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Possible Association of FAS and FASLG Polymorphisms with the Risk of Idiopathic Azoospermia in Southeast Turkey

机译:FAS和FASLG多态性与土耳其东南部特发性无精症风险的可能关联

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摘要

To investigate the association of the genetic variants of FASIFASLG cell death pathway genes in male infertility, we genotyped the FAS -670A/G, - 1377G/A, and FASLG - 124A/G single-nucleotide polymorphisms (SNPs) by real-time polymerase chain reaction in 108 infertile men with idiopathic azoospermia and in 125 proven fertile controls. The distribution of genotypes and alleles for SNPs at FAS - 1377G/A and FASLG - 124A/G loci were determined not to be statistically different between the case and control groups. However, the genotype frequencies of SNPs, FAS - 670AA and FAS - 670AG, were found to be significantly different between the case and control groups. Whereas the FAS -670AA genotype might be regarded as a higher predisposition for idiopathic azoospermia, FAS - 670AG could be interpreted to mean that this genotype provides protection against idiopathic azoospermia. The study of combined genotype and haplotype frequencies has found statistically significant differences between case and control subjects for some combinations. The AA-GG binary genotype for the FAS670 and FAS1377 loci couple, in particular, may have a high degree of predisposition to idiopathic azoospermia. Our results suggest that FAS - 670A/G SNP may be a genetic predisposing factor of idiopathic azoospermia among southeastern Anatolian men. Larger studies are needed to verify these findings. Furthermore, our data indicated a possible linkage between the FAS and FASLG genes and idiopathic azoospermia.
机译:为了研究FASIFASLG细胞死亡途径基因在男性不育症中的遗传变异的关联,我们通过实时聚合酶对FAS -670A / G,-1377G / A和FASLG-124A / G单核苷酸多态性(SNP)进行了基因分型108名患有特发性无精症的不育男性和125位经证实的受精对照中的链反应。确定病例组和对照组之间在FAS-1377G / A和FASLG-124A / G位点的SNP的基因型和等位基因的分布没有统计学差异。然而,在病例组和对照组之间发现SNPs的基因型频率FAS-670AA和FAS-670AG显着不同。 FAS -670AA基因型可能被认为是特发性无精子症的较高易感性,而FAS-670AG基因型可以被解释为意味着该基因型提供了针对特发性无精子症的保护。对基因型和单倍型频率结合的研究发现,病例和对照受试者在某些组合上存在统计学上的显着差异。特别是,FAS670和FAS1377基因座对的AA-GG二元基因型可能对特发性无精症具有较高的易感性。我们的结果表明,FAS-670A / G SNP可能是东南部安那托利亚男性中特发性无精症的遗传诱因。需要更大的研究来验证这些发现。此外,我们的数据表明,FAS和FASLG基因与特发性无精症之间可能存在联系。

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  • 来源
    《Genetic testing and molecular biomarkers》 |2014年第6期|383-388|共6页
  • 作者单位

    Department of Medical Biology and Genetics Faculty of Medicine Dicle University Diyarbakir 21280 Turkey;

    Departments of Urology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey;

    Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey;

    Department of Medical Biology, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey;

    Department of Biostatistics, Faculty of Medicine, Dicle University, Diyarbakir, Turkey;

    Department of Medical Biology, Faculty of Medicine, Kahramanmaras Suetcue Imam University, Kahramanmaras, Turkey;

    Departments of Urology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey;

    Departments of Urology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey;

    Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey;

    Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
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  • 正文语种 eng
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