DETECTION OF POINT MUTATIONS IN THE P53 GENE - COMPARISON OF SINGLE-STRAND CONFORMATION POLYMORPHISM, CONSTANT DENATURANT GEL-ELECTROPHORESIS, AND HYDROXYLAMINE AND OSMIUM-TETROXIDE TECHNIQUES

被引:110
作者
CONDIE, A
EELES, R
BORRESEN, AL
COLES, C
COOPER, C
PROSSER, J
机构
[1] WESTERN GEN HOSP,MRC,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
[2] ROYAL MARSDEN HOSP,ACAD UNIT RADIOTHERAPY,SUTTON SM2 5NG,SURREY,ENGLAND
[3] ROYAL MARSDEN HOSP,INST CANC RES,SUTTON SM2 5NG,SURREY,ENGLAND
[4] NORWEGIAN RADIUM HOSP,INST CANC RES,DEPT GENET,N-0310 OSLO 3,NORWAY
关键词
POINT MUTATION; P53; SSCP; CDGE; HOT; CHEMICAL MISMATCH;
D O I
10.1002/humu.1380020111
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A comparison was made between the 3 most commonly used techniques for the detection of point mutations: single-strand conformation polymorphism (SSCP), constant denaturant gel electrophoresis (CDGE), and hydroxylamine and osmium tetroxide used in amplification mismatch cleavage analysis (HOT). Using human DNA samples containing known mutations in the p53 gene, SSCP detected 90% of mutations (18/20), CDGE detected 88% (15/17) pre-decoding of the samples but 100% when the mutations were known and the CDGE conditions optimized, and the HOT technique was 100% accurate, although 1 mutation was missed through careless examination of the gel. The positive and negative aspects of each of the techniques are considered and suggestions are made regarding the particular situations in which each of them is most useful.
引用
收藏
页码:58 / 66
页数:9
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