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猿猴病毒40的存活缺失突变体:通过副流感嗜血杆菌的限制性内切酶进行选择性分离

Viable deletion mutants of simian virus 40: selective isolation by means of a restriction endonuclease from Hemophilus parainfluenzae.

作者信息

Mertz J E, Berg P

出版信息

Proc Natl Acad Sci U S A. 1974 Dec;71(12):4879-83. doi: 10.1073/pnas.71.12.4879.

Abstract

Resistance of simian virus 40 (SV40) DNA to cleavage by Hemophilus parainfluenzae II (HpaII) restriction endonuclease has been used as a positive, in vitro selection for mutants lacking the one HpaII endonuclease-cleavage site of wild-type SV40 DNA. Each of 10 viable mutants isolated by this procedure multiplies significantly more slowly than wild-type virus and contains a small deletion (80 to 190 base pairs in size) of the region of the genome that includes the HpaII endonuclease-recognition sequence. These well-defined mutants, having a selective disadvantage for growth, would not have been readily obtained by conventional methods used to screen for viral mutants. Therefore, in certain circumstances, restriction endonucleases are effective reagents for the selection of new classes of mutants. Because these small deletions can be visualized in heteroduplexes, these mutants provide internal markers for mapping other alterations or features of the simian virus 40 genome.

摘要

猴空泡病毒40(SV40)DNA对副流感嗜血杆菌II(HpaII)限制性内切酶切割的抗性已被用作一种阳性的体外筛选方法,用于筛选缺乏野生型SV40 DNA的一个HpaII内切酶切割位点的突变体。通过该方法分离出的10个存活突变体中的每一个,其增殖速度都比野生型病毒慢得多,并且在基因组中包含HpaII内切酶识别序列的区域有一个小的缺失(大小为80至190个碱基对)。这些定义明确的突变体在生长方面具有选择性劣势,通过用于筛选病毒突变体的传统方法不容易获得。因此,在某些情况下,限制性内切酶是选择新型突变体的有效试剂。由于这些小的缺失可以在异源双链体中可视化,这些突变体为绘制猴空泡病毒40基因组的其他改变或特征提供了内部标记。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc7/434002/57b3b99f6112/pnas00075-0242-a.jpg

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