Takabatake Noriaki, Toriyama Sayumi, Takeishi Yasuchika, Shibata Yoko, Konta Tsuneo, Inoue Sumito, Abe Shuichi, Igarashi Akira, Tokairin Yoshikane, Ishii Miho, Koyano Satoru, Emi Mitsuru, Kato Takeo, Kawata Sumio, Kubota Isao
Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine, 2-2-2, Iida-Nishi, Yamagata 990-9585, Japan.
Biochem Biophys Res Commun. 2007 Dec 21;364(3):662-7. doi: 10.1016/j.bbrc.2007.10.068. Epub 2007 Oct 22.
The forced expiratory volume in the first second (FEV1.0)/the forced vital capacity (FVC) is an important index of a single forced expiration. Ectopic expression of the human olfactory receptor (OR) gene family in the lungs has suggested its potential involvement of respiratory physiology. We hypothesized that the individual variability of FEV1.0/FVC value may be attributed to the genetic variance of the OR gene family caused by the nonfunctioning SNPs (nSNPs). We conducted quantitative trait locus (QTL) analyses of population having the 7 OR gene nSNPs and FEV1.0/FVC values by ANOVA, in 2970 samples in the Yamagata Takahata cohort. We found significant association of one nSNP [rs10838851, OR, family 4, subfamily X, member 1 (OR4X1) gene, Tyr273Ter*] with FEV1.0/FVC (%) (P = 0.008). The FEV1.0/FVC value (%) of population having OR4X1 gene nSNP Ter*/Ter*, Ter*/Tyr, and Tyr/Tyr were 78.9 +/- 0.2, 78.2 +/- 0.2, and 77.7 +/- 0.4, respectively. Haplotype-based analysis of the OR4X1 gene with FEV1.0/FVC values demonstrated that two exclusive haplotypes [Hap-1/Hap-2 (frequency 0.669/0.330): SNP1 (rs7106648)T/A-SNP2 (rs871249)G/A-SNP3 (rs713325)G/A-SNP4 (rs10838851)A (Ter*)/T (Tyr)-SNP5 (rs4752923)G/A-SNP6 (rs960640)G/A] were significantly associated with FEV1.0/FVC values (global P = 0.005). These results suggest that OR4X1 may be one of the genes that contribute to the individual variability of FEV1.0/FVC value in pulmonary function test.
第一秒用力呼气量(FEV1.0)/用力肺活量(FVC)是单次用力呼气的一项重要指标。人类嗅觉受体(OR)基因家族在肺部的异位表达提示其可能参与呼吸生理过程。我们推测FEV1.0/FVC值的个体差异可能归因于无功能单核苷酸多态性(nSNP)导致的OR基因家族的遗传变异。我们通过方差分析对山形高畑队列中的2970个样本进行了具有7个OR基因nSNP和FEV1.0/FVC值的群体的数量性状位点(QTL)分析。我们发现一个nSNP [rs10838851,OR,第4家族,X亚家族,成员1(OR4X1)基因,Tyr273Ter*]与FEV1.0/FVC(%)显著相关(P = 0.008)。具有OR4X1基因nSNP Ter*/Ter*、Ter*/Tyr和Tyr/Tyr的群体的FEV1.0/FVC值(%)分别为78.9±0.2、78.2±0.2和77.7±0.4。基于单倍型的OR4X1基因与FEV1.0/FVC值的分析表明,两种排他性单倍型[Hap-1/Hap-2(频率0.669/0.330):SNP1(rs7106648)T/A-SNP2(rs871249)G/A-SNP3(rs713325)G/A-SNP4(rs10838851)A(Ter*)/T(Tyr)-SNP5(rs4752923)G/A-SNP6(rs960640)G/A]与FEV1.0/FVC值显著相关(总体P = 0.005)。这些结果表明,OR4X1可能是导致肺功能测试中FEV1.0/FVC值个体差异的基因之一。