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无精子症患者中TNP2、SYCP3和AZFa基因的多态性及表达水平

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

作者信息

Jebur Mohammad Ismael Ibrahim, Dastmalchi Narges, Banamolaei Parisa, Safaralizadeh Reza

机构信息

Department of Animal Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.

Department of Biology, University College of Nabi Akram, Tabriz, Iran.

出版信息

Clin Exp Reprod Med. 2023 Dec;50(4):253-261. doi: 10.5653/cerm.2023.06219. Epub 2023 Sep 6.

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.

摘要

目的

无精子症(精液中完全没有精子)影响约10%的不育男性。尽管诊断技术有所进步,但无精子症仍然是不育治疗中最具挑战性的问题。我们的研究评估了100例无精子症患者的过渡性核蛋白2(TNP2)和联会复合体蛋白3(SYCP3)多态性、无精子症因子a(AZFa)微缺失以及基因表达水平。

方法

我们通过聚合酶链反应(PCR)限制性片段长度多态性分析,使用特定的内切酶研究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对SYCP3进行等位基因特异性PCR检测。根据欧洲男科学会指南,通过多重PCR评估AZFa微缺失。通过定量PCR评估TNP2、SYCP3和AZFa区域主要基因(DEAD盒解旋酶3和Y连锁[DDX3Y])的表达水平,并使用受试者工作特征曲线分析来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生育志愿者相比无显著差异。在无精子症患者中,SYCP3突变等位基因(C等位基因)的等位基因频率发生了显著改变。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在无精子症组中的表达水平降低,它们具有作为无精子症诊断生物标志物的潜力(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表达谱降低与无精子症个体获取精子的可能性较高有关。SYCP3多态性的纯合基因型TT与无精子症显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a271/10711250/136b0be94739/cerm-2023-06219f1.jpg

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