Construction and analysis of viable deletion mutants of simian virus 40

Author:

Shenk T E,Carbon J,Berg P

Abstract

Viable mutants of simian virus 40 (SV40), with deletions ranging in size from 15 to 200 base pairs, have been obtained by infecting CV-1P cells with circularly permuted linear SV40 DNA. The linear DNA was produced by cleavage of closed circular DNA with DNase I in the presence of Mn2+, followed, in some cases, by mild digestion with lambda 5'-exonuclease. The SV40 map location and the size of each deletion were determined by using the S1 nuclease mapping procedure (Shenk et al., 1975) and the change in size of fragments produced by Hind II + III endonuclease cleavage. Deletions in at least three regions of the SV40 chromosome have slight or no effect on the rate or yield of viral multiplication and on vira-induced cellular transformation. These regions are located at the following coordinates on the SV40 physical map: 0.17 to 0.18; 0.54 to 0.59; and 0.68 to 0.74.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference22 articles.

1. The gel electrophoresis of DNA;Aaij C.;Biochim. Biophys. Acta,1972

2. Biochemical procedure for production of small deletions in SV40 DNA;Carbon J.;Proc. Natl. Acad. Sci. U.S.A.,1975

3. Specific cleavage of SV40 DNA by restriction endonuclease of Hemophilus influenzae;Danna K.;Proc. Natl. Acad. Sci. U.S.A.,1971

4. A cleavage map of the SV40 genome;Danna K. J.;J. Mol. Biol.,1973

5. Topoinhibition and serum requirement of transformed and untransformed cells;Dulbecco R.;Nature (London),1970

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