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使用新型植物核酸内切酶进行突变检测。

Mutation detection using a novel plant endonuclease.

作者信息

Oleykowski C A, Bronson Mullins C R, Godwin A K, Yeung A T

机构信息

Fox Chase Cancer Center, 7701 Burholme Avenue, Philadelphia, PA 19111, USA.

出版信息

Nucleic Acids Res. 1998 Oct 15;26(20):4597-602. doi: 10.1093/nar/26.20.4597.

DOI:10.1093/nar/26.20.4597
PMID:9753726
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC147896/
Abstract

We have discovered a useful new reagent for mutation detection, a novel nuclease CEL I from celery. It is specific for DNA distortions and mismatches from pH 6 to 9. Incision is on the 3'-side of the mismatch site in one of the two DNA strands in a heteroduplex. CEL I-like nucleases are found in many plants. We report here that a simple method of enzyme mutation detection using CEL I can efficiently identify mutations and polymorphisms. To illustrate the efficacy of this approach, the exons of the BRCA1 gene were amplified by PCR using primers 5'-labeled with fluorescent dyes of two colors. The PCR products were annealed to form heteroduplexes and subjected to CEL I incision. In GeneScan analyses with a PE Applied Biosystems automated DNA sequencer, two independent incision events, one in each strand, produce truncated fragments of two colors that complement each other to confirm the position of the mismatch. CEL I can detect 100% of the sequence variants present, including deletions, insertions and missense alterations. Our results indicate that CEL I mutation detection is a highly sensitive method for detecting both polymorphisms and disease-causing mutations in DNA fragments as long as 1120 bp in length.

摘要

我们发现了一种用于突变检测的有用新试剂,即一种来自芹菜的新型核酸酶CEL I。它对pH值6至9范围内的DNA扭曲和错配具有特异性。切割发生在异源双链体中两条DNA链之一的错配位点的3'侧。在许多植物中都发现了类似CEL I的核酸酶。我们在此报告,一种使用CEL I进行酶促突变检测的简单方法能够有效地识别突变和多态性。为了说明这种方法的有效性,使用两种颜色的荧光染料标记5'端的引物通过PCR扩增BRCA1基因的外显子。PCR产物退火形成异源双链体并进行CEL I切割。在使用PE Applied Biosystems自动DNA测序仪进行的基因扫描分析中,两个独立的切割事件,每条链各一个,产生两种颜色的截短片段,它们相互补充以确认错配的位置。CEL I能够检测出所有存在的序列变异,包括缺失、插入和错义改变。我们的结果表明,CEL I突变检测是一种高度灵敏的方法,可用于检测长度达1120 bp的DNA片段中的多态性和致病突变。