A new approach for point mutation detection based on a ligase chain reaction

被引:10
作者
Demchinskaya, AV
Shilov, IA
Karyagina, AS
Lunin, VG
Sergienko, OV
Voronina, OL
Leiser, M
机构
[1] Inst Agr Biotechnol, Moscow 127550, Russia
[2] MIRA Diagnost, D-51377 Leverkusen, Germany
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2001年 / 50卷 / 01期
关键词
ligase chain reaction; cleavase; colorimetric detection; point mutation detection;
D O I
10.1016/S0165-022X(01)00178-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new method for the identification of point mutations is proposed. The method is based on ligase chain reaction (LCR) and it includes a procedure for correction of ligation by Cleavase. Reaction products are detected by a colorimetric method after adsorption of the resulting DNA duplexes to the solid phase. One strand of LCR products carries biotin to be bound on a streptavidin-coated microwell. Another strand contains a single-stranded region that is to be coupled with an oligonucleotide carrying a substrate for colorimetric detection. The suggested method has two advantages: (i) use of Cleavase increases the accuracy of ligation and (ii) a template independent ligation does not occur in LCR due to a special design of primers. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 89
页数:11
相关论文
共 19 条
[1]   DOT BLOT DETECTION OF POINT MUTATIONS WITH ADJACENTLY HYBRIDIZING SYNTHETIC OLIGONUCLEOTIDE PROBES [J].
ALVES, AM ;
CARR, FJ .
NUCLEIC ACIDS RESEARCH, 1988, 16 (17) :8723-8723
[3]   A METHOD TO DETECT RAS POINT MUTATIONS IN SMALL SUBPOPULATIONS OF CELLS [J].
CHEN, J ;
VIOLA, MV .
ANALYTICAL BIOCHEMISTRY, 1991, 195 (01) :51-56
[4]   DETECTION OF SICKLE-CELL BETA-S-GLOBIN ALLELE BY HYBRIDIZATION WITH SYNTHETIC OLIGONUCLEOTIDES [J].
CONNER, BJ ;
REYES, AA ;
MORIN, C ;
ITAKURA, K ;
TEPLITZ, RL ;
WALLACE, RB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (01) :278-282
[5]   The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation [J].
De Stefano, V ;
Martinelli, I ;
Mannucci, PM ;
Paciaroni, K ;
Chiusolo, P ;
Casorelli, I ;
Rossi, E ;
Leone, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (11) :801-806
[6]   A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].
FROSST, P ;
BLOM, HJ ;
MILOS, R ;
GOYETTE, P ;
SHEPPARD, CA ;
MATTHEWS, RG ;
BOERS, GJH ;
DENHEIJER, M ;
KLUIJTMANS, LAJ ;
VANDENHEUVEL, LP ;
ROZEN, R .
NATURE GENETICS, 1995, 10 (01) :111-113
[7]   DETECTION OF SINGLE DNA-BASE DIFFERENCES BY COMPETITIVE OLIGONUCLEOTIDE PRIMING [J].
GIBBS, RA ;
NGUYEN, PN ;
CASKEY, CT .
NUCLEIC ACIDS RESEARCH, 1989, 17 (07) :2437-2448
[8]  
KHAN SM, 1991, ONCOGENE, V6, P1079
[9]   A LIGASE-MEDIATED GENE DETECTION TECHNIQUE [J].
LANDEGREN, U ;
KAISER, R ;
SANDERS, J ;
HOOD, L .
SCIENCE, 1988, 241 (4869) :1077-1080
[10]   Improving the fidelity of Thermus thermophilus DNA ligase [J].
Luo, JY ;
Bergstrom, DE ;
Barany, F .
NUCLEIC ACIDS RESEARCH, 1996, 24 (15) :3071-3078