DETECTION OF MUTATIONS BY CLEAVAGE OF DNA HETERODUPLEXES WITH BACTERIOPHAGE RESOLVASES

被引:191
作者
MASHAL, RD [1 ]
KOONTZ, J [1 ]
SKLAR, J [1 ]
机构
[1] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV MED ONCOL,BOSTON,MA 02115
关键词
D O I
10.1038/ng0295-177
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have explored the application of the bacteriophage resolvases T4 endonuclease VII and T7 endonuclease I for detecting mutations in genomic DNA. Heteroduplex DNA fragments prepared by amplification from DNA containing known mutations were cleaved by one or both enzymes at nucleotide mismatches created by 3 of 3 short deletions and 13 of 14 point mutations in fragments as large as 940 basepairs. Heteroduplexes representing all four classes of possible single nucleotide mismatches were cleaved, and the sizes of the cleavage products generated correlated with the location of the mutation. We conclude that bacteriophage resolvases may be useful reagents for the rapid screening of DNA for mutations.
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页码:177 / 183
页数:7
相关论文
共 23 条
[1]   CURRENT METHODS OF MUTATION DETECTION [J].
COTTON, RGH .
MUTATION RESEARCH, 1993, 285 (01) :125-144
[2]  
DAVIDOW LS, 1992, COMPUT APPL BIOSCI, V8, P193
[3]   TOUCHDOWN PCR TO CIRCUMVENT SPURIOUS PRIMING DURING GENE AMPLIFICATION [J].
DON, RH ;
COX, PT ;
WAINWRIGHT, BJ ;
BAKER, K ;
MATTICK, JS .
NUCLEIC ACIDS RESEARCH, 1991, 19 (14) :4008-4008
[4]  
ELLIS LA, 1994, NUCLEIC ACIDS RES, V2, P2710
[5]   CONFORMATION-SENSITIVE GEL-ELECTROPHORESIS FOR RAPID DETECTION OF SINGLE-BASE DIFFERENCES IN DOUBLE-STRANDED PCR PRODUCTS AND DNA FRAGMENTS - EVIDENCE FOR SOLVENT-INDUCED BENDS IN DNA HETERODUPLEXES [J].
GANGULY, A ;
ROCK, MJ ;
PROCKOP, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (21) :10325-10329
[6]   DETECTION OF SINGLE-BASE MUTATIONS BY REACTION OF DNA HETERODUPLEXES WITH A WATER-SOLUBLE CARBODIIMIDE FOLLOWED BY PRIMER EXTENSION - APPLICATION TO PRODUCTS FROM THE POLYMERASE CHAIN-REACTION [J].
GANGULY, A ;
PROCKOP, DJ .
NUCLEIC ACIDS RESEARCH, 1990, 18 (13) :3933-3939
[7]   IDENTIFICATION AND CHARACTERIZATION OF THE FAMILIAL ADENOMATOUS POLYPOSIS-COLI GENE [J].
GRODEN, J ;
THLIVERIS, A ;
SAMOWITZ, W ;
CARLSON, M ;
GELBERT, L ;
ALBERTSEN, H ;
JOSLYN, G ;
STEVENS, J ;
SPIRIO, L ;
ROBERTSON, M ;
SARGEANT, L ;
KRAPCHO, K ;
WOLFF, E ;
BURT, R ;
HUGHES, JP ;
WARRINGTON, J ;
MCPHERSON, J ;
WASMUTH, J ;
LEPASLIER, D ;
ABDERRAHIM, H ;
COHEN, D ;
LEPPERT, M ;
WHITE, R .
CELL, 1991, 66 (03) :589-600
[8]   THE RAPID DETECTION OF UNKNOWN MUTATIONS IN NUCLEIC-ACIDS [J].
GROMPE, M .
NATURE GENETICS, 1993, 5 (02) :111-117
[9]   MISMATCH-CONTAINING OLIGONUCLEOTIDE DUPLEXES BOUND BY THE ESCHERICHIA-COLI MUTS-ENCODED PROTEIN [J].
JIRICNY, J ;
SU, SS ;
WOOD, SG ;
MODRICH, P .
NUCLEIC ACIDS RESEARCH, 1988, 16 (16) :7843-7853
[10]  
KEMPER B, 1981, EUR J BIOCHEM, V115, P123