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DNA with Different Local Torsional States Affects RecA‐Mediated Recombination Progression
DNA topology is thought to affect DNA enzyme activity. The helical structure of duplex DNA dictates the change of topological states during strand separation when DNA is constrained. During the repair of DNA double‐stranded breaks, the RecA nucleoprotein filament invades DNA and carries out consecut...
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Published in: | Chemphyschem 2017-03, Vol.18 (6), p.584-590 |
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description | DNA topology is thought to affect DNA enzyme activity. The helical structure of duplex DNA dictates the change of topological states during strand separation when DNA is constrained. During the repair of DNA double‐stranded breaks, the RecA nucleoprotein filament invades DNA and carries out consecutive strand exchange reactions coupled with duplex DNA strand separation. It has been suggested that torsional strain could be generated and its accumulation could inhibit strand exchange. We used hairpin and nicked DNA substrates to test how torsional strain alters the RecA‐mediated strand exchange efficiency. Single‐molecule tethered particle motion (TPM) experiments showed that torsionally constrained hairpin DNA substrates returned nearly no successful strand exchange events catalyzed by RecA. Surprisingly, the strand exchange efficiencies increase in the presence of DNA nicks or loop disruption. The dwell time of transient RecA events in hairpin is shorter compared to those found in nicked or fork DNA substrates, which suggests a limited strand exchange progression in hairpin substrates. Our observation shows that RecA generates local torsional strain during strand exchange, and the inability to dissipate this torsional strain inhibits homologous recombination progression. DNA topological states are thus important regulation measures of DNA recombination.
Single‐molecule tethered particle motion shows that RecA generates local torsional strain during strand exchange and inhibits homologous recombination progression. DNA topological states are important regulatory measures of DNA recombination. |
doi_str_mv | 10.1002/cphc.201601281 |
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Single‐molecule tethered particle motion shows that RecA generates local torsional strain during strand exchange and inhibits homologous recombination progression. DNA topological states are important regulatory measures of DNA recombination.</description><identifier>ISSN: 1439-4235</identifier><identifier>EISSN: 1439-7641</identifier><identifier>DOI: 10.1002/cphc.201601281</identifier><identifier>PMID: 28054431</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Deoxyribonucleic acid ; DNA ; DNA - chemistry ; DNA topology ; Rec A Recombinases - metabolism ; RecA-mediated strand exchange ; Recombination, Genetic ; single-molecule microscopy ; tethered particle motion ; torsional strain</subject><ispartof>Chemphyschem, 2017-03, Vol.18 (6), p.584-590</ispartof><rights>2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4431-16d962300296783b7cd12868c71c8a1e87eb888ca5b6b7ac38a7ea19b802e5af3</citedby><cites>FETCH-LOGICAL-c4431-16d962300296783b7cd12868c71c8a1e87eb888ca5b6b7ac38a7ea19b802e5af3</cites><orcidid>0000-0002-5614-3727</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28054431$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lu, Chih‐Hao</creatorcontrib><creatorcontrib>Li, Hung‐Wen</creatorcontrib><title>DNA with Different Local Torsional States Affects RecA‐Mediated Recombination Progression</title><title>Chemphyschem</title><addtitle>Chemphyschem</addtitle><description>DNA topology is thought to affect DNA enzyme activity. The helical structure of duplex DNA dictates the change of topological states during strand separation when DNA is constrained. During the repair of DNA double‐stranded breaks, the RecA nucleoprotein filament invades DNA and carries out consecutive strand exchange reactions coupled with duplex DNA strand separation. It has been suggested that torsional strain could be generated and its accumulation could inhibit strand exchange. We used hairpin and nicked DNA substrates to test how torsional strain alters the RecA‐mediated strand exchange efficiency. Single‐molecule tethered particle motion (TPM) experiments showed that torsionally constrained hairpin DNA substrates returned nearly no successful strand exchange events catalyzed by RecA. Surprisingly, the strand exchange efficiencies increase in the presence of DNA nicks or loop disruption. The dwell time of transient RecA events in hairpin is shorter compared to those found in nicked or fork DNA substrates, which suggests a limited strand exchange progression in hairpin substrates. Our observation shows that RecA generates local torsional strain during strand exchange, and the inability to dissipate this torsional strain inhibits homologous recombination progression. DNA topological states are thus important regulation measures of DNA recombination.
Single‐molecule tethered particle motion shows that RecA generates local torsional strain during strand exchange and inhibits homologous recombination progression. DNA topological states are important regulatory measures of DNA recombination.</description><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA - chemistry</subject><subject>DNA topology</subject><subject>Rec A Recombinases - metabolism</subject><subject>RecA-mediated strand exchange</subject><subject>Recombination, Genetic</subject><subject>single-molecule microscopy</subject><subject>tethered particle motion</subject><subject>torsional strain</subject><issn>1439-4235</issn><issn>1439-7641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkbFOwzAQhi0EolBYGVEkFpYW20lsZ6xaoEgFKigTQ-Q4F5oqqYudqOrGI_CMPAkOLUVigcln3_f_8t2P0AnBXYIxvVCLqepSTBgmVJAddEACP-pwFpDdTR1QP2yhQ2tnGGOBOdlHLSpwGAQ-OUDPg7uet8yrqTfIswwMzCtvpJUsvIk2NtdzVz1WsgLr9VxfVdZ7ANX7eHu_hTR372lz12WSz2XlcG9s9IsB20iP0F4mCwvHm7ONnq4uJ_1hZ3R_fdPvjTqq-UOHsDRi1HfTRIwLP-EqdbMwoThRQhIQHBIhhJJhwhIulS8kB0miRGAKocz8Njpf-y6Mfq3BVnGZWwVFIeegaxsTp464CIX4BxqGXEQUU4ee_UJnujZuH1-GGEeM-Q3VXVPKaGsNZPHC5KU0q5jguEkobhKKtwk5wenGtk5KSLf4dyQOiNbAMi9g9Ydd3B8P-z_mn6zenCs</recordid><startdate>20170317</startdate><enddate>20170317</enddate><creator>Lu, Chih‐Hao</creator><creator>Li, Hung‐Wen</creator><general>Wiley Subscription Services, Inc</general><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>K9.</scope><scope>7X8</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-5614-3727</orcidid></search><sort><creationdate>20170317</creationdate><title>DNA with Different Local Torsional States Affects RecA‐Mediated Recombination Progression</title><author>Lu, Chih‐Hao ; Li, Hung‐Wen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4431-16d962300296783b7cd12868c71c8a1e87eb888ca5b6b7ac38a7ea19b802e5af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA - chemistry</topic><topic>DNA topology</topic><topic>Rec A Recombinases - metabolism</topic><topic>RecA-mediated strand exchange</topic><topic>Recombination, Genetic</topic><topic>single-molecule microscopy</topic><topic>tethered particle motion</topic><topic>torsional strain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Chih‐Hao</creatorcontrib><creatorcontrib>Li, Hung‐Wen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Chemphyschem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Chih‐Hao</au><au>Li, Hung‐Wen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA with Different Local Torsional States Affects RecA‐Mediated Recombination Progression</atitle><jtitle>Chemphyschem</jtitle><addtitle>Chemphyschem</addtitle><date>2017-03-17</date><risdate>2017</risdate><volume>18</volume><issue>6</issue><spage>584</spage><epage>590</epage><pages>584-590</pages><issn>1439-4235</issn><eissn>1439-7641</eissn><abstract>DNA topology is thought to affect DNA enzyme activity. The helical structure of duplex DNA dictates the change of topological states during strand separation when DNA is constrained. During the repair of DNA double‐stranded breaks, the RecA nucleoprotein filament invades DNA and carries out consecutive strand exchange reactions coupled with duplex DNA strand separation. It has been suggested that torsional strain could be generated and its accumulation could inhibit strand exchange. We used hairpin and nicked DNA substrates to test how torsional strain alters the RecA‐mediated strand exchange efficiency. Single‐molecule tethered particle motion (TPM) experiments showed that torsionally constrained hairpin DNA substrates returned nearly no successful strand exchange events catalyzed by RecA. Surprisingly, the strand exchange efficiencies increase in the presence of DNA nicks or loop disruption. The dwell time of transient RecA events in hairpin is shorter compared to those found in nicked or fork DNA substrates, which suggests a limited strand exchange progression in hairpin substrates. Our observation shows that RecA generates local torsional strain during strand exchange, and the inability to dissipate this torsional strain inhibits homologous recombination progression. DNA topological states are thus important regulation measures of DNA recombination.
Single‐molecule tethered particle motion shows that RecA generates local torsional strain during strand exchange and inhibits homologous recombination progression. DNA topological states are important regulatory measures of DNA recombination.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28054431</pmid><doi>10.1002/cphc.201601281</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5614-3727</orcidid></addata></record> |
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subjects | Deoxyribonucleic acid DNA DNA - chemistry DNA topology Rec A Recombinases - metabolism RecA-mediated strand exchange Recombination, Genetic single-molecule microscopy tethered particle motion torsional strain |
title | DNA with Different Local Torsional States Affects RecA‐Mediated Recombination Progression |
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