母体血浆中游离胎儿 DNA 的基因分析。

H Chen, T Wang, G He, L Zhu, T Ma
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引用次数: 0

摘要

为了研究将母体血浆中的游离胎儿 DNA 作为无创产前诊断中胎儿材料来源的可行性,我们采用引物延伸预扩增(PEP)和探针微板杂交技术对 65 份样本的母血中游离 DNA 的 SRY 基因进行了分析。结果表明,单独使用探针微孔板杂交和探针微孔板杂交加 PEP 检测怀有男胎的妇女母血中 SRY 基因的检出率分别为 76.09%(35/46)和 95.65%(44/46),两者之间存在显著差异。怀有女胎的妇女血液样本中 SRY 基因的未检出率为 100%(19/19)。这表明探针微孔板杂交是检测母体血浆中痕量胎儿DNA的有效方法,而两种技术的联合使用可大大提高灵敏度。分析母体血浆中的胎儿 DNA 可作为无创产前诊断的替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene analysis of free fetal DNA in maternal plasma.

To investigate the feasibility of using free fetal DNA from maternal plasma as the source of fetal material in non-invasive prenatal diagnosis, SRY gene of free DNA in maternal blood of 65 samples were analyzed by using primer extension preamplication (PEP) and probe microplate hybridization techniques. The results showed that the detection rate of SRY gene in maternal blood from women carrying male fetuses detected by probe microplate hybridization alone and probe microplate hybridization with PEP were 76.09% (35/46) and 95.65% (44/46) respectively, and there was a significant difference between them. The non-detection rate of SRY gene in blood samples from women carrying female fetus was 100% (19/19). It is indicated that probe microplate hybridization was an effective method in detecting trace fetal DNA from maternal plasma and the sensitivity could be substantially improved by combined use of the two techniques. Analysis of fetal DNA in maternal plasma can serve as an alternative for non-invasive prenatal diagnosis.

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