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由寡核苷酸的磷酸三酯类似物指导的诱变:一种体内位点特异性诱变的方法。

Mutagenesis directed by phosphotriester analogues of oligonucleotides: a way to site-specific mutagenesis in vivo.

作者信息

Petrenko V A, Kipriyanov S M, Boldyrev A N, Pozdnyakov P I

机构信息

All-Union Institute of Molecular Biology, Kol'tsovo, Novosibirsk Region, USSR.

出版信息

FEBS Lett. 1988 Sep 26;238(1):109-12. doi: 10.1016/0014-5793(88)80236-9.

DOI:10.1016/0014-5793(88)80236-9
PMID:3049154
Abstract

A new approach to induce directed mutations in genes of study through simple cotransfection of E. coli cells by the mixture of primer and template was developed. This method is based on the use of synthetic phosphotriester analogues of oligonucleotides as site-specific mutagenic primers. The achieved yield of mutant clones was 2-3%.

摘要

通过将引物和模板的混合物简单共转染大肠杆菌细胞,开发出了一种在研究基因中诱导定向突变的新方法。该方法基于使用寡核苷酸的合成磷酸三酯类似物作为位点特异性诱变引物。获得的突变克隆产率为2%-3%。

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1
Mutagenesis directed by phosphotriester analogues of oligonucleotides: a way to site-specific mutagenesis in vivo.由寡核苷酸的磷酸三酯类似物指导的诱变:一种体内位点特异性诱变的方法。
FEBS Lett. 1988 Sep 26;238(1):109-12. doi: 10.1016/0014-5793(88)80236-9.
2
[Mutagenesis directed by phosphotriester analogs of oligonucleotides: a way to site-specific mutagenesis in vivo].[由寡核苷酸的磷酸三酯类似物指导的诱变:一种体内位点特异性诱变的方法]
Mol Gen Mikrobiol Virusol. 1989 Mar(3):35-9.
3
Oligonucleotide-directed mutagenesis: a simple method using two oligonucleotide primers and a single-stranded DNA template.寡核苷酸定向诱变:一种使用两个寡核苷酸引物和单链DNA模板的简单方法。
Methods Enzymol. 1987;154:329-50. doi: 10.1016/0076-6879(87)54083-6.
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Oligonucleotide-directed mutagenesis using M13-derived vectors: an efficient and general procedure for the production of point mutations in any fragment of DNA.使用M13衍生载体的寡核苷酸定向诱变:在任何DNA片段中产生点突变的高效通用方法。
Nucleic Acids Res. 1982 Oct 25;10(20):6487-500. doi: 10.1093/nar/10.20.6487.
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Oligonucleotide-directed mutagenesis: a simple method using two oligonucleotide primers and a single-stranded DNA template.寡核苷酸定向诱变:一种使用两条寡核苷酸引物和单链DNA模板的简单方法。
DNA. 1984 Dec;3(6):479-88. doi: 10.1089/dna.1.1984.3.479.
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Induction of multiple replacement mutations by oligonucleotide-directed mutagenesis with extended mismatch primers.
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Oligonucleotide-directed construction of mutations via gapped duplex DNA.通过缺口双链DNA进行寡核苷酸定向突变构建
Methods Enzymol. 1987;154:350-67. doi: 10.1016/0076-6879(87)54084-8.
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Saturation mutagenesis using mixed oligonucleotides and M13 templates containing uracil.
Methods Enzymol. 1990;185:599-611. doi: 10.1016/0076-6879(90)85047-r.
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[Mutagenesis, induced by phosphotriester analogs of oligonucleotides and directed to the cleavage site of double-spiral DNA].[由寡核苷酸的磷酸三酯类似物诱导并靶向双螺旋DNA切割位点的诱变作用]
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The gapped duplex DNA approach to oligonucleotide-directed mutation construction.用于寡核苷酸定向突变构建的缺口双链DNA方法。
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