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基于毛细管电泳的单链DNA构象分析用于高通量突变筛查。

Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening.

作者信息

Andersen Paal Skytt, Jespersgaard Cathrine, Vuust Jens, Christiansen Michael, Larsen Lars Allan

机构信息

Department of Clinical Biochemistry, Statens Serum Institute, Copenhagen, Denmark.

出版信息

Hum Mutat. 2003 May;21(5):455-65. doi: 10.1002/humu.10169.

Abstract

The generation of the draft human genome sequence has created new possibilities for diagnosis, prevention, and treatment of human disease. One consequence of these new possibilities is an increasing need for methods and technology that can be used for high-throughput screening for mutations in large DNA sample materials. In recent years, a number of mutation screening methods have emerged that are based on the analysis of sequence-dependent changes in the conformation of single- and double-stranded DNA using capillary electrophoresis. Common features of these methods are high sensitivity and reproducibility as well as the possibility for automation and massive parallelization. Thus, at present they are among the most attractive technologies for high-throughput mutation screening. This review describes the recent advances in capillary electrophoresis-based single strand conformation polymorphism (CE-SSCP) for detection of unknown mutations, and assesses its practical usability for high-throughput mutation screening based on the available literature. In addition, future prospects are outlined in light of the recent advances in microchip-based capillary electrophoresis.

摘要

人类基因组序列草图的绘制为人类疾病的诊断、预防和治疗创造了新的可能性。这些新可能性带来的一个后果是,对可用于对大量DNA样本材料进行高通量突变筛查的方法和技术的需求日益增加。近年来,出现了一些基于使用毛细管电泳分析单链和双链DNA构象中序列依赖性变化的突变筛查方法。这些方法的共同特点是灵敏度高、可重复性好,以及具有自动化和大规模并行化的可能性。因此,目前它们是高通量突变筛查中最具吸引力的技术之一。本综述描述了基于毛细管电泳的单链构象多态性(CE-SSCP)在检测未知突变方面的最新进展,并根据现有文献评估其在高通量突变筛查中的实际可用性。此外,鉴于基于微芯片的毛细管电泳的最新进展,还概述了未来的前景。

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