Son Ho-Young, Sohn Seong-Wook, Im Sun-Hwa, Kim Hyun-Jin, Lee Mi Kyeong, Gombojav Bayasgalan, Kwon Hyouk-Soo, Park Daniel S, Kim Hyung-Lae, Min Kyung-Up, Sung Joohon, Seo Jeong-Sun, Kim Jong-Il
Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Department of Internal Medicine, Dongguk University Ilsan Hospital, Goyang, Republic of Korea.
PLoS One. 2015 Oct 2;10(10):e0139716. doi: 10.1371/journal.pone.0139716. eCollection 2015.
The spirometric measurement of pulmonary function by measuring the forced expiratory volume in one second (FEV1) is a heritable trait that reflects the physiological condition of the lung and airways. Genome-wide linkage and association studies have identified a number of genes and genetic loci associated with pulmonary function. However, limited numbers of studies have been reported for Asian populations. In this study, we aimed to investigate genetic evidence of pulmonary function in a population in northeast Asia. We conducted a family-based association test with 706 GENDISCAN study participants from 72 Mongolian families to determine candidate genetic determinants of pulmonary function. For the replication, we chose seven candidate single nucleotide polymorphisms (SNPs) from the 5 loci, and tested 1062 SNPs for association with FEV1 from 2,729 subjects of the Korea Healthy Twin study. We identified TMEM132C as a potential candidate gene at 12q24.3, which is a previously reported locus of asthma and spirometric indices. We also found two adjacent candidate genes (UNC93A and TTLL2) in the 6q27 region, which has been previously identified as a pulmonary function locus in the Framingham cohort study. Our findings suggest that novel candidate genes (TMEM132C, UNC93A and TTLL2) in two different regions are associated with pulmonary function in a population in northeast Asia.
通过测量一秒用力呼气量(FEV1)进行肺功能的肺量计测量是一种可遗传的性状,反映了肺和气道的生理状况。全基因组连锁和关联研究已经确定了许多与肺功能相关的基因和遗传位点。然而,针对亚洲人群的研究报告数量有限。在本研究中,我们旨在调查东北亚人群中肺功能的遗传证据。我们对来自72个蒙古族家庭的706名GENDISCAN研究参与者进行了基于家系的关联测试,以确定肺功能的候选遗传决定因素。为了进行重复验证,我们从5个位点中选择了7个候选单核苷酸多态性(SNP),并对来自韩国健康双胞胎研究的2729名受试者的1062个SNP与FEV1的关联性进行了测试。我们确定跨膜蛋白132C(TMEM132C)是位于12q24.3的一个潜在候选基因,该位点是先前报道的哮喘和肺量计指标的位点。我们还在6q27区域发现了两个相邻的候选基因(UNC93A和微管酪氨酸连接酶样蛋白2,TTLL2),该区域在弗雷明汉队列研究中先前已被确定为肺功能位点。我们的研究结果表明,两个不同区域的新候选基因(TMEM132C、UNC93A和TTLL2)与东北亚人群的肺功能相关。