Simultaneous Genotyping of Multiple Somatic Mutations by Using a Clamping PNA and PNA Detection Probes

被引:20
|
作者
Kim, Yong-Tae [2 ]
Kim, Jin Woo [2 ]
Kim, Sung Kee [2 ]
Joe, Goon Ho [2 ]
Hong, In Seok [1 ]
机构
[1] Kongju Natl Univ, Coll Nat Sci, Dept Chem, Gongju Si 314701, Chungnam, South Korea
[2] Panagene Inc, Res Inst, Taejon 305510, South Korea
基金
新加坡国家研究基金会;
关键词
cancer; gamma-PNA; multiple genotyping; peptide nucleic acid; quantitative PCR; somatic mutations; PEPTIDE NUCLEIC-ACID; CELL LUNG-CANCER; REAL-TIME PCR; SENSITIVE DETECTION; KRAS MUTATIONS; HYBRIDIZATION; SAMPLES; LYSINE; DNA;
D O I
10.1002/cbic.201402640
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has been very difficult to detect and quantify multiple somatic mutations simultaneously in single-tube qPCR. Here, a novel method for simultaneous detection of multiple mutations and a melting curve analysis was developed by using clamping PNA and detection PNA probes. Each PNA probe was designed to have a specific melting temperature by the introduction of gamma-PNA monomer. This technique was successfully applied to the detection of six genotypes in two different mutations of K-RAS at the same time. Such simultaneous analysis of an amplified curve and a melting curve in qPCR can be widely used for the early diagnosis of cancer and determining the prognosis of drug treatments.
引用
收藏
页码:209 / 213
页数:5
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