Coordination of the initiation of recombination and the reductional division in meiosis in Saccharomyces cerevisiae
Early exchange (EE) genes are required for the initiation of meiotic recombination in Saccharomyces cerevisiae. Cells with mutations in several EE genes undergo an earlier reductional division (MI), which suggests that the initiation of meiotic recombination is involved in determining proper timing...
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Veröffentlicht in: | Genetics (Austin) 1999-05, Vol.152 (1), p.117-128 |
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description | Early exchange (EE) genes are required for the initiation of meiotic recombination in Saccharomyces cerevisiae. Cells with mutations in several EE genes undergo an earlier reductional division (MI), which suggests that the initiation of meiotic recombination is involved in determining proper timing of the division. The different effects of null mutations on the timing of reductional division allow EE genes to be assorted into three classes: mutations in RAD50 or REC102 that confer a very early reductional division; mutations in REC104 or REC114 that confer a division earlier than that of wild-type (WT) cells, but later than that of mutants of the first class; and mutations in MEI4 that do not significantly alter the timing of MI. The very early mutations are epistatic to mutations in the other two classes. We propose a model that accounts for the epistatic relationships and the communication between recombination initiation and the first division. Data in this article indicate that double-strand breaks (DSBs) are not the signal for the normal delay of reductional division; these experiments also confirm that MEI4 is required for the formation of meiotic DSBs. Finally, if a DSB is provided by the HO endonuclease, recombination can occur in the absence of MEI4 and REC104. |
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Cells with mutations in several EE genes undergo an earlier reductional division (MI), which suggests that the initiation of meiotic recombination is involved in determining proper timing of the division. The different effects of null mutations on the timing of reductional division allow EE genes to be assorted into three classes: mutations in RAD50 or REC102 that confer a very early reductional division; mutations in REC104 or REC114 that confer a division earlier than that of wild-type (WT) cells, but later than that of mutants of the first class; and mutations in MEI4 that do not significantly alter the timing of MI. The very early mutations are epistatic to mutations in the other two classes. We propose a model that accounts for the epistatic relationships and the communication between recombination initiation and the first division. Data in this article indicate that double-strand breaks (DSBs) are not the signal for the normal delay of reductional division; these experiments also confirm that MEI4 is required for the formation of meiotic DSBs. Finally, if a DSB is provided by the HO endonuclease, recombination can occur in the absence of MEI4 and REC104.</description><identifier>ISSN: 0016-6731</identifier><identifier>ISSN: 1943-2631</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1093/genetics/152.1.117</identifier><identifier>PMID: 10224247</identifier><identifier>CODEN: GENTAE</identifier><language>eng</language><publisher>United States: Genetics Soc America</publisher><subject>Blotting, Southern ; Cells ; Deoxyribonucleases, Type II Site-Specific - genetics ; Deoxyribonucleic acid ; DNA ; DNA Damage ; dna double strand breaks ; dna modification ; DNA-Binding Proteins ; epistasis ; Epistasis, Genetic ; Fungal Proteins - genetics ; Genes ; genetic recombination ; Genotype ; ho nuclease ; Indoles - metabolism ; initiation ; loci ; mat locus ; Meiosis ; Models, Genetic ; mutants ; Mutation ; Nuclear Proteins ; nucleases ; phenotype ; Plasmids ; Recombinases ; Recombination, Genetic ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae Proteins ; sporulation ; Time Factors</subject><ispartof>Genetics (Austin), 1999-05, Vol.152 (1), p.117-128</ispartof><rights>Copyright Genetics Society of America May 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c577t-c1e950a8ac6c72348e91f5b237f6c17bbdd80835e22e160dbda743420fbf1a0b3</citedby><cites>FETCH-LOGICAL-c577t-c1e950a8ac6c72348e91f5b237f6c17bbdd80835e22e160dbda743420fbf1a0b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10224247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiao, K</creatorcontrib><creatorcontrib>Bullard, S.A</creatorcontrib><creatorcontrib>Salem, L</creatorcontrib><creatorcontrib>Malone, R.E</creatorcontrib><title>Coordination of the initiation of recombination and the reductional division in meiosis in Saccharomyces cerevisiae</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>Early exchange (EE) genes are required for the initiation of meiotic recombination in Saccharomyces cerevisiae. Cells with mutations in several EE genes undergo an earlier reductional division (MI), which suggests that the initiation of meiotic recombination is involved in determining proper timing of the division. The different effects of null mutations on the timing of reductional division allow EE genes to be assorted into three classes: mutations in RAD50 or REC102 that confer a very early reductional division; mutations in REC104 or REC114 that confer a division earlier than that of wild-type (WT) cells, but later than that of mutants of the first class; and mutations in MEI4 that do not significantly alter the timing of MI. The very early mutations are epistatic to mutations in the other two classes. We propose a model that accounts for the epistatic relationships and the communication between recombination initiation and the first division. Data in this article indicate that double-strand breaks (DSBs) are not the signal for the normal delay of reductional division; these experiments also confirm that MEI4 is required for the formation of meiotic DSBs. Finally, if a DSB is provided by the HO endonuclease, recombination can occur in the absence of MEI4 and REC104.</description><subject>Blotting, Southern</subject><subject>Cells</subject><subject>Deoxyribonucleases, Type II Site-Specific - genetics</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Damage</subject><subject>dna double strand breaks</subject><subject>dna modification</subject><subject>DNA-Binding Proteins</subject><subject>epistasis</subject><subject>Epistasis, Genetic</subject><subject>Fungal Proteins - genetics</subject><subject>Genes</subject><subject>genetic recombination</subject><subject>Genotype</subject><subject>ho nuclease</subject><subject>Indoles - metabolism</subject><subject>initiation</subject><subject>loci</subject><subject>mat locus</subject><subject>Meiosis</subject><subject>Models, Genetic</subject><subject>mutants</subject><subject>Mutation</subject><subject>Nuclear Proteins</subject><subject>nucleases</subject><subject>phenotype</subject><subject>Plasmids</subject><subject>Recombinases</subject><subject>Recombination, Genetic</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>sporulation</subject><subject>Time Factors</subject><issn>0016-6731</issn><issn>1943-2631</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EokvhD3CAiAO3bGfsxE4uSGhFAakSh9Kz5TiTXVdJXOykq_57nG5bFi5cbGvmm6c3foy9RVgj1OJsSyNNzsYzLPka14jqGVthXYicS4HP2QoAZS6VwBP2KsZrAJB1Wb1kJwicF7xQKxY33ofWjWZyfsx8l007ytzoJvdUCWT90DwiZmzvmUDtbJeK6bPW3bq4NN2YDeR8dHF5Xhprdyb44c5SzCwFWjBDr9mLzvSR3jzcp-zq_MvPzbf84sfX75vPF7ktlZpyi1SXYCpjpVVcFBXV2JUNF6qTFlXTtG0FlSiJc0IJbdMaVYiCQ9d0aKARp-zTQfdmbgZqLY1TML2-CW4w4U574_TfndHt9NbfaiwkSMQk8PFBIPhfM8VJDy5a6nszkp-jlnXyJUX1XxAV5xwVJPDDP-C1n0P6w6g5FsgVliJB_ADZ4GMM1D1ZRtBL8voxeZ2S16hT8mno3fGyRyOHqP943Lntbu8C6TiYvk846v1-f6z0_gB2xmuzDS7qq0sOKIDX6RQgfgPcm8Vf</recordid><startdate>19990501</startdate><enddate>19990501</enddate><creator>Jiao, K</creator><creator>Bullard, S.A</creator><creator>Salem, L</creator><creator>Malone, R.E</creator><general>Genetics Soc America</general><general>Genetics Society of America</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>4U-</scope><scope>7QP</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19990501</creationdate><title>Coordination of the initiation of recombination and the reductional division in meiosis in Saccharomyces cerevisiae</title><author>Jiao, K ; Bullard, S.A ; Salem, L ; Malone, R.E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c577t-c1e950a8ac6c72348e91f5b237f6c17bbdd80835e22e160dbda743420fbf1a0b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Blotting, Southern</topic><topic>Cells</topic><topic>Deoxyribonucleases, Type II Site-Specific - genetics</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Damage</topic><topic>dna double strand breaks</topic><topic>dna modification</topic><topic>DNA-Binding Proteins</topic><topic>epistasis</topic><topic>Epistasis, Genetic</topic><topic>Fungal Proteins - genetics</topic><topic>Genes</topic><topic>genetic recombination</topic><topic>Genotype</topic><topic>ho nuclease</topic><topic>Indoles - metabolism</topic><topic>initiation</topic><topic>loci</topic><topic>mat locus</topic><topic>Meiosis</topic><topic>Models, Genetic</topic><topic>mutants</topic><topic>Mutation</topic><topic>Nuclear Proteins</topic><topic>nucleases</topic><topic>phenotype</topic><topic>Plasmids</topic><topic>Recombinases</topic><topic>Recombination, Genetic</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>sporulation</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiao, K</creatorcontrib><creatorcontrib>Bullard, S.A</creatorcontrib><creatorcontrib>Salem, L</creatorcontrib><creatorcontrib>Malone, R.E</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genetics (Austin)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiao, K</au><au>Bullard, S.A</au><au>Salem, L</au><au>Malone, R.E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coordination of the initiation of recombination and the reductional division in meiosis in Saccharomyces cerevisiae</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>1999-05-01</date><risdate>1999</risdate><volume>152</volume><issue>1</issue><spage>117</spage><epage>128</epage><pages>117-128</pages><issn>0016-6731</issn><issn>1943-2631</issn><eissn>1943-2631</eissn><coden>GENTAE</coden><abstract>Early exchange (EE) genes are required for the initiation of meiotic recombination in Saccharomyces cerevisiae. Cells with mutations in several EE genes undergo an earlier reductional division (MI), which suggests that the initiation of meiotic recombination is involved in determining proper timing of the division. The different effects of null mutations on the timing of reductional division allow EE genes to be assorted into three classes: mutations in RAD50 or REC102 that confer a very early reductional division; mutations in REC104 or REC114 that confer a division earlier than that of wild-type (WT) cells, but later than that of mutants of the first class; and mutations in MEI4 that do not significantly alter the timing of MI. The very early mutations are epistatic to mutations in the other two classes. We propose a model that accounts for the epistatic relationships and the communication between recombination initiation and the first division. Data in this article indicate that double-strand breaks (DSBs) are not the signal for the normal delay of reductional division; these experiments also confirm that MEI4 is required for the formation of meiotic DSBs. Finally, if a DSB is provided by the HO endonuclease, recombination can occur in the absence of MEI4 and REC104.</abstract><cop>United States</cop><pub>Genetics Soc America</pub><pmid>10224247</pmid><doi>10.1093/genetics/152.1.117</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Blotting, Southern Cells Deoxyribonucleases, Type II Site-Specific - genetics Deoxyribonucleic acid DNA DNA Damage dna double strand breaks dna modification DNA-Binding Proteins epistasis Epistasis, Genetic Fungal Proteins - genetics Genes genetic recombination Genotype ho nuclease Indoles - metabolism initiation loci mat locus Meiosis Models, Genetic mutants Mutation Nuclear Proteins nucleases phenotype Plasmids Recombinases Recombination, Genetic Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae Proteins sporulation Time Factors |
title | Coordination of the initiation of recombination and the reductional division in meiosis in Saccharomyces cerevisiae |
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