| Literature DB >> 20087405 |
Pei-Song Gao1, Kenichi Shimizu, Audrey V Grant, Nicholas Rafaels, Lin-Fu Zhou, Sherry A Hudson, Satoshi Konno, Nives Zimmermann, Maria I Araujo, Eduardo V Ponte, Alvaro A Cruz, Masaharu Nishimura, Song-Nan Su, Nobuyuki Hizawa, Terry H Beaty, Rasika A Mathias, Marc E Rothenberg, Kathleen C Barnes, Bruce S Bochner.
Abstract
Sialic acid-binding immunoglobulin-like lectin-8 (Siglec-8) promotes the apoptosis of eosinophils and inhibits FcvarepsilonRI-dependent mediator release from mast cells. We investigated the genetic association between sequence variants in Siglec-8 and diagnosis of asthma, total levels of serum IgE (tIgE), and diagnosis of eosinophilic esophagitis (EE) in diverse populations. The effect of sequence variants on Siglec-8 glycan ligand-binding activity was also examined. Significant association with asthma was observed for SNP rs36498 (odds ratios (OR), 0.69, P=8.8 x 10(-5)) among African Americans and for SNP rs10409962 (Ser/Pro) in the Japanese population (OR, 0.69, P=0.019). Supporting this finding, we observed association between SNP rs36498 and current asthma among Brazilian families (P=0.013). Significant association with tIgE was observed for SNP rs6509541 among African Americans (P=0.016), and replicated among the Brazilian families (P=0.02). In contrast, no association was observed with EE in Caucasians. By using a synthetic polymer decorated with 6'-sulfo-sLe(x), a known Siglec-8 glycan ligand, we did not find any differences between the ligand-binding activity of HEK293 cells stably transfected with the rs10409962 risk allele or the WT allele. However, our association results suggest that the Siglec8 gene may be a susceptibility locus for asthma.Entities:
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Year: 2010 PMID: 20087405 PMCID: PMC2987348 DOI: 10.1038/ejhg.2009.239
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 4.246