Larsen Lars Allan, Jespersgaard Cathrine, Andersen Paal Skytt
Wilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, University of Copenhagen, Blegdamsvej 3, DK-2200, Copenhagen, Denmark.
Nat Protoc. 2007;2(6):1458-66. doi: 10.1038/nprot.2007.200.
This protocol describes capillary array electrophoresis single-strand conformation polymorphism (CAE-SSCP), a screening method for detection of unknown and previously identified mutations. The method detects 98% of mutations in a sample material and can be applied to any organism where the goal is to determine genetic variation. This protocol describes how to screen for mutations in 192 singleplex or up to 768 multiplex samples over 3 days. The protocol is based on the principle of sequence-specific mobility of single-stranded DNA in a native polymer, and covers all stages in the procedure, from initial DNA purification to final CAE-SSCP data analysis, as follows: DNA is purified, followed by PCR amplification using fluorescent primers. After PCR amplification, double-stranded DNA is heat-denatured to separate the strands and subsequently cooled on ice to avoid reannealing. Finally, samples are analyzed by capillary electrophoresis and appropriate analysis software.
本方案描述了毛细管阵列电泳单链构象多态性分析(CAE - SSCP),这是一种用于检测未知突变和先前已鉴定突变的筛查方法。该方法可检测出样本材料中98%的突变,并且可应用于任何旨在确定遗传变异的生物体。本方案描述了如何在3天内对192个单样本或多达768个多样本进行突变筛查。该方案基于单链DNA在天然聚合物中序列特异性迁移的原理,涵盖了从初始DNA纯化到最终CAE - SSCP数据分析的整个过程,具体如下:先纯化DNA,然后使用荧光引物进行PCR扩增。PCR扩增后,双链DNA经热变性使链分离,随后在冰上冷却以避免重新退火。最后,通过毛细管电泳和适当的分析软件对样本进行分析。