全血、干血点和尿液中人红细胞生成素基因第5外显子c.577del变体的检测

F. Donati, L. Concetti, X. de la Torre, Xinmiao Zhou, Lisi Zhang, F. Botré
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引用次数: 1

摘要

背景:在兴奋剂控制中,人类红细胞生成素基因外显子5 c.577del变体的存在可能是解释目前有效的基于SDS-PAGE和/或SAR-PAGE免疫电泳检测人类重组红细胞生成蛋白的分析方法结果的一个混淆因素。这种决定高分子量蛋白质转录的变体可能错误地表明生物样本中存在重组红细胞生成素,从而导致假阳性结果的可能性。尽管该变种现在只在东亚人群中被发现,而且频率非常低,但它可能威胁到目前反兴奋剂检测的可靠性。方法:我们进行了基因测试,以确定目前收集的用于反兴奋剂分析的生物样本(全血、尿液和干血点)中是否存在这种变体。该测试基于人类红细胞生成素基因外显子5的Sanger测序,c.577del变体位于该外显子。结果和讨论:该方法具有100%的特异性,并允许从每个生物样本中提取的100pg基因组DNA开始识别变体的可能存在。通过对显示和未显示外显子c.577del变体的受试者的真实样本进行分析,证实了该测试的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of exon 5 c.577del variant of human erythropoietin gene in whole blood, dried blood spots and urine samples for doping control
Background: In doping control, the presence of the exon5 c.577del variant in the human erythropoietin gene may be a confounding factor in the interpretation of the results from the analytical method currently in force for the detection of human recombinant erythropoietin, based on immunoelectrophoresis on SDS-PAGE and/or SAR-PAGE. This variant, determining the transcription of a higher molecular weight protein, can erroneously suggest the presence of recombinant erythropoietin in a biological sample, causing the possibility of a false positive result. Although the variant was now identified only in East Asian populations and with a very low frequency, it can threaten the reliability of current anti-doping tests.Methods: We have implemented a genetic test to identify the presence of this variant in the biological samples that are presently collected for anti-doping analysis (whole blood, urine, and dried blood spots). The test is based on the Sanger sequencing of the human erythropoietin gene exon 5, where the c.577del variant falls.Results and Discussion: The method has a specificity of 100% and allows identification of the possible presence of the variant starting from 100 pg of genomic DNA extracted from each biological sample. The efficacy of the test has been confirmed by the analysis of real samples from subjects showing and not showing the exon c.577del variant.
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