DNA repair gene PSO3 of Saccharomyces cerevisiae belongs to the RAD3 epistasis group

The mutant allele pso3-1 of Saccharomyces cerevisiae confers sensitivity to treatment with UV365nm (UVA) light-activated mono- and bi-functional psoralens. When pso3-1 is combined in double mutants with selected rad and pso mutant alleles and subjected to 8-MOP + UVA treatment, epistatic interaction...

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Veröffentlicht in:Current genetics 1992, Vol.21 (1), p.85-90
Hauptverfasser: Benfato, M.S, Brendel, M, Henriques, J.A.P
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creator Benfato, M.S
Brendel, M
Henriques, J.A.P
description The mutant allele pso3-1 of Saccharomyces cerevisiae confers sensitivity to treatment with UV365nm (UVA) light-activated mono- and bi-functional psoralens. When pso3-1 is combined in double mutants with selected rad and pso mutant alleles and subjected to 8-MOP + UVA treatment, epistatic interaction with regard to survival is observed with pso1, pso2, and rad3. With the same treatment the combination of pso3-1 with rad6 and rad52 leads to synergistic interaction. For the monofunctional agent 3-carbethoxypsoralen (3-CPs) the analysis of double mutants yields the same results as with the bifunctional 8-methoxypsoralen (8-MOP) with the exception of the pso1-1pso3-1 double mutant. Here we find an additive interaction, i.e., the sensitivities of both parental strains are summed in the double mutant, which indicates a different substrate specificity of the repair activity encoded by the PSO1 and PSO3 genes.
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When pso3-1 is combined in double mutants with selected rad and pso mutant alleles and subjected to 8-MOP + UVA treatment, epistatic interaction with regard to survival is observed with pso1, pso2, and rad3. With the same treatment the combination of pso3-1 with rad6 and rad52 leads to synergistic interaction. For the monofunctional agent 3-carbethoxypsoralen (3-CPs) the analysis of double mutants yields the same results as with the bifunctional 8-methoxypsoralen (8-MOP) with the exception of the pso1-1pso3-1 double mutant. 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When pso3-1 is combined in double mutants with selected rad and pso mutant alleles and subjected to 8-MOP + UVA treatment, epistatic interaction with regard to survival is observed with pso1, pso2, and rad3. With the same treatment the combination of pso3-1 with rad6 and rad52 leads to synergistic interaction. For the monofunctional agent 3-carbethoxypsoralen (3-CPs) the analysis of double mutants yields the same results as with the bifunctional 8-methoxypsoralen (8-MOP) with the exception of the pso1-1pso3-1 double mutant. Here we find an additive interaction, i.e., the sensitivities of both parental strains are summed in the double mutant, which indicates a different substrate specificity of the repair activity encoded by the PSO1 and PSO3 genes.</description><subject>3-carboxypsoralen</subject><subject>Alleles</subject><subject>Biological and medical sciences</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>DNA Damage</subject><subject>DNA Repair</subject><subject>DNA, Fungal - genetics</subject><subject>DNA, Fungal - metabolism</subject><subject>epistasis</subject><subject>Epistasis, Genetic</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Furocoumarins - pharmacology</subject><subject>genes</subject><subject>Genes, Fungal</subject><subject>Genetics of eukaryotes. 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Psychology</topic><topic>Furocoumarins - pharmacology</topic><topic>genes</topic><topic>Genes, Fungal</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Human</topic><topic>methoxsalen</topic><topic>Methoxsalen - pharmacology</topic><topic>mutagenicity</topic><topic>mutants</topic><topic>Mutation</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae - radiation effects</topic><topic>ultraviolet radiation</topic><topic>Ultraviolet Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Benfato, M.S</creatorcontrib><creatorcontrib>Brendel, M</creatorcontrib><creatorcontrib>Henriques, J.A.P</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Benfato, M.S</au><au>Brendel, M</au><au>Henriques, J.A.P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA repair gene PSO3 of Saccharomyces cerevisiae belongs to the RAD3 epistasis group</atitle><jtitle>Current genetics</jtitle><addtitle>Curr Genet</addtitle><date>1992</date><risdate>1992</risdate><volume>21</volume><issue>1</issue><spage>85</spage><epage>90</epage><pages>85-90</pages><issn>0172-8083</issn><eissn>1432-0983</eissn><coden>CUGED5</coden><abstract>The mutant allele pso3-1 of Saccharomyces cerevisiae confers sensitivity to treatment with UV365nm (UVA) light-activated mono- and bi-functional psoralens. 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subjects 3-carboxypsoralen
Alleles
Biological and medical sciences
Classical genetics, quantitative genetics, hybrids
DNA Damage
DNA Repair
DNA, Fungal - genetics
DNA, Fungal - metabolism
epistasis
Epistasis, Genetic
Fundamental and applied biological sciences. Psychology
Furocoumarins - pharmacology
genes
Genes, Fungal
Genetics of eukaryotes. Biological and molecular evolution
Human
methoxsalen
Methoxsalen - pharmacology
mutagenicity
mutants
Mutation
Saccharomyces cerevisiae
Saccharomyces cerevisiae - genetics
Saccharomyces cerevisiae - metabolism
Saccharomyces cerevisiae - radiation effects
ultraviolet radiation
Ultraviolet Rays
title DNA repair gene PSO3 of Saccharomyces cerevisiae belongs to the RAD3 epistasis group
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