Polymorphisms and expression levels of TNP2, SYCP3, and AZFa genes in patients with azoospermia.

Journal Des Maladies Vasculaires Pub Date : 2023-12-01 Epub Date: 2023-09-06 DOI:10.5653/cerm.2023.06219
Mohammad Ismael Ibrahim Jebur, Narges Dastmalchi, Parisa Banamolaei, Reza Safaralizadeh
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Abstract

Objective: Azoospermia (the total absence of sperm in the ejaculate) affects approximately 10% of infertile males. Despite diagnostic advances, azoospermia remains the most challenging issue associated with infertility treatment. Our study evaluated transition nuclear protein 2 (TNP2) and synaptonemal complex protein 3 (SYCP3) polymorphisms, azoospermia factor a (AZFa) microdeletion, and gene expression levels in 100 patients with azoospermia.

Methods: We investigated a TNP2 single-nucleotide polymorphism through polymerase chain reaction (PCR) restriction fragment length polymorphism analysis using a particular endonuclease. An allele-specific PCR assay for SYCP3 was performed utilizing two forward primers and a common reverse primer in two PCR reactions. Based on the European Academy of Andrology guidelines, AZFa microdeletions were evaluated by multiplex PCR. TNP2, SYCP3, and the AZFa region main gene (DEAD-box helicase 3 and Y-linked [DDX3Y]) expression levels were assessed via quantitative PCR, and receiver operating characteristic curve analysis was used to determine the diagnostic capability of these genes.

Results: The TNP2 genotyping and allelic frequency in infertile males did not differ significantly from fertile volunteers. In participants with azoospermia, the allelic frequency of the SYCP3 mutant allele (C allele) was significantly altered. Deletion of sY84 and sY86 was discovered in patients with azoospermia and oligozoospermia. Moreover, SYCP3 and DDX3Y showed decreased expression levels in the azoospermia group, and they exhibited potential as biomarkers for diagnosing azoospermia (area under the curve, 0.722 and 0.720, respectively).

Conclusion: These results suggest that reduced SYCP3 and DDX3Y mRNA expression profiles in testicular tissue are associated with a higher likelihood of retrieving spermatozoa in individuals with azoospermia. The homozygous genotype TT of the SYCP3 polymorphism was significantly associated with azoospermia.

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无精子症患者TNP2、SYCP3和AZFa基因多态性及其表达水平
目的:无精子症(射精中完全没有精子)影响大约10%的不育男性。尽管诊断有了进步,无精子症仍然是不孕治疗中最具挑战性的问题。本研究评估了100例无精子症患者的过渡核蛋白2 (TNP2)和突触复合体蛋白3 (SYCP3)多态性、无精子症因子a (AZFa)微缺失和基因表达水平。方法:利用特定的内切酶,通过聚合酶链反应(PCR)限制性片段长度多态性分析,研究了TNP2单核苷酸多态性。在两个PCR反应中,利用两个正向引物和一个共同的反向引物进行SYCP3等位基因特异性PCR检测。根据欧洲男科学会指南,用多重PCR评估AZFa微缺失。通过定量PCR检测TNP2、SYCP3和AZFa区主基因(DEAD-box解旋酶3和Y-linked [DDX3Y])的表达水平,并通过受试者工作特征曲线分析确定这些基因的诊断能力。结果:不育男性的TNP2基因分型和等位基因频率与可育志愿者无显著差异。在无精子症患者中,SYCP3突变等位基因(C等位基因)的等位基因频率显著改变。在无精子症和少精子症患者中发现了sY84和sY86的缺失。此外,SYCP3和DDX3Y在无精子症组中表达水平下降,它们具有作为诊断无精子症的生物标志物的潜力(曲线下面积分别为0.722和0.720)。结论:这些结果表明,睾丸组织中SYCP3和DDX3Y mRNA表达谱的降低与无精子症患者取回精子的可能性增加有关。SYCP3多态性的纯合子基因型TT与无精子症显著相关。
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来源期刊
Journal Des Maladies Vasculaires
Journal Des Maladies Vasculaires 医学-外周血管病
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