Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast.

Complex traits typically involve the contribution of multiple gene variants. In this study, we took advantage of a high-density genotyping analysis of the BY (S288c) and RM strains of Saccharomyces cerevisiae and of 123 derived spore progeny to identify the genetic loci that underlie a complex DNA r...

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Main Authors: Ann Demogines, Erin Smith, Leonid Kruglyak, Eric Alani
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-07-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC2440805?pdf=render
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spelling doaj-dd26f7efef3646c2b73c56ad63ea65fd2020-11-24T21:56:53ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042008-07-0147e100012310.1371/journal.pgen.1000123Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast.Ann DemoginesErin SmithLeonid KruglyakEric AlaniComplex traits typically involve the contribution of multiple gene variants. In this study, we took advantage of a high-density genotyping analysis of the BY (S288c) and RM strains of Saccharomyces cerevisiae and of 123 derived spore progeny to identify the genetic loci that underlie a complex DNA repair sensitivity phenotype. This was accomplished by screening hybrid yeast progeny for sensitivity to a variety of DNA damaging agents. Both the BY and RM strains are resistant to the ultraviolet light-mimetic agent 4-nitroquinoline 1-oxide (4-NQO); however, hybrid progeny from a BYxRM cross displayed varying sensitivities to the drug. We mapped a major quantitative trait locus (QTL), RAD5, and identified the exact polymorphism within this locus responsible for 4-NQO sensitivity. By using a backcrossing strategy along with array-assisted bulk segregant analysis, we identified one other locus, MKT1, and a QTL on Chromosome VII that also link to the hybrid 4-NQO-sensitive phenotype but confer more minor effects. This work suggests an additive model for sensitivity to 4-NQO and provides a strategy for mapping both major and minor QTL that confer background-specific phenotypes. It also provides tools for understanding the effect of genetic background on sensitivity to genotoxic agents.http://europepmc.org/articles/PMC2440805?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ann Demogines
Erin Smith
Leonid Kruglyak
Eric Alani
spellingShingle Ann Demogines
Erin Smith
Leonid Kruglyak
Eric Alani
Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast.
PLoS Genetics
author_facet Ann Demogines
Erin Smith
Leonid Kruglyak
Eric Alani
author_sort Ann Demogines
title Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast.
title_short Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast.
title_full Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast.
title_fullStr Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast.
title_full_unstemmed Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast.
title_sort identification and dissection of a complex dna repair sensitivity phenotype in baker's yeast.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2008-07-01
description Complex traits typically involve the contribution of multiple gene variants. In this study, we took advantage of a high-density genotyping analysis of the BY (S288c) and RM strains of Saccharomyces cerevisiae and of 123 derived spore progeny to identify the genetic loci that underlie a complex DNA repair sensitivity phenotype. This was accomplished by screening hybrid yeast progeny for sensitivity to a variety of DNA damaging agents. Both the BY and RM strains are resistant to the ultraviolet light-mimetic agent 4-nitroquinoline 1-oxide (4-NQO); however, hybrid progeny from a BYxRM cross displayed varying sensitivities to the drug. We mapped a major quantitative trait locus (QTL), RAD5, and identified the exact polymorphism within this locus responsible for 4-NQO sensitivity. By using a backcrossing strategy along with array-assisted bulk segregant analysis, we identified one other locus, MKT1, and a QTL on Chromosome VII that also link to the hybrid 4-NQO-sensitive phenotype but confer more minor effects. This work suggests an additive model for sensitivity to 4-NQO and provides a strategy for mapping both major and minor QTL that confer background-specific phenotypes. It also provides tools for understanding the effect of genetic background on sensitivity to genotoxic agents.
url http://europepmc.org/articles/PMC2440805?pdf=render
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