Lis ET~Romesberg FE, 2008

Pubmed ID 18400565
Title Identification of pathways controlling DNA damage induced mutation in Saccharomyces cerevisiae.
Authors Ewa T Lis, Bryan M O'Neill, Cristina Gil-Lamaignere, Jodie K Chin, Floyd E Romesberg
Abstract Mutation in response to most types of DNA damage is thought to be mediated by the error-prone sub-branch of post-replication repair and the associated translesion synthesis polymerases. To further understand the mutagenic response to DNA damage, we screened a collection of 4848 haploid gene deletion strains of Saccharomyces cerevisiae for decreased damage-induced mutation of the CAN1 gene. Through extensive quantitative validation of the strains identified by the screen, we identified ten genes, which included error-prone post-replication repair genes known to be involved in induced mutation, as well as two additional genes, FYV6 and RNR4. We demonstrate that FYV6 and RNR4 are epistatic with respect to induced mutation, and that they function, at least partially, independently of post-replication repair. This pathway of induced mutation appears to be mediated by an increase in dNTP levels that facilitates lesion bypass by the replicative polymerase Pol delta, and it is as important as error-prone post-replication repair in the case of UV- and MMS-induced mutation, but solely responsible for EMS-induced mutation. We show that Rnr4/Pol delta-induced mutation is efficiently inhibited by hydroxyurea, a small molecule inhibitor of ribonucleotide reductase, suggesting that if similar pathways exist in human cells, intervention in some forms of mutation may be possible.
Citation DNA Repair (Amst.) 2008; 7:801-10

Datasets

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Paper Phenotype Condition Reference Collection Tested mutants Data Details
Lis ET~Romesberg FE, 2008 mutation frequency (CanR) ultraviolet light [50 J/m2] hap a ~4,848 Quantitative only for hits
Lis ET~Romesberg FE, 2008 mutation frequency (CanR) standard hap a ~4,848 Quantitative only for hits

Curation history

Tested strains

Oct. 18, 2016 To request.
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Data

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