A study of side reactions occurring during synthesis of oligodeoxynucleotides containing O6-alkyldeoxyguanosine residues at preselected sites.

A study of side reactions occurring during synthesis of oligodeoxynucleotides containing O6-alkyldeoxyguanosine residues at preselected sites.
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研究在预选位点合成含有 O6-烷基脱氧鸟苷残基的寡脱氧核苷酸过程中发生的副反应。

DOI:
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发表时间:
1987
期刊:
影响因子:
2.9
通讯作者:
R. Chambers
R. Chambers
中科院分区:
生物学3区
文献类型:
--
作者:
H. Borowy‐Borowski;R. Chambers

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作为致癌物致突变分子机制研究的一部分,我们合成了12个在预选位置含有O6-烷基鸟嘌呤残基的寡核苷酸(15-MERS),用于酶法合成具有生物活性的DNA。这些寡核苷酸中有10个来自负链序列,该负链序列携带噬菌体Phi x174 DNA的基因G的第三密码子中的修饰核苷酸。另外两个来自携带人类Ha-ras原癌基因第12密码子修饰的正链序列。在这项工作中,观察到了几个潜在的严重副反应,这可能会使突变数据的解释复杂化。本文对这些反应进行了详细的研究。由于我们无法避免不受欢迎的副产品,我们开发了简单的层析方法来检测和去除它们。
As part of our studies on the molecular mechanisms of mutation by carcinogens we have synthesized 12 oligonucleotides (15-mers) containing an O6-alkylguanine residue at a preselected position for use as primers in the enzymatic synthesis of biologically active DNA. Ten of these oligonucleotides are derived from a minus strand sequence carrying the modified nucleotide in the third codon of gene G of bacteriophage phi X174 DNA. Two others are derived from plus strand sequences carrying the modification in the 12th codon of the human Ha-ras protooncogene. During this work several potentially serious side reactions, which could complicate interpretation of mutagenesis data, were observed. This paper describes a detailed study of these reactions. Since we were unable to avoid undesirable side products, we developed simple chromatographic methods for detecting and removing them.
DOI: 10.1093/nar/11.10.3393
发表时间: 1983
影响因子: 14.9
作者:
Kuzmich,S;Marky,LA;Jones,RA
通讯作者: Jones,RA
DOI: --
发表时间: 1986
期刊: The Journal of biological chemistry
影响因子: --
作者:
Topal,MD;Eadie,JS;Conrad,M
通讯作者: Conrad,M