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条件性置换杂交分析多重 SNP 相位。

Conditional Displacement Hybridization Assay for Multiple SNP Phasing.

机构信息

Department of Chemical and Biomolecular Engineering and ‡Division of Biomedical Engineering, The Hong Kong University of Science and Technology , Clear Water Bay, Kowloon, Hong Kong.

出版信息

Anal Chem. 2017 Sep 19;89(18):9961-9966. doi: 10.1021/acs.analchem.7b02300. Epub 2017 Aug 25.

Abstract

The two chromosomal copies of the human genome are highly polymorphic, and the allelic content on each strand can dictate a person's biological outcomes. While many of the current diagnostic tools are able to detect the presence of multiple mutations at the same time, most cannot determine the phase of these mutations unless long-range PCR or sequencing techniques are used or if templates are compartmentalized into single copies prior to amplification. Here, an enzyme-coupled hybridization assay, named conditional displacement hybridization assay (CDHA), is described for the concurrent and rapid determination of the presence and phase of SNP variants. In this approach, short DNA probes were utilized to first quantify the amount of SNPs on the templates using a two-channel fluorescence measurement. The hybrids formed between the probes and the templates then set up the right condition for the subsequent enzymatic displacement and quenching of a fluorophore-labeled strand, which happens only if both SNPs are present on the same strand. The drop in the fluorescence signal thereby indicates the phase of the two SNPs. As a proof of concept, we tested the assay on four variants of an arbitrary sequence-with or without mutation on two sites 100 nts apart. The assay described herein was able to determine the haplotype phase of the samples in less than 1 h. This method promises a direct, cost-effective, and laboratory-based test to extract further genetic information to determine and/or predict diseases and traits dependent on SNP phasing.

摘要

人类基因组的两条染色体拷贝高度多态性,每条链上的等位基因含量可以决定一个人的生物学结果。虽然许多当前的诊断工具能够同时检测到多种突变的存在,但大多数情况下,如果不使用长距离 PCR 或测序技术,或者在扩增前将模板分区成单拷贝,则无法确定这些突变的相位。在这里,描述了一种酶偶联杂交测定法,称为条件置换杂交测定法(CDHA),用于同时快速确定 SNP 变体的存在和相位。在这种方法中,短 DNA 探针首先用于使用双通道荧光测量来定量模板上 SNP 的数量。探针与模板形成的杂交体随后为随后的酶置换和荧光标记链的淬灭建立了正确的条件,只有当两条 SNP 都位于同一条链上时才会发生这种情况。荧光信号的下降表明两条 SNP 的相位。作为概念验证,我们在相隔 100 个核苷酸的两个位点上有无突变的任意序列的四个变体上测试了该测定法。本文所述的测定法能够在不到 1 小时的时间内确定样本的单倍型相位。该方法有望成为一种直接、经济有效的基于实验室的测试方法,以提取更多的遗传信息,用于确定和/或预测依赖于 SNP 相位的疾病和特征。

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