Sahota Jatinder Singh, Guleria Kamlesh, Sambyal Vasudha
Cytogenetics Laboratory, Department of Human Genetics, Guru Nanak Dev University (GNDU), Amritsar, Punjab, 143005, India.
Biochem Genet. 2025 Feb;63(1):730-760. doi: 10.1007/s10528-024-10743-3. Epub 2024 Mar 21.
XRCC1 is involved in repair of single-strand breaks generated by mutagenic exposure. Polymorphisms within XRCC1 affect its ability to efficiently repair DNA damage. Polycyclic aromatic hydrocarbons or PAHs are genotoxic compounds which form bulky DNA adducts that are linked with infertility. Few reports suggest combined role of XRCC1 polymorphisms and PAHs in infertility. Present study investigates association of three XRCC1 polymorphisms (p.Arg194Trp, p.Arg280His, p.Arg399Gln) with male and female infertility in a North-West Indian population using case-control approach. Additionally, in silico approach has been used to predict whether XRCC1 polymorphisms effect interaction of XRCC1 with different PAHs. For case-control study, XRCC1 polymorphisms were screened in peripheral blood samples of age- and gender-matched 201 infertile cases (♂-100, ♀-101) and 201 fertile controls (♂-100, ♀-101) using PCR-RFLP method. For in silico study, AutoDock v4.2.6 was used for molecular docking of B[a]P, BPDE-I, ( ±)-anti-BPDE, DB[a,l]P, 1-N, 2-N, 1-OHP, 2-OHF with XRCC1 and assess effect of XRCC1 polymorphisms on their interaction. In case-control study, statistical analysis showed association of XRCC1 p.Arg280His GA genotype (p = 0.027), A allele (p = 0.019) with reduced risk of male infertility. XRCC1 p.Arg399Gln AA genotype (p = 0.021), A allele (p = 0.014) were associated with reduced risk for female primary infertility. XRCC1 p.Arg194Trp T allele was associated with increased risk for female infertility (p = 0.035). In silico analysis showed XRCC1-PAH interaction with non-significant effect of XRCC1 polymorphisms on predicted binding. Therefore, present study concludes that XRCC1 polymorphism-modified risk for male and female infertility in North-West Indians without significant effect on predicted XRCC1-PAH interactions. This is the first report on XRCC1 in female infertility.
XRCC1参与由诱变暴露产生的单链断裂的修复。XRCC1内的多态性影响其有效修复DNA损伤的能力。多环芳烃(PAHs)是具有遗传毒性的化合物,可形成与不孕症相关的大分子DNA加合物。很少有报告表明XRCC1多态性和PAHs在不孕症中的联合作用。本研究采用病例对照方法,调查了印度西北部人群中三种XRCC1多态性(p.Arg194Trp、p.Arg280His、p.Arg399Gln)与男性和女性不孕症的关联。此外,还采用了计算机模拟方法来预测XRCC1多态性是否会影响XRCC1与不同PAHs的相互作用。在病例对照研究中,使用PCR-RFLP方法对年龄和性别匹配的201例不孕病例(男性100例,女性101例)和201例生育对照(男性100例,女性101例)的外周血样本进行XRCC1多态性筛查。在计算机模拟研究中,使用AutoDock v4.2.6对苯并[a]芘、BPDE-I、(±)-反式-BPDE、二苯并[a,l]芘、1-N、2-N、1-OHP、2-OHF与XRCC1进行分子对接,并评估XRCC1多态性对它们相互作用的影响。在病例对照研究中,统计分析表明,XRCC1 p.Arg280His GA基因型(p = 0.027)、A等位基因(p = 0.019)与男性不育风险降低相关。XRCC1 p.Arg399Gln AA基因型(p = 0.021)、A等位基因(p = 0.014)与女性原发性不孕风险降低相关。XRCC1 p.Arg194Trp T等位基因与女性不孕风险增加相关(p = 0.035)。计算机模拟分析表明XRCC1与PAHs存在相互作用,但XRCC1多态性对预测结合无显著影响。因此,本研究得出结论,XRCC1多态性改变了印度西北部男性和女性的不孕风险,对预测的XRCC1与PAHs的相互作用无显著影响。这是关于XRCC1在女性不孕症中的首次报道。