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临床检验医学中的高分辨率熔解应用

High resolution melting applications for clinical laboratory medicine.

作者信息

Erali Maria, Voelkerding Karl V, Wittwer Carl T

机构信息

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

出版信息

Exp Mol Pathol. 2008 Aug;85(1):50-8. doi: 10.1016/j.yexmp.2008.03.012. Epub 2008 Apr 13.

Abstract

Separation of the two strands of DNA with heat (melting) is a fundamental property of DNA that is conveniently monitored with fluorescence. Conventional melting is performed after PCR on any real-time instrument to monitor product purity (dsDNA dyes) and sequence (hybridization probes). Recent advances include high resolution instruments and saturating DNA dyes that distinguish many different species. For example, mutation scanning (identifying heterozygotes) by melting is closed-tube and has similar or superior sensitivity and specificity compared to methods that require physical separation. With high resolution melting, SNPs can be genotyped without probes and more complex regions can be typed with unlabeled hybridization probes. Highly polymorphic HLA loci can be melted to establish sequence identity for transplantation matching. Simultaneous genotyping with one or more unlabeled probes and mutation scanning of the entire amplicon can be performed at the same time in the same tube, vastly decreasing or eliminating the need for re-sequencing in genetic analysis. High resolution PCR product melting is homogeneous, closed-tube, rapid (1-5 min), non-destructive and does not require covalently-labeled fluorescent probes. In the clinical laboratory, it is an ideal format for in-house testing, with minimal cost and time requirements for new assay development.

摘要

通过加热使DNA的两条链分离(解链)是DNA的一项基本特性,利用荧光可方便地对其进行监测。常规解链是在PCR之后在任何实时仪器上进行,以监测产物纯度(双链DNA染料)和序列(杂交探针)。最近的进展包括高分辨率仪器和能区分许多不同物种的饱和DNA染料。例如,通过解链进行突变扫描(鉴定杂合子)是闭管操作,与需要物理分离的方法相比,具有相似或更高的灵敏度和特异性。通过高分辨率解链,可以在不使用探针的情况下对单核苷酸多态性(SNP)进行基因分型,并且可以使用未标记的杂交探针来分析更复杂的区域。高度多态的人类白细胞抗原(HLA)基因座可以通过解链来确定序列一致性,以进行移植配型。可以在同一管中同时使用一个或多个未标记的探针进行基因分型,并对整个扩增子进行突变扫描,这在很大程度上减少或消除了基因分析中重新测序的需求。高分辨率PCR产物解链是均相的、闭管的、快速的(1 - 5分钟)、非破坏性的,并且不需要共价标记的荧光探针。在临床实验室中,它是内部检测的理想形式,新检测方法开发的成本和时间要求最低。

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