Oligonucleotide ligation assay-based DNA chip for multiplex detection of single nucleotide polymorphism

被引:34
作者
Deng, HY
Zhang, XE [1 ]
Mang, Y
Zhang, ZP
Zhou, YF
Liu, Q
Lu, HB
Fu, ZJ
机构
[1] Chinese Acad Sci, Wuhan Inst Virol, Wuhan 430071, Peoples R China
[2] Chinese Acad Sci, Wuhan Inst Hydrobiol, Wuhan 430072, Peoples R China
[3] Wuhan TB Prevent & Cure Inst, Wuhan 430030, Peoples R China
关键词
oligonucleotide ligation assay; DNA chip; single nucleotide polymorphism detection; T4 DNA ligase; pentamer; enzyme-linked assay; M; tuberculosis;
D O I
10.1016/j.bios.2003.11.022
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
An oligonucleotide ligation assay-based DNA chip has been developed to detect single nucleotide polymorphism. Synthesized nonamers, complementary to the flanking sequences of the mutation sites in target DNA, were immobilized onto glass slides through disulfide bonds on their 5' terminus. Allele-specific pentamers annealed adjacent to the nonamers on the complementary target DNA, containing 5'-phosphate groups and biotin labeled 3'-ends, were mixed with the target DNA in tube. Ligation reactions between nonamers and pentamers were carried out on chips in the presence of T4 DNA ligase. Ligation products were directly visualized on chips through enzyme-linked assay. The effect of G:T mismatch at different positions of pentamers on the ligation were evaluated. The results showed that any mismatch between pentamer and the target DNA could lead to the decrease of ligation, which can be detected easily. The established approach was further used for multiplex detection of mutations in rpoB gene of rifampin-resistant Mycobacterium tuberculosis clinical isolates. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:1277 / 1283
页数:7
相关论文
共 31 条
[2]  
Bernardino Andrea L Ferreira, 2003, JOP, V4, P169
[3]  
Bonadona V, 2003, B CANCER, V90, P587
[4]   PCR AMPLIFICATION OF SPECIFIC ALLELES - RAPID DETECTION OF KNOWN MUTATIONS AND POLYMORPHISMS [J].
BOTTEMA, CDK ;
SOMMER, SS .
MUTATION RESEARCH, 1993, 288 (01) :93-102
[5]   A homogeneous, ligase-mediated DNA diagnostic test [J].
Chen, XN ;
Livak, KJ ;
Kwok, PY .
GENOME RESEARCH, 1998, 8 (05) :549-556
[6]   REACTIVITY OF CYTOSINE AND THYMINE IN SINGLE-BASE-PAIR MISMATCHES WITH HYDROXYLAMINE AND OSMIUM-TETROXIDE AND ITS APPLICATION TO THE STUDY OF MUTATIONS [J].
COTTON, RGH ;
RODRIGUES, NR ;
CAMPBELL, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (12) :4397-4401
[7]   Fractionation, phosphorylation and ligation on oligonucleotide microchips to enhance sequencing by hybridization [J].
Dubiley, S ;
Kirillov, E ;
Lysov, Y ;
Mirzabekov, A .
NUCLEIC ACIDS RESEARCH, 1997, 25 (12) :2259-2265
[8]   16S rRNA mutation-mediated tetracycline resistance in Helicobacter pylori [J].
Gerrits, MM ;
de Zoete, MR ;
Arents, NLA ;
Kuipers, EJ ;
Kusters, JG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (09) :2996-3000
[9]   Alterations in penicillin-binding protein 1A confer resistance to β-lactam antibiotics in Helicobacter pylori [J].
Gerrits, MM ;
Schuijffel, D ;
van Zwet, AA ;
Kuipers, EJ ;
Vandenbroucke-Grauls, CMJE ;
Kusters, JG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (07) :2229-2233
[10]   Universal DNA microarray method for multiplex detection of low abundance point mutations [J].
Gerry, NP ;
Witowski, NE ;
Day, J ;
Hammer, RP ;
Barany, G ;
Barany, F .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 292 (02) :251-262