Colourimetric point mutation assay: For detection of precore mutants of hepatitis B

被引:14
作者
Ballard, AL
Boxall, EH
机构
[1] Public Health Laboratory, Birmingham Heartlands Solihull NHS, Heartlands Hospital, Birmingham B9 5SS, Bordesley Green East
关键词
precore mutation; PCR; point mutation; hepatitis B;
D O I
10.1016/S0166-0934(97)00089-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A colourimetric assay for the analysis of point mutations in PCR amplified DNA fragments from hepatitis B virus (HBV is described. The method was applied for analysis of the single point mutation in codon 28 of the precore gene of HBV, which inhibits expression of HBe antigen. The assay, which uses a microtitre plate formal, incorporates fluorscein-labelled dideoxynucleotides as opposed to radioactively-labelled deoxynucleotides used in methods described previously. Synthetic control wild type and mutant oligonucleotides were tested to optimise the reaction conditions. The assay was thus shown to yield both qualitative and quantitative data on the relative proportions of wild type and mutant sequences within a given sample. Amplicons from clinical specimens of known sequence were analysed to validate the assay. Sixteen chronic carriers of HBV were tested using the codon 28 point mutation assay, and the results were confirmed by direct sequencing. The method described is suitable for applications where point mutations are of interest. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:143 / 152
页数:10
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