Department of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Tsukuba Medical Center, Ibaraki, Japan.
Sci Rep. 2021 Sep 22;11(1):18791. doi: 10.1038/s41598-021-98348-3.
ETS variant transcription factor 4 (ETV4) is a recently identified transcription factor that regulates gene expression-based biomarkers of asthma and IL6 production in an airway epithelial cell line. Given that ETV4 has not yet been implicated in asthma genetics, we performed genetic association studies of adult asthma in the ETV4 region using two independent Japanese cohorts (a total of 1532 controls and 783 cases). SNPs located between ETV4 and mesenchyme homeobox 1 (MEOX1) were significantly associated with adult asthma, including rs4792901 and rs2880540 (P = 5.63E-5 and 2.77E-5, respectively). The CC haplotype of these two SNPs was also significantly associated with adult asthma (P = 8.43E-7). Even when both SNPs were included in a logistic regression model, the association of either rs4792901 or rs2880540 remained significant (P = 0.013 or 0.007, respectively), suggesting that the two SNPs may have independent effects on the development of asthma. Both SNPs were expression quantitative trait loci, and the asthma risk alleles at both SNPs were correlated with increased levels of ETV4 mRNA expression. In addition, the asthma risk allele at rs4792901 was associated with increased serum IL6 levels (P = 0.041) in 651 healthy adults. Our findings imply that ETV4 is involved in the pathogenesis of asthma, possibly through the heightened production of IL6.
ETS 变异转录因子 4(ETV4)是一种新发现的转录因子,它可调节气道上皮细胞系中哮喘和白细胞介素 6(IL6)产生的基于基因表达的生物标志物。鉴于 ETV4 尚未涉及哮喘遗传学,我们使用两个独立的日本队列(共 1532 名对照和 783 例病例)对 ETV4 区域的成人哮喘进行了遗传关联研究。位于 ETV4 和间充质同源盒 1(MEOX1)之间的 SNPs 与成人哮喘显著相关,包括 rs4792901 和 rs2880540(P=5.63E-5 和 2.77E-5)。这两个 SNPs 的 CC 单倍型也与成人哮喘显著相关(P=8.43E-7)。即使将这两个 SNP 都纳入逻辑回归模型,rs4792901 或 rs2880540 的关联仍然显著(P=0.013 或 0.007),表明这两个 SNP 可能对哮喘的发展有独立的影响。这两个 SNP 都是表达数量性状基因座,这两个 SNP 的哮喘风险等位基因与 ETV4 mRNA 表达水平的升高相关。此外,rs4792901 的哮喘风险等位基因与 651 名健康成年人的血清 IL6 水平升高相关(P=0.041)。我们的研究结果表明,ETV4 参与了哮喘的发病机制,可能是通过增加 IL6 的产生。