Procedure for Identifying Nonsense Mutations

Author:

Berkowitz David1,Hushon Judith M.1,Whitfield Harvey J.1,Roth John1,Ames Bruce N.1

Affiliation:

1. Laboratory of Molecular Biology, National Institute of Arthritis and Metabolic Diseases, Bethesda, Maryland 20014

Abstract

A method has been devised for the rapid identification of nonsense mutations (UAG, UAA, UGA codons) in Salmonella . The mutations to be tested are reverted, and the revertants are replica-printed onto lactose plates spread with lawns of tester strains. These tester strains contain F′ lac episomes with nonsense mutations in the episomal Z gene. The revertants are infected with the episome from the tester strain lawn. Because S. typhimurium is unable to ferment lactose, only those revertants which have nonsense suppressors are able to grow on lactose. If colonies appear on the lactose plate, it may be concluded that the original strain carries a nonsense mutation, since nonsense suppressors suppress the mutant phenotype.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference21 articles.

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2. Frameshift mutagenesis in Salmonella;Ames B. N.;Cold Spring Harbor Symp. Quant. Biol.,1966

3. Altered amino acid sequences produced by reversion of frameshift mutants of tryptophan synthetase A gene of E. coli;Brammar W. J.;Proc. Natl. Acad. Sci. U.,1967

4. UGA: a third nonsense triplet in the genetic code;Brenner S.;Nature,1967

5. Ochre mutants, a new class of suppressible nonsense mutants;Brenner S.;J. Mol. Biol.,1965

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