Health)
Kimm, Ku-Chan (National Genome Research Institute, National Institute of Health)
Oh, Berm-Seok (National Genome Research Institute, National Institute of Health)
Lee, Jong-Keuk (National Genome Research Institute, National Institute of Health)
Abstract
Asthma is an inflammatory airways disease characterized by bronchial hyperresponsiveness and airways obstruction, which results from a complex interaction of genetic and environmental factors. Interleukin (IL)-13 and IL-4 are important in IgE synthesis and allergic inflammation, therefore genes encoding IL-13 and IL-4 are candidates for predisposition to asthma. In the present study, we screened single-nucleotide polymorphisms (SNPs) in IL-13 and IL-4 and examined whether they are risk factors for asthma. We resequenced all exons and the promoter region in 12 asthma patients and 12 normal controls, and identified 18 SNPs including 2 novel SNPs. The linkage disequilibrium(LD) pattern was evaluated with 16 common SNPs, and haplotypes were also estimated within the block. Although IL-13 and IL-4 are localized within 27 kb on chromosome 5q31 and share many biological profiles, this region was partitioned into 2 blocks. One SNP and three SNPs were determined as haplotype-taggingSNPs (htSNPs) within IL-13 and IL-4 haplotype-block, respectively. No significant associations were observed between any of the SNPs or haplotypes and development of asthma in small number of Korean subjects. However, the genetic variants of IL-13 and IL-4 would provide valuable strategies for the genotyping studies in large population.
Keywords
Asthma; Haplotype; IL-4; IL-13; Linkage Disequilibrium;
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