Molecular Structures of Crossover and Noncrossover Intermediates during Gap Repair in Yeast: Implications for Recombination
The molecular structures of crossover (CO) and noncrossover (NCO) intermediates were determined by sequencing the products formed when a gapped plasmid was repaired using a diverged chromosomal template. Analyses were done in the absence of mismatch repair (MMR) to allow efficient detection of stran...
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Veröffentlicht in: | Molecular cell 2010-04, Vol.38 (2), p.211-222 |
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description | The molecular structures of crossover (CO) and noncrossover (NCO) intermediates were determined by sequencing the products formed when a gapped plasmid was repaired using a diverged chromosomal template. Analyses were done in the absence of mismatch repair (MMR) to allow efficient detection of strand-transfer intermediates, and the results reveal striking differences in the extents and locations of heteroduplex DNA (hDNA) in NCO versus CO products. These data indicate that most NCOs are produced by synthesis-dependent strand annealing rather than by a canonical double-strand break repair pathway and that resolution of Holliday junctions formed as part of the latter pathway is highly constrained to generate CO products. We suggest a model in which the length of hDNA formed by the initiating strand invasion event determines susceptibility of the resulting intermediate to antirecombination and ultimately whether a CO- or a NCO-producing pathway is followed.
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► Heteroduplex DNA position in gap-repair products reflects recombination mechanism ► Resolution of Holliday junctions is constrained to produce mostly crossover events ► Most noncrossovers are derived via a synthesis-dependent strand-annealing mechanism ► Mismatch-triggered antirecombination is separable from mismatch correction |
doi_str_mv | 10.1016/j.molcel.2010.02.028 |
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[Display omitted]
► Heteroduplex DNA position in gap-repair products reflects recombination mechanism ► Resolution of Holliday junctions is constrained to produce mostly crossover events ► Most noncrossovers are derived via a synthesis-dependent strand-annealing mechanism ► Mismatch-triggered antirecombination is separable from mismatch correction</description><identifier>ISSN: 1097-2765</identifier><identifier>EISSN: 1097-4164</identifier><identifier>DOI: 10.1016/j.molcel.2010.02.028</identifier><identifier>PMID: 20417600</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Chromosomes, Fungal - genetics ; Crossing Over, Genetic ; DNA ; DNA Repair - genetics ; DNA, Fungal - genetics ; Models, Genetic ; Nucleic Acid Heteroduplexes - genetics ; Nucleic Acid Heteroduplexes - metabolism ; Recombination, Genetic ; Saccharomyces cerevisiae - genetics</subject><ispartof>Molecular cell, 2010-04, Vol.38 (2), p.211-222</ispartof><rights>2010 Elsevier Inc.</rights><rights>Copyright 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c505t-4cbfaea0c6287fa22a24d09c7cc0caf85bc800f7be378d728e1aed2db14a46553</citedby><cites>FETCH-LOGICAL-c505t-4cbfaea0c6287fa22a24d09c7cc0caf85bc800f7be378d728e1aed2db14a46553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.molcel.2010.02.028$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20417600$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitchel, Katrina</creatorcontrib><creatorcontrib>Zhang, Hengshan</creatorcontrib><creatorcontrib>Welz-Voegele, Caroline</creatorcontrib><creatorcontrib>Jinks-Robertson, Sue</creatorcontrib><title>Molecular Structures of Crossover and Noncrossover Intermediates during Gap Repair in Yeast: Implications for Recombination</title><title>Molecular cell</title><addtitle>Mol Cell</addtitle><description>The molecular structures of crossover (CO) and noncrossover (NCO) intermediates were determined by sequencing the products formed when a gapped plasmid was repaired using a diverged chromosomal template. Analyses were done in the absence of mismatch repair (MMR) to allow efficient detection of strand-transfer intermediates, and the results reveal striking differences in the extents and locations of heteroduplex DNA (hDNA) in NCO versus CO products. These data indicate that most NCOs are produced by synthesis-dependent strand annealing rather than by a canonical double-strand break repair pathway and that resolution of Holliday junctions formed as part of the latter pathway is highly constrained to generate CO products. We suggest a model in which the length of hDNA formed by the initiating strand invasion event determines susceptibility of the resulting intermediate to antirecombination and ultimately whether a CO- or a NCO-producing pathway is followed.
[Display omitted]
► Heteroduplex DNA position in gap-repair products reflects recombination mechanism ► Resolution of Holliday junctions is constrained to produce mostly crossover events ► Most noncrossovers are derived via a synthesis-dependent strand-annealing mechanism ► Mismatch-triggered antirecombination is separable from mismatch correction</description><subject>Chromosomes, Fungal - genetics</subject><subject>Crossing Over, Genetic</subject><subject>DNA</subject><subject>DNA Repair - genetics</subject><subject>DNA, Fungal - genetics</subject><subject>Models, Genetic</subject><subject>Nucleic Acid Heteroduplexes - genetics</subject><subject>Nucleic Acid Heteroduplexes - metabolism</subject><subject>Recombination, Genetic</subject><subject>Saccharomyces cerevisiae - genetics</subject><issn>1097-2765</issn><issn>1097-4164</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkdFrFDEQxkNR2tr2PyiSN5_unGSzm6wPghy1HlSFtj74FLLZWcmxm6xJtiD-86a9s48KAzN8_GYGvo-QSwZrBqx5u1tPYbQ4rjkUCXgpdUROGbRyJVgjXhxmLpv6hLxKaQfARK3aY3LCQTDZAJyS35_DiHYZTaR3OS42LxETDQPdxJBSeMBIje_pl-Dts7D1GeOEvTO5sP0Snf9Br81Mb3E2LlLn6Xc0Kb-j22kenTXZBZ_oEGIhbJg655-kc_JyMGPCi0M_I98-Xt1vPq1uvl5vNx9uVraGOq-E7QaDBmzDlRwM54aLHlorrQVrBlV3VgEMssNKql5yhcxgz_uOCSOauq7OyJv93TmGnwumrCeXinOj8RiWpFXbsoZVDf8vKauqZVU5WUixJ59siTjoObrJxF-agX7MR-_0Ph_9mI8GXkqVtdeHB0tXHHxe-htIAd7vASyGPDiMOlmH3ha3I9qs--D-_eEPsuCmDw</recordid><startdate>20100423</startdate><enddate>20100423</enddate><creator>Mitchel, Katrina</creator><creator>Zhang, Hengshan</creator><creator>Welz-Voegele, Caroline</creator><creator>Jinks-Robertson, Sue</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20100423</creationdate><title>Molecular Structures of Crossover and Noncrossover Intermediates during Gap Repair in Yeast: Implications for Recombination</title><author>Mitchel, Katrina ; Zhang, Hengshan ; Welz-Voegele, Caroline ; Jinks-Robertson, Sue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-4cbfaea0c6287fa22a24d09c7cc0caf85bc800f7be378d728e1aed2db14a46553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Chromosomes, Fungal - genetics</topic><topic>Crossing Over, Genetic</topic><topic>DNA</topic><topic>DNA Repair - genetics</topic><topic>DNA, Fungal - genetics</topic><topic>Models, Genetic</topic><topic>Nucleic Acid Heteroduplexes - genetics</topic><topic>Nucleic Acid Heteroduplexes - metabolism</topic><topic>Recombination, Genetic</topic><topic>Saccharomyces cerevisiae - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitchel, Katrina</creatorcontrib><creatorcontrib>Zhang, Hengshan</creatorcontrib><creatorcontrib>Welz-Voegele, Caroline</creatorcontrib><creatorcontrib>Jinks-Robertson, Sue</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><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>Molecular cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitchel, Katrina</au><au>Zhang, Hengshan</au><au>Welz-Voegele, Caroline</au><au>Jinks-Robertson, Sue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Structures of Crossover and Noncrossover Intermediates during Gap Repair in Yeast: Implications for Recombination</atitle><jtitle>Molecular cell</jtitle><addtitle>Mol Cell</addtitle><date>2010-04-23</date><risdate>2010</risdate><volume>38</volume><issue>2</issue><spage>211</spage><epage>222</epage><pages>211-222</pages><issn>1097-2765</issn><eissn>1097-4164</eissn><abstract>The molecular structures of crossover (CO) and noncrossover (NCO) intermediates were determined by sequencing the products formed when a gapped plasmid was repaired using a diverged chromosomal template. Analyses were done in the absence of mismatch repair (MMR) to allow efficient detection of strand-transfer intermediates, and the results reveal striking differences in the extents and locations of heteroduplex DNA (hDNA) in NCO versus CO products. These data indicate that most NCOs are produced by synthesis-dependent strand annealing rather than by a canonical double-strand break repair pathway and that resolution of Holliday junctions formed as part of the latter pathway is highly constrained to generate CO products. We suggest a model in which the length of hDNA formed by the initiating strand invasion event determines susceptibility of the resulting intermediate to antirecombination and ultimately whether a CO- or a NCO-producing pathway is followed.
[Display omitted]
► Heteroduplex DNA position in gap-repair products reflects recombination mechanism ► Resolution of Holliday junctions is constrained to produce mostly crossover events ► Most noncrossovers are derived via a synthesis-dependent strand-annealing mechanism ► Mismatch-triggered antirecombination is separable from mismatch correction</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20417600</pmid><doi>10.1016/j.molcel.2010.02.028</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Chromosomes, Fungal - genetics Crossing Over, Genetic DNA DNA Repair - genetics DNA, Fungal - genetics Models, Genetic Nucleic Acid Heteroduplexes - genetics Nucleic Acid Heteroduplexes - metabolism Recombination, Genetic Saccharomyces cerevisiae - genetics |
title | Molecular Structures of Crossover and Noncrossover Intermediates during Gap Repair in Yeast: Implications for Recombination |
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