Biochemical Method for Mapping Mutational Alterations in DNA with S1 Nuclease: The Location of Deletions and Temperature-Sensitive Mutations in Simian Virus 40

• Published in: Proceedings of the National Academy of Sciences - PNAS 1975-03, Vol.72 (3), p.989-993
• Main Authors: Shenk, Thomas E., Rhodes, Carl, Peter W. J. Rigby, Berg, Paul
• Format: Article
• Language: English
• Subjects: Aspergillus - enzymology; Base Sequence; Binding Sites; Biochemistry; Cell lines; Chromosome Mapping - methods; DNA; DNA mapping; DNA, Single-Stranded - analysis; DNA, Single-Stranded - metabolism; DNA, Viral - analysis; DNA, Viral - metabolism; Gels; Genetic mutation; Hydrolysis; Kidney cells; Molecules; Mutation; Nucleic acid heteroduplexes; Phosphoric Diester Hydrolases - metabolism; Simian virus 40 - analysis; Temperature; Zinc - pharmacology
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.72.3.989

S1 nuclease (EC 3.1.4.X), a single-strand-specific nuclease, can be used to accurately map the location of mutational alterations in simian virus 40 (SV40) DNA. Deletions of between 32 and 190 base pairs, which are at or below the limit of detectability by conventional electron microscopic analysis of heteroduplex DNAs, have been located in this way. To map a deletion, a mixture of unit length, linear DNA, prepared from the SV40 deletion mutant and its wild-type parent, are denatured and reannealed to form heteroduplexes. S1 nuclease can cut such heteroduplexes at the nonbase-paired region to produce fragments whose lengths correspond to the position of the deletion. Similarly, specific fragments are produced when S1 nuclease cleaves a heteroduplex formed from the DNAs of SV40 temperature-sensitive mutants and either their revertants or wild-type parents. Thus, the positions of the nonhomology between these DNAs can be determined.