Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1982;187(1):42-6.
doi: 10.1007/BF00384381.

New temperature-sensitive mutants of Saccharomyces cerevisiae affecting DNA replication

New temperature-sensitive mutants of Saccharomyces cerevisiae affecting DNA replication

L B Dumas et al. Mol Gen Genet. 1982.

Abstract

We have isolated new mutants of the yeast Saccharomyces cerevisiae that are defective in mitotic DNA synthesis. This was accomplished by directly screening 11000 newly isolated temperature-sensitive yeast clones for DNA synthesis defects. Ninety-seven different mutant strains were identified. Approximately half had the fast-stop DNA synthesis phenotype; synthesis ceased quickly after shifting an asynchronous population of cells to the restrictive temperature. The other half had an intermediate-rate phenotype; synthesis continued at a reduced rate for at least 3 h at the restrictive temperature. All of the DNA synthesis mutants continued protein synthesis at the restrictive temperature. Genetic complementation analysis of temperature-sensitive segregants of these strains defined 60 apparently new complementation groups. Thirty-five of these were associated with the fast-stop phenotype, 25 with the intermediate-rate phenotype. The fast-stop groups are likely to include many genes whose products play direct roles in mitotic S phase DNA synthesis. Some of the intermediate-rate groups may be associated with S phase as well. This mutant collection should be very useful in the identification and isolation of gene products necessary for yeast DNA synthesis, in the isolation of the genes themselves, and in further analysis of the DNA replication process in vivo.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Proc Natl Acad Sci U S A. 1981 Dec;78(12):7261-5 - PubMed
    1. J Mol Biol. 1974 Apr 15;84(3):445-61 - PubMed
    1. J Bacteriol. 1967 May;93(5):1662-70 - PubMed
    1. Bacteriol Rev. 1974 Jun;38(2):164-98 - PubMed
    1. J Bacteriol. 1973 Sep;115(3):966-74 - PubMed

Publication types

LinkOut - more resources