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Journal ArticleDOI

Mutants of yeast defective in mutation induced by ultraviolet light.

Jeffrey F. Lemontt
- 01 May 1971 - 
- Vol. 68, Iss: 1, pp 21-33
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TLDR
To identify new genes controlling UV-induced mutation, it is desirable to select strains directly for defective mutation induction, thereby avoiding the prior condition that all such mutants be UV-sensitive.
Abstract
NDUCED mutations are thought to arise as a result of enzymatic processes uti‘lizing DNA damage as a substrate (BRIDGES 1969). Although the molecular mechanism is not known, evidence reviewed by WITKIN (1969) suggests that in E. coli mutations are produced during postreplication repair of lethal damage induced by ultraviolet light (UV) and controlled by r e d and ezrf (or lexf) genes. Strains carrying rec or ezr, although normal in excision repair, exhibit reduced or no UV mutability compared to wild type. In addition, such strains are UV sensitive, X-ray sensitive, and recombination deficient in varying degrees ( WITKIN 1969). In previous studies of UV-induced mutation in fungi, UV-sensitive strains have been selected on the assumption that UV mutagenesis might be related to dark repair of lethal damage. In some of these UV-sensitive strains, the frequencies of UV mutation are reduced compared to wild type at equal UV doses (CHANG, LENNOX and TUVESON 1968; NASIM 1968; WOHLRAB and TUVESON 1969). whereas in others these frequencies are enhanced (AVERBECK et al. 1970; RESNICK 1969; ZAKHAROV, KOZINA and FEDOROVA, 1970). To identify new genes controlling UV-induced mutation, it is desirable to select strains directly for defective mutation induction, thereby avoiding the prior condition that all such mutants be UV-sensitive. Mutants of Saccharomyces cereuisiae were selected ( LEMONTT and MORTIMER 1970) for reduced ability to undergo UV-induced locus reversion of the ochresuppressible (GILMORE 1967; HAWTHORNE 1969) argl-17 allele. This paper describes the isolation and some characteristics of these “reversionless” mutants, The results are discussed in relation to current ideas about induced mutagenesis.

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Journal ArticleDOI

Y-family DNA polymerases and their role in tolerance of cellular DNA damage

TL;DR: The past 15 years have seen an explosion in understanding of how cells replicate damaged DNA and how this can lead to mutagenesis, and the Y-family DNA polymerases lie at the heart of this process, which is commonly known as translesion synthesis.
Journal ArticleDOI

Eukaryotic Translesion Polymerases and Their Roles and Regulation in DNA Damage Tolerance

TL;DR: The current state of knowledge about the eukaryotic DNA damage tolerance pathway translesion synthesis (TLS), a process in which specialized DNA polymerases replicate across from DNA lesions, is summarized.
Journal ArticleDOI

DNA polymerases and cancer

TL;DR: There are 15 different DNA polymerases encoded in mammalian genomes, which are specialized for replication, repair or the tolerance of DNA damage, and some of these enzymes might be viable targets for therapeutic strategies.
Journal ArticleDOI

A genetic study of x-ray sensitive mutants in yeast.

TL;DR: Examination of the survival responses of multiple-mutant strains indicated a minimum of two pathways in the repair of X-ray damage, and a number of the mutants have been mapped and these were found to be dispersed over the genome.
Journal ArticleDOI

Genetic map of Saccharomyces cerevisiae.

R K Mortimer, +1 more
TL;DR: Although all of the data presented in this article are from tetrad analyses, many other techniques have been used to assign genes to chromosomes or to specific chromosome arms, including aneuploid analysis, mitotic recombination analysis,Mitotic chromosome loss or nondisjunction, and random spore analysis.
References
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Journal ArticleDOI

Genetic Mapping in Saccharomyces

R. K. Mortimer, +1 more
- 01 Jan 1966 - 
Journal ArticleDOI

Cytoplasmic and nuclear genetic events induced by UV light in strains of Saccharomyces cerevisiae with different UV sensitivites

E. Moustacchi
- 01 Mar 1969 - 
TL;DR: If the cytoplasmic factor is equated with the mitochondrial DNA, these results may suggest that the fraction of the mitochondrial population, genetically active, is not susceptible to the repair system which is operative for the nuclear events studied.
Journal ArticleDOI

Allelic mapping in yeast by x-ray-induced mitotic reversion.

TL;DR: A new method for determining the sequence of mutational sites is based on the linear dose-effect relation for x-ray induction of allelic recombination in Saccharomyces cerevisiae and maps at two loci have been mapped.
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