Literature DB >> 7581400

Allele-specific competitive blocker PCR: a one-step method with applicability to pool screening.

A Orou1, B Fechner, G Utermann, H J Menzel.   

Abstract

We have developed a novel one-step pool screening PCR procedure which is based on the principles of amplification refractory mutation system (ARMS) and competitive oligonuleotide priming (COP) PCR. In addition to the usual primers, this approach uses two allele-specific competitive oligonucleotides, one of which is 3'-end labeled with a dideoxynucleotide and blocks amplification of the wild-type allele. An allele-specific product is generated only in the presence of the mutation. The introduction of an allele-specific competitive blocker oligonucleotide improves the specificity and robustness of ARMS-PCR. Further its sensitivity is dramatically increased, which allows detection of one mutant allele in a large excess of wild-type-bearing genomic DNA by electrophoresis in an ethidium bromide-stained agarose gel (up to 1 in 10(4) alleles). This makes the method ideal for nonradioactive pool screening. The successful application of the method has been demonstrated for four different point mutations, two in the apolipoprotein B gene (R3500Q, R3531C) which result in familial defective apolipoprotein B-100, one in the CFTR gene (R1162X), and one in the gene for lipoprotein lipase (G188E).

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Year:  1995        PMID: 7581400     DOI: 10.1002/humu.1380060209

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  8 in total

1.  Detection of apoB-100 R3500Q mutation by competitive allele-specific polymerase chain reaction.

Authors:  A D Horvath; S A Kirov; E E Karaulanov; V S Ganev
Journal:  J Clin Lab Anal       Date:  2001       Impact factor: 2.352

2.  Headloop suppression PCR and its application to selective amplification of methylated DNA sequences.

Authors:  Keith N Rand; Thu Ho; Wenjia Qu; Susan M Mitchell; Rose White; Susan J Clark; Peter L Molloy
Journal:  Nucleic Acids Res       Date:  2005-08-09       Impact factor: 16.971

3.  Extendable blocking probe in reverse transcription for analysis of RNA variants with superior selectivity.

Authors:  Tho H Ho; Kien X Dang; Susanna Lintula; Kristina Hotakainen; Lin Feng; Vesa M Olkkonen; Emmy W Verschuren; Tuomas Tenkanen; Caj Haglund; Kaija-Leena Kolho; Ulf-Hakan Stenman; Jakob Stenman
Journal:  Nucleic Acids Res       Date:  2014-11-05       Impact factor: 16.971

4.  A simple and robust real-time qPCR method for the detection of PIK3CA mutations.

Authors:  Virginia Alvarez-Garcia; Clare Bartos; Ieva Keraite; Urmi Trivedi; Paul M Brennan; Maïwenn Kersaudy-Kerhoas; Karim Gharbi; Olga Oikonomidou; Nicholas R Leslie
Journal:  Sci Rep       Date:  2018-03-09       Impact factor: 4.379

5.  Mutation detection by real-time PCR: a simple, robust and highly selective method.

Authors:  John Morlan; Joffre Baker; Dominick Sinicropi
Journal:  PLoS One       Date:  2009-02-25       Impact factor: 3.240

6.  Quantitative threefold allele-specific PCR (QuanTAS-PCR) for highly sensitive JAK2 V617F mutant allele detection.

Authors:  Giada V Zapparoli; Robert N Jorissen; Chelsee A Hewitt; Michelle McBean; David A Westerman; Alexander Dobrovic
Journal:  BMC Cancer       Date:  2013-04-24       Impact factor: 4.430

7.  Association of NQO1 polymorphism with spontaneous breast cancer in two independent populations.

Authors:  H-J Menzel; J Sarmanova; P Soucek; R Berberich; K Grünewald; M Haun; H-G Kraft
Journal:  Br J Cancer       Date:  2004-05-17       Impact factor: 7.640

8.  Detection of the transforming AKT1 mutation E17K in non-small cell lung cancer by high resolution melting.

Authors:  Hongdo Do; Benjamin Solomon; Paul L Mitchell; Stephen B Fox; Alexander Dobrovic
Journal:  BMC Res Notes       Date:  2008-05-16
  8 in total

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