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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Genetics (Austin) 1999-05, Vol.152 (1), p.117-128
Hauptverfasser: Jiao, K, Bullard, S.A, Salem, L, Malone, R.E
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 128
container_issue 1
container_start_page 117
container_title Genetics (Austin)
container_volume 152
creator Jiao, K
Bullard, S.A
Salem, L
Malone, R.E
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.
doi_str_mv 10.1093/genetics/152.1.117
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1460611</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>17222170</sourcerecordid><originalsourceid>FETCH-LOGICAL-c577t-c1e950a8ac6c72348e91f5b237f6c17bbdd80835e22e160dbda743420fbf1a0b3</originalsourceid><addsrcrecordid>eNqFkUFv1DAQhS0EokvhD3CAiAO3bGfsxE4uSGhFAakSh9Kz5TiTXVdJXOykq_57nG5bFi5cbGvmm6c3foy9RVgj1OJsSyNNzsYzLPka14jqGVthXYicS4HP2QoAZS6VwBP2KsZrAJB1Wb1kJwicF7xQKxY33ofWjWZyfsx8l007ytzoJvdUCWT90DwiZmzvmUDtbJeK6bPW3bq4NN2YDeR8dHF5Xhprdyb44c5SzCwFWjBDr9mLzvSR3jzcp-zq_MvPzbf84sfX75vPF7ktlZpyi1SXYCpjpVVcFBXV2JUNF6qTFlXTtG0FlSiJc0IJbdMaVYiCQ9d0aKARp-zTQfdmbgZqLY1TML2-CW4w4U574_TfndHt9NbfaiwkSMQk8PFBIPhfM8VJDy5a6nszkp-jlnXyJUX1XxAV5xwVJPDDP-C1n0P6w6g5FsgVliJB_ADZ4GMM1D1ZRtBL8voxeZ2S16hT8mno3fGyRyOHqP943Lntbu8C6TiYvk846v1-f6z0_gB2xmuzDS7qq0sOKIDX6RQgfgPcm8Vf</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>214127153</pqid></control><display><type>article</type><title>Coordination of the initiation of recombination and the reductional division in meiosis in Saccharomyces cerevisiae</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Jiao, K ; Bullard, S.A ; Salem, L ; Malone, R.E</creator><creatorcontrib>Jiao, K ; Bullard, S.A ; Salem, L ; Malone, R.E</creatorcontrib><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><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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0016-6731
ispartof Genetics (Austin), 1999-05, Vol.152 (1), p.117-128
issn 0016-6731
1943-2631
1943-2631
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1460611
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T01%3A38%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Coordination%20of%20the%20initiation%20of%20recombination%20and%20the%20reductional%20division%20in%20meiosis%20in%20Saccharomyces%20cerevisiae&rft.jtitle=Genetics%20(Austin)&rft.au=Jiao,%20K&rft.date=1999-05-01&rft.volume=152&rft.issue=1&rft.spage=117&rft.epage=128&rft.pages=117-128&rft.issn=0016-6731&rft.eissn=1943-2631&rft.coden=GENTAE&rft_id=info:doi/10.1093/genetics/152.1.117&rft_dat=%3Cproquest_pubme%3E17222170%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=214127153&rft_id=info:pmid/10224247&rfr_iscdi=true