Achmüller Clemens, Köhler Andrea, Bösch Sylvia, Schneider Rainer
Institute of Biochemistry and Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Innsbruck, Austria.
Biotechniques. 2008 Nov;45(5):577-80. doi: 10.2144/000112948.
In this study we present a quick and easy method for counting trinucleotide repeats by de-oxyadenosine overhang (A-overhang)-dependent repeat expansion determination (ADRED). During standard Taq DNA polymerase-based sequencing reactions, the unterminated sequencing products of short PCR fragments are tagged with a 3'-end A-overhang that is visible as an intense peak in an electropherogram; this allows for easy and precise determination of the fragment length and thus the extent of repeat expansions. ADRED has clear advantages over existing methods, because repeat numbers of both normal and pathogenic (expanded) alleles can be analyzed without using labeled primers or labeled DNA standards. Because ADRED includes a sequencing step, disease-relevant polymorphisms (e.g., CAA interruptions in spinocerebellar ataxia type 2) can simultaneously be detected.
在本研究中,我们提出了一种通过基于脱氧腺苷突出端(A突出端)的重复序列扩增测定(ADRED)来快速简便地计数三核苷酸重复序列的方法。在基于Taq DNA聚合酶的标准测序反应过程中,短PCR片段的未终止测序产物会被3'端A突出端标记,该突出端在电泳图中表现为一个强烈的峰;这使得能够轻松精确地确定片段长度,进而确定重复序列扩增的程度。与现有方法相比,ADRED具有明显优势,因为无需使用标记引物或标记DNA标准品即可分析正常和致病(扩增)等位基因的重复次数。由于ADRED包括一个测序步骤,因此可以同时检测与疾病相关的多态性(例如,2型脊髓小脑共济失调中的CAA中断)。