Further characterization of the yeast pso4-1 mutant: interaction with rad51 and rad52 mutants after photoinduced psoralen lesions
The pso4-1 mutant was characterized as deficient in some types of recombination, including gene conversion, crossing over, and intrachromosomal recombination. The mode of interaction between pso4-1 and rad51 and between pso4-1 and rad52 mutants indicated that the PS04 gene belongs to the RAD52 epist...
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Veröffentlicht in: | Current genetics 1996-02, Vol.29 (3), p.211-218 |
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creator | Morais, M.A. de Jr Vicente, E.J Brozmanova, J Schenberg, A.C.G Henriques, J.A.P. (Universida de Federal de Rio Grande do Sul, Porto Alegre (Brazil). Dept. de Biofisica e Centro de Biotecnologia) |
description | The pso4-1 mutant was characterized as deficient in some types of recombination, including gene conversion, crossing over, and intrachromosomal recombination. The mode of interaction between pso4-1 and rad51 and between pso4-1 and rad52 mutants indicated that the PS04 gene belongs to the RAD52 epistasis group for strand-break repair. Moreover, the presence of the pso4-1 mutation decreased 8-MOP-photoinduced mutagenesis of the rad51 and rad52 mutants. Complementation tests using heterozygous diploid strains showed that the Pso4 protein might interact with the Rad52 protein during repair of 8-MOP photolesions. Thepso4-1 mutant, even though defective in inter- and intra-chromosomal recombination, conserves the ability for plasmid integration of circular and linear plasmid DNA. On the other hand, similar to the rad51 mutant, pso4-1 was able to incise but did not restore high-molecular-weight DNA during the repair of cross links induced by 8-MOP plus UVA. These results, together with those of previous reports, indicate that the PS04 gene belongs to the RAD52 DNA repair group and its product participates in the DNA rejoining step of the repair of cross-link lesions, which are crucial for induced mutagenesis and recombinogenesis. |
doi_str_mv | 10.1007/BF02221550 |
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(Universida de Federal de Rio Grande do Sul, Porto Alegre (Brazil). Dept. de Biofisica e Centro de Biotecnologia)</creator><creatorcontrib>Morais, M.A. de Jr ; Vicente, E.J ; Brozmanova, J ; Schenberg, A.C.G ; Henriques, J.A.P. (Universida de Federal de Rio Grande do Sul, Porto Alegre (Brazil). Dept. de Biofisica e Centro de Biotecnologia)</creatorcontrib><description>The pso4-1 mutant was characterized as deficient in some types of recombination, including gene conversion, crossing over, and intrachromosomal recombination. The mode of interaction between pso4-1 and rad51 and between pso4-1 and rad52 mutants indicated that the PS04 gene belongs to the RAD52 epistasis group for strand-break repair. Moreover, the presence of the pso4-1 mutation decreased 8-MOP-photoinduced mutagenesis of the rad51 and rad52 mutants. Complementation tests using heterozygous diploid strains showed that the Pso4 protein might interact with the Rad52 protein during repair of 8-MOP photolesions. Thepso4-1 mutant, even though defective in inter- and intra-chromosomal recombination, conserves the ability for plasmid integration of circular and linear plasmid DNA. On the other hand, similar to the rad51 mutant, pso4-1 was able to incise but did not restore high-molecular-weight DNA during the repair of cross links induced by 8-MOP plus UVA. These results, together with those of previous reports, indicate that the PS04 gene belongs to the RAD52 DNA repair group and its product participates in the DNA rejoining step of the repair of cross-link lesions, which are crucial for induced mutagenesis and recombinogenesis.</description><identifier>ISSN: 0172-8083</identifier><identifier>EISSN: 1432-0983</identifier><identifier>DOI: 10.1007/BF02221550</identifier><identifier>PMID: 8595666</identifier><language>eng</language><publisher>United States</publisher><subject>ADN ; DNA Repair - genetics ; DNA, Fungal - genetics ; DNA, Fungal - metabolism ; DNA-Binding Proteins - genetics ; Epistasis, Genetic ; Fungal Proteins - genetics ; Genes, Fungal ; Genetic Complementation Test ; INTERACCION DE GENES ; INTERACTION GENIQUE ; Methoxsalen - pharmacology ; MUTACION INDUCIDA ; Mutagenesis ; MUTANT ; MUTANTES ; Mutation ; MUTATION PROVOQUEE ; Plasmids ; Rad51 Recombinase ; Rad52 DNA Repair and Recombination Protein ; RECOMBINACION ; RECOMBINAISON ; Recombination, Genetic ; SACCHAROMYCES CEREVISIAE ; Saccharomyces cerevisiae - drug effects ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae Proteins ; Ultraviolet Rays</subject><ispartof>Current genetics, 1996-02, Vol.29 (3), p.211-218</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8595666$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morais, M.A. de Jr</creatorcontrib><creatorcontrib>Vicente, E.J</creatorcontrib><creatorcontrib>Brozmanova, J</creatorcontrib><creatorcontrib>Schenberg, A.C.G</creatorcontrib><creatorcontrib>Henriques, J.A.P. (Universida de Federal de Rio Grande do Sul, Porto Alegre (Brazil). Dept. de Biofisica e Centro de Biotecnologia)</creatorcontrib><title>Further characterization of the yeast pso4-1 mutant: interaction with rad51 and rad52 mutants after photoinduced psoralen lesions</title><title>Current genetics</title><addtitle>Curr Genet</addtitle><description>The pso4-1 mutant was characterized as deficient in some types of recombination, including gene conversion, crossing over, and intrachromosomal recombination. The mode of interaction between pso4-1 and rad51 and between pso4-1 and rad52 mutants indicated that the PS04 gene belongs to the RAD52 epistasis group for strand-break repair. Moreover, the presence of the pso4-1 mutation decreased 8-MOP-photoinduced mutagenesis of the rad51 and rad52 mutants. Complementation tests using heterozygous diploid strains showed that the Pso4 protein might interact with the Rad52 protein during repair of 8-MOP photolesions. Thepso4-1 mutant, even though defective in inter- and intra-chromosomal recombination, conserves the ability for plasmid integration of circular and linear plasmid DNA. On the other hand, similar to the rad51 mutant, pso4-1 was able to incise but did not restore high-molecular-weight DNA during the repair of cross links induced by 8-MOP plus UVA. These results, together with those of previous reports, indicate that the PS04 gene belongs to the RAD52 DNA repair group and its product participates in the DNA rejoining step of the repair of cross-link lesions, which are crucial for induced mutagenesis and recombinogenesis.</description><subject>ADN</subject><subject>DNA Repair - genetics</subject><subject>DNA, Fungal - genetics</subject><subject>DNA, Fungal - metabolism</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Epistasis, Genetic</subject><subject>Fungal Proteins - genetics</subject><subject>Genes, Fungal</subject><subject>Genetic Complementation Test</subject><subject>INTERACCION DE GENES</subject><subject>INTERACTION GENIQUE</subject><subject>Methoxsalen - pharmacology</subject><subject>MUTACION INDUCIDA</subject><subject>Mutagenesis</subject><subject>MUTANT</subject><subject>MUTANTES</subject><subject>Mutation</subject><subject>MUTATION PROVOQUEE</subject><subject>Plasmids</subject><subject>Rad51 Recombinase</subject><subject>Rad52 DNA Repair and Recombination Protein</subject><subject>RECOMBINACION</subject><subject>RECOMBINAISON</subject><subject>Recombination, Genetic</subject><subject>SACCHAROMYCES CEREVISIAE</subject><subject>Saccharomyces cerevisiae - drug effects</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>Ultraviolet Rays</subject><issn>0172-8083</issn><issn>1432-0983</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNot0D1PwzAQBmALgUopLIxISJ7YAv62w0ZLC0iVWGCOLolDgvKF7QiVjX9OSjPdSe9z73AIXVJySwnRd8sNYYxRKckRmlPBWURiw4_RnFDNIkMMP0Vn3n8SQpmJ9QzNjIylUmqOfjeDC6V1OCvBQRasq34gVF2LuwKPAd5Z8AH3vhMRxc0QoA33uGpHOOq9-65CiR3kkmJo8_-NTdBjKEaI-7ILXdXmQ2bzfZWD2ra4tn689-fopIDa24tpLtD7Zv22eo62r08vq4dtVDCpQpRLw5QRphC6IJynkAJYnQkljDIkZkYKnQqgVhmZKco5t0SmecpSI_JMEL5AN4fe3nVfg_UhaSqf2bqG1naDT6gmkknORng9wSFtbJ70rmrA7ZLpZ2N-dcgL6BL4cJVPHtexXiodC_4H-gp2OQ</recordid><startdate>19960201</startdate><enddate>19960201</enddate><creator>Morais, M.A. de Jr</creator><creator>Vicente, E.J</creator><creator>Brozmanova, J</creator><creator>Schenberg, A.C.G</creator><creator>Henriques, J.A.P. (Universida de Federal de Rio Grande do Sul, Porto Alegre (Brazil). Dept. de Biofisica e Centro de Biotecnologia)</creator><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19960201</creationdate><title>Further characterization of the yeast pso4-1 mutant: interaction with rad51 and rad52 mutants after photoinduced psoralen lesions</title><author>Morais, M.A. de Jr ; Vicente, E.J ; Brozmanova, J ; Schenberg, A.C.G ; Henriques, J.A.P. (Universida de Federal de Rio Grande do Sul, Porto Alegre (Brazil). Dept. de Biofisica e Centro de Biotecnologia)</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f256t-d5826848f47f033babaae7c4648680928547b4a1e685c61333e05bdb2b84dc403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>ADN</topic><topic>DNA Repair - genetics</topic><topic>DNA, Fungal - genetics</topic><topic>DNA, Fungal - metabolism</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Epistasis, Genetic</topic><topic>Fungal Proteins - genetics</topic><topic>Genes, Fungal</topic><topic>Genetic Complementation Test</topic><topic>INTERACCION DE GENES</topic><topic>INTERACTION GENIQUE</topic><topic>Methoxsalen - pharmacology</topic><topic>MUTACION INDUCIDA</topic><topic>Mutagenesis</topic><topic>MUTANT</topic><topic>MUTANTES</topic><topic>Mutation</topic><topic>MUTATION PROVOQUEE</topic><topic>Plasmids</topic><topic>Rad51 Recombinase</topic><topic>Rad52 DNA Repair and Recombination Protein</topic><topic>RECOMBINACION</topic><topic>RECOMBINAISON</topic><topic>Recombination, Genetic</topic><topic>SACCHAROMYCES CEREVISIAE</topic><topic>Saccharomyces cerevisiae - drug effects</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>Ultraviolet Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morais, M.A. de Jr</creatorcontrib><creatorcontrib>Vicente, E.J</creatorcontrib><creatorcontrib>Brozmanova, J</creatorcontrib><creatorcontrib>Schenberg, A.C.G</creatorcontrib><creatorcontrib>Henriques, J.A.P. (Universida de Federal de Rio Grande do Sul, Porto Alegre (Brazil). Dept. de Biofisica e Centro de Biotecnologia)</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Current genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morais, M.A. de Jr</au><au>Vicente, E.J</au><au>Brozmanova, J</au><au>Schenberg, A.C.G</au><au>Henriques, J.A.P. (Universida de Federal de Rio Grande do Sul, Porto Alegre (Brazil). Dept. de Biofisica e Centro de Biotecnologia)</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Further characterization of the yeast pso4-1 mutant: interaction with rad51 and rad52 mutants after photoinduced psoralen lesions</atitle><jtitle>Current genetics</jtitle><addtitle>Curr Genet</addtitle><date>1996-02-01</date><risdate>1996</risdate><volume>29</volume><issue>3</issue><spage>211</spage><epage>218</epage><pages>211-218</pages><issn>0172-8083</issn><eissn>1432-0983</eissn><abstract>The pso4-1 mutant was characterized as deficient in some types of recombination, including gene conversion, crossing over, and intrachromosomal recombination. The mode of interaction between pso4-1 and rad51 and between pso4-1 and rad52 mutants indicated that the PS04 gene belongs to the RAD52 epistasis group for strand-break repair. Moreover, the presence of the pso4-1 mutation decreased 8-MOP-photoinduced mutagenesis of the rad51 and rad52 mutants. Complementation tests using heterozygous diploid strains showed that the Pso4 protein might interact with the Rad52 protein during repair of 8-MOP photolesions. Thepso4-1 mutant, even though defective in inter- and intra-chromosomal recombination, conserves the ability for plasmid integration of circular and linear plasmid DNA. On the other hand, similar to the rad51 mutant, pso4-1 was able to incise but did not restore high-molecular-weight DNA during the repair of cross links induced by 8-MOP plus UVA. These results, together with those of previous reports, indicate that the PS04 gene belongs to the RAD52 DNA repair group and its product participates in the DNA rejoining step of the repair of cross-link lesions, which are crucial for induced mutagenesis and recombinogenesis.</abstract><cop>United States</cop><pmid>8595666</pmid><doi>10.1007/BF02221550</doi><tpages>8</tpages></addata></record> |
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subjects | ADN DNA Repair - genetics DNA, Fungal - genetics DNA, Fungal - metabolism DNA-Binding Proteins - genetics Epistasis, Genetic Fungal Proteins - genetics Genes, Fungal Genetic Complementation Test INTERACCION DE GENES INTERACTION GENIQUE Methoxsalen - pharmacology MUTACION INDUCIDA Mutagenesis MUTANT MUTANTES Mutation MUTATION PROVOQUEE Plasmids Rad51 Recombinase Rad52 DNA Repair and Recombination Protein RECOMBINACION RECOMBINAISON Recombination, Genetic SACCHAROMYCES CEREVISIAE Saccharomyces cerevisiae - drug effects Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae Proteins Ultraviolet Rays |
title | Further characterization of the yeast pso4-1 mutant: interaction with rad51 and rad52 mutants after photoinduced psoralen lesions |
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