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局部诱变:一种在病毒基因组预选区域产生碱基置换的病毒突变体的方法。

Local mutagenesis: a method for generating viral mutants with base substitutions in preselected regions of the viral genome.

作者信息

Shortle D, Nathans D

出版信息

Proc Natl Acad Sci U S A. 1978 May;75(5):2170-4. doi: 10.1073/pnas.75.5.2170.

Abstract

DNA from simian virus 40 (SV40) was prepared for local mutagenesis by nicking the molecule at a specific site with a restriction endonuclease that recognizes one site in SV40 DNA and then extending the nick enzymatically to expose a short, single-stranded segment of DNA. The "gapped" DNA was treated with a single-strand-specific mutagen, sodium bisulfite, which converts cytosine to uracil. After mutagenesis, the gap was repaired with DNA polymerase, generating molecules resistant to the restriction enzyme used to make the initial nick. From cells infected with DNA thus modified, SV40 mutants were isolated that had enzyme-resistant genomes. In some cases, precise positions of G.C to A.T transitions could be inferred from the patterns of susceptibility of mutant DNA to other restriction endonucleases whose recognition sequences were altered by the mutagenesis procedure. One of the restriction endonuclease sites mutagenized (Bgl I) maps at the origin of SV40 DNA replication and near sequences corresponding to the 5' ends of viral mRNAs. Many of the resulting Bgl I-resistant mutants yielded small plaques, suggesting partial defectiveness in DNA replication or transcription.

摘要

猿猴病毒40(SV40)的DNA用于局部诱变,方法是用一种限制性内切酶在特定位点切割分子,该酶识别SV40 DNA中的一个位点,然后通过酶促作用延长切口,以暴露一小段单链DNA。“缺口”DNA用单链特异性诱变剂亚硫酸氢钠处理,亚硫酸氢钠将胞嘧啶转化为尿嘧啶。诱变后,用DNA聚合酶修复缺口,生成对用于产生初始切口的限制性酶具有抗性的分子。从感染了如此修饰的DNA的细胞中,分离出具有酶抗性基因组的SV40突变体。在某些情况下,可以从突变DNA对其他限制性内切酶的敏感性模式推断出G.C到A.T转换的精确位置,这些酶的识别序列因诱变过程而改变。诱变的一个限制性内切酶位点(Bgl I)位于SV40 DNA复制起点,且靠近与病毒mRNA 5'端对应的序列。许多产生的抗Bgl I突变体形成小噬斑,表明在DNA复制或转录方面存在部分缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c4e/392513/d3627adec351/pnas00017-0124-a.jpg

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