Department of Biotechnology and Bioinformatics, Jaypee University of Information Technology, Solan, Himachal Pradesh, India.
Department of Molecular Biology and Biochemistry, Guru Nanak Dev University, Amritsar, Punjab, India.
J Asthma. 2024 May;61(5):472-478. doi: 10.1080/02770903.2023.2289156. Epub 2023 Dec 6.
Genetic background and environmental stimuli play an important role in asthma, which is an individual's hyper-responsiveness to these stimuli leading to airway inflammation. Autophagy Related Gene 5 (ATG5) plays a critical role in the autophagy pathway and has been shown to be involved in asthma. The genetic polymorphisms in the ATG5 have been reported to predispose individuals to asthma. The role of single nucleotide polymorphism rs17587319 (C/G) of ATG5 in asthma has not been studied so far. Materials and methods: In this study, we in silico analysed rs17587319 (C/G) using web-based tools Human Splice Finder (HSF) and RegulomeDB and further a case-control study was conducted that included 187 blood samples (94 asthmatic and 93 healthy controls). In silico analysis suggested alteration of splicing signals by this intronic variant. The samples were genotyped by applying the PCR-RFLP method. The MAF obtained was 0.022 and 0.043 in healthy controls and asthmatic individuals, respectively. The statistical analysis revealed no association (allelic model, OR = 2.02, 95%CI = 0.59-6.83, = 0.25; co-dominant model, OR = 2.06, 95%CI = 0.6-7.12, = 0.24) of rs17587319 (C/G) with the susceptibility to asthma in the north Indian population. In conclusion, rs17587319 (C/G) of ATG5 does not predispose individuals to asthma in our part of the world. Further studies are needed including more number of samples to ascertain the role of this polymorphism in asthma.
遗传背景和环境刺激在哮喘中起着重要作用,这是个体对这些刺激的过度反应导致气道炎症。自噬相关基因 5(ATG5)在自噬途径中起着关键作用,并且已经显示与哮喘有关。ATG5 的遗传多态性已被报道易患哮喘。ATG5 单核苷酸多态性 rs17587319(C/G)在哮喘中的作用尚未得到研究。
在这项研究中,我们使用基于网络的工具 Human Splice Finder(HSF)和 RegulomeDB 对 rs17587319(C/G)进行了计算机分析,进一步进行了病例对照研究,该研究包括 187 个血液样本(94 例哮喘和 93 例健康对照)。计算机分析表明,这种内含子变异改变了剪接信号。通过应用 PCR-RFLP 方法对样本进行了基因分型。MAF 在健康对照组和哮喘组中分别为 0.022 和 0.043。统计分析显示,rs17587319(C/G)与北印度人群哮喘易感性之间没有关联(等位基因模型,OR=2.02,95%CI=0.59-6.83,=0.25;共显性模型,OR=2.06,95%CI=0.6-7.12,=0.24)。
在我们所在的地区,ATG5 的 rs17587319(C/G)不会使个体易患哮喘。需要进一步研究包括更多样本,以确定该多态性在哮喘中的作用。