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高分辨率熔解曲线分析用于基因扫描。

High resolution melting analysis for gene scanning.

机构信息

ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT 84108, USA.

出版信息

Methods. 2010 Apr;50(4):250-61. doi: 10.1016/j.ymeth.2010.01.013. Epub 2010 Jan 18.

Abstract

High resolution melting is a new method of genotyping and variant scanning that can be seamlessly appended to PCR amplification. Limitations of genotyping by amplicon melting can be addressed by unlabeled probe or snapback primer analysis, all performed without labeled probes. High resolution melting can also be used to scan for rare sequence variants in large genes with multiple exons and is the focus of this article. With the simple addition of a heteroduplex-detecting dye before PCR, high resolution melting is performed without any additions, processing or separation steps. Heterozygous variants are identified by atypical melting curves of a different shape compared to wild-type homozygotes. Homozygous or hemizygous variants are detected by prior mixing with wild-type DNA. Design, optimization, and performance considerations for high resolution scanning assays are presented for rapid turnaround of gene scanning. Design concerns include primer selection and predicting melting profiles in silico. Optimization includes temperature gradient selection of the annealing temperature, random population screening for common variants, and batch preparation of primer plates with robotically deposited and dried primer pairs. Performance includes rapid DNA preparation, PCR, and scanning by high resolution melting that require, in total, only 3h when no variants are present. When variants are detected, they can be identified in an additional 3h by rapid cycle sequencing and capillary electrophoresis. For each step in the protocol, a general overview of principles is provided, followed by an in depth analysis of one example, scanning of CYBB, the gene that is mutated in X-linked chronic granulomatous disease.

摘要

高分辨率熔解曲线分析是一种新的基因分型和变异扫描方法,可无缝附加于 PCR 扩增。通过非标记探针或回切引物分析可以解决扩增片段熔解曲线基因分型的局限性,所有这些分析都无需标记探针。高分辨率熔解曲线分析还可用于扫描具有多个外显子的大基因中的稀有序列变异,这也是本文的重点。通过在 PCR 之前简单地添加异源双链检测染料,高分辨率熔解曲线分析无需添加任何试剂、进行任何处理或分离步骤。与野生型纯合子相比,杂合变体的非典型熔解曲线形状可识别出其不同之处。通过与野生型 DNA 预先混合,可以检测到纯合子或半合子变体。本文提出了用于快速基因扫描的高分辨率扫描分析的设计、优化和性能考虑因素。设计关注包括引物选择和计算机预测熔解曲线。优化包括退火温度的温度梯度选择、常见变异的随机群体筛选以及使用机器人沉积和干燥的引物对进行引物板的批量制备。性能包括快速的 DNA 制备、PCR 和高分辨率熔解曲线扫描,如果不存在变体,总共只需要 3 小时。如果检测到变体,则可以通过快速循环测序和毛细管电泳在另外 3 小时内识别出它们。对于该方案的每个步骤,首先提供原理的概述,然后对一个示例进行深入分析,即扫描突变导致 X 连锁慢性肉芽肿病的 CYBB 基因。

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