Mollaahmadi Fahimeh, Moini Ashraf, Salman Yazdi Reza, Behmanesh Mehrdad
Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Department of Endocrinology and Female Infertility, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Cell J. 2018 Apr;20(1):73-77. doi: 10.22074/cellj.2018.4255. Epub 2017 Dec 1.
Infertility is a common human disorder which is defined as the failure to conceive for a period of 12 months without contraception. Many studies have shown that the outcome of fertility could be affected by DNA damage. We attempted to examine the association of two SNPs (rs1127354 and rs7270101) in ITPA, a gene encoding a key factor in the repair system, with susceptibility to infertility.
This was a case-control study of individuals with established infertility. Blood samples were obtained from 164 infertile patients and 180 ethnically matched fertile controls. Total genomic DNA were extracted from whole blood using the standard salting out method, and stored at -20˚C. Genotyping were based on mismatch polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method in which PCR products were digested with the XmnI restriction enzyme and run on a 12% polyacrylamide gel.
All genotype frequencies in the control group were in Hardy-Weinberg equilibrium. A significant association (in allelic, recessive and dominant genotypic models) was observed between infertile patients and healthy controls based on rs1127354 (P=0.0001), however, no significant association was detected for rs7270101. Also, gender stratification and analysis of different genotype models did not lead to a significant association for this singlenucleotide polymorphis (SNP).
ITPA is likely to be a genetic determinant for decreased fertility. To the best of our knowledge, this is the first report demonstrating this association, however, given the small sample size and other limitations, genotyping of this SNP is recommended to be carried out in different populations with more samples.
不孕症是一种常见的人类疾病,定义为在无避孕措施的情况下12个月内未能受孕。许多研究表明,生育结果可能会受到DNA损伤的影响。我们试图研究参与修复系统的关键因子编码基因ITPA中的两个单核苷酸多态性(SNP,rs1127354和rs7270101)与不孕症易感性之间的关联。
这是一项针对已确诊不孕症患者的病例对照研究。从164名不孕患者和180名种族匹配的可育对照者中采集血样。使用标准盐析法从全血中提取总基因组DNA,并储存在-20˚C。基因分型基于错配聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,其中PCR产物用XmnI限制性内切酶消化,并在12%聚丙烯酰胺凝胶上进行电泳。
对照组中所有基因型频率均处于哈迪-温伯格平衡。基于rs1127354,在不孕患者和健康对照者之间观察到显著关联(在等位基因、隐性和显性基因型模型中,P = 0.0001),然而,未检测到rs7270101有显著关联。此外,性别分层和不同基因型模型分析并未导致该单核苷酸多态性(SNP)出现显著关联。
ITPA可能是生育力下降的一个遗传决定因素。据我们所知,这是首次证明这种关联的报告,然而,鉴于样本量小和其他局限性,建议在更多样本的不同人群中对该SNP进行基因分型。