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Open AccessJournal ArticleDOI

The origin of spontaneous mutation in saccharomyces cerevisiae

Siew-Keen Quah, +2 more
- 01 Dec 1980 - 
- Vol. 96, Iss: 4, pp 819-839
TLDR
An additive effect on the reduction in spontaneous mutation leads to the conclusion that at least 90% of spontaneous mutations seen in the wild type are caused by mutagenic repair of spontaneous lesions.
Abstract
Characterization of two antimutator loci in yeast shows that both are members of the same mutagenic repair system known to be responsible for almost all induced mutation (LAWRENCE and CHRISTENSEN 1976, 1979a,b; PRAKASH 1976). One of the these newly isolated antimutator mutations is an allele of rev3 (LEMONTT 1971b). Two other alleles of rev3 were tested and were also found to be antimutators. Double mutants carrying rev3 and mutator mutations of rad3, rad51 or rad18 are like rev3 single mutants with respect to spontaneous mutation rate, supporting the hypothesis (HASTINGS, QUAH and VON BORSTEL, 1976) that many mutators in yeast act by channelling spontaneous lesions from accurate to mutagenic repair. However, the enhanced mutation rate seen in a radiation-resistant mutator mutant mut1 is not dependent on REV3, but is dependent on another gene designated ANT1. An additive effect on the reduction in spontaneous mutation, seen in the ant1 rev3 double-mutant strain, leads to the conclusion that at least 90% of spontaneous mutations seen in the wild type are caused by mutagenic repair of spontaneous lesions.

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Citations
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Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan

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Control of spontaneous and damage-induced mutagenesis by SUMO and ubiquitin conjugation

TL;DR: These findings assign a function to SUMO during S phase and demonstrate how ubiquitin and SUMO, by regulating the accuracy of replication and repair, contribute to overall genomic stability.
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Xeroderma pigmentosum variant (XP-V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity.

TL;DR: A sensitive assay system is established using an SV40 origin‐based plasmid to detect XP‐V complementation activity and isolated a protein from HeLa cells capable of complementing the defects inXP‐V cell extracts that corrected the translesion defects of extracts from three XPV cell strains.
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Mutagenesis in Mammalian Cells Induced by Triple Helix Formation and Transcription-Coupled Repair

TL;DR: When mammalian cells were treated with triplex-forming oligonucleotides of sufficient binding affinity, mutations were specifically induced in a simian virus 40 vector contained within the cells, raising the possibility that naturally occurring triple helices are a source of genetic instability.
References
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Journal ArticleDOI

Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae

TL;DR: In isolated mutants sensitive to methyl methanesulfonate (MMS) in Saccharomyces cerevisiae, the cross-sensitivities of these mms mutants to UV and X rays are discussed in terms of their possible involvement in DNA repair.
Journal ArticleDOI

Mutants of Yeast Sensitive to Ultraviolet Light

TL;DR: Six uvr mutants of Saccharomyces cerevisiae with hypersensitivity to ultraviolet (UV) light were isolated after mutagen treatment with ethylmethanesulfonate and implementation tests and tetrad analysis indicate that each strain represents mutation in a different gene.
Journal ArticleDOI

Effect of Genes Controlling Radiation Sensitivity on Chemically Induced Mutations in SACCHAROMYCES CEREVISIAE.

TL;DR: The effect of 16 different genes (rad) conferring radiation sensitivity on chemically induced reversion in the yeast Saccharomyces cerevisiae was determined in this paper, where the site of reversion used was a well-defined chain initiation mutant mapping in the structural gene coding for iso-1-cytochrome c.
Journal ArticleDOI

Ultraviolet-induced reversion of cyc1 alleles in radiation-sensitive strains of yeast: I. rev1 mutant strains☆

TL;DR: The evidence of this kind of allele-specific control of u.v. -induced reversion must be accounted for by any proposed model of the mutagenic process and must also be accommodated by any scheme to test environmental mutagens.
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