Use of a cis‐acting mutation to study the role of FLP‐mediated recombination in the maintenance of native yeast 2μm plasmids
Summary The 2μm plasmid encodes a mechanism that ensures the partitioning of the plasmid at cell division. Little is known about the detailed mechanism of this partitioning system; for example, is there equal or unequal distribution of the plasmid molecules at mitosis? The plasmid also encodes a sit...
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Veröffentlicht in: | Molecular microbiology 1992-11, Vol.6 (21), p.3101-3107 |
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creator | Morrissey, Julie A. Cashmore, Annette M. |
description | Summary
The 2μm plasmid encodes a mechanism that ensures the partitioning of the plasmid at cell division. Little is known about the detailed mechanism of this partitioning system; for example, is there equal or unequal distribution of the plasmid molecules at mitosis? The plasmid also encodes a site‐specific recombination system that is thought to be involved in plasmid copy‐number amplification, although to date there has been no direct evidence that the recombination process itself is important for maintenance. We have identified a natural 2μm variant that has a cis‐acting mutation in the FLP‐mediated recombination system. We show that this plasmid is unable to amplify in vivo. Our results demonstrate that the average copy number per cell is not affected for the mutant but there is a large clonal variation. This is a direct demonstration that plasmid partitioning results in an unequal distribution of plasmids and that FLP‐mediated amplification compensates for this and therefore has an important role in maintenance. |
doi_str_mv | 10.1111/j.1365-2958.1992.tb01767.x |
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The 2μm plasmid encodes a mechanism that ensures the partitioning of the plasmid at cell division. Little is known about the detailed mechanism of this partitioning system; for example, is there equal or unequal distribution of the plasmid molecules at mitosis? The plasmid also encodes a site‐specific recombination system that is thought to be involved in plasmid copy‐number amplification, although to date there has been no direct evidence that the recombination process itself is important for maintenance. We have identified a natural 2μm variant that has a cis‐acting mutation in the FLP‐mediated recombination system. We show that this plasmid is unable to amplify in vivo. Our results demonstrate that the average copy number per cell is not affected for the mutant but there is a large clonal variation. This is a direct demonstration that plasmid partitioning results in an unequal distribution of plasmids and that FLP‐mediated amplification compensates for this and therefore has an important role in maintenance.</description><identifier>ISSN: 0950-382X</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1111/j.1365-2958.1992.tb01767.x</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Genic rearrangement. Recombination. Transposable element ; Molecular and cellular biology ; Molecular genetics ; Saccharomyces cerevisiae</subject><ispartof>Molecular microbiology, 1992-11, Vol.6 (21), p.3101-3107</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3771-251dc43a1926121eb1310763f3f6a7bf1d71401f9ff8112891fa30b530c094ae3</citedby><cites>FETCH-LOGICAL-c3771-251dc43a1926121eb1310763f3f6a7bf1d71401f9ff8112891fa30b530c094ae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2958.1992.tb01767.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2958.1992.tb01767.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4460396$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Morrissey, Julie A.</creatorcontrib><creatorcontrib>Cashmore, Annette M.</creatorcontrib><title>Use of a cis‐acting mutation to study the role of FLP‐mediated recombination in the maintenance of native yeast 2μm plasmids</title><title>Molecular microbiology</title><description>Summary
The 2μm plasmid encodes a mechanism that ensures the partitioning of the plasmid at cell division. Little is known about the detailed mechanism of this partitioning system; for example, is there equal or unequal distribution of the plasmid molecules at mitosis? The plasmid also encodes a site‐specific recombination system that is thought to be involved in plasmid copy‐number amplification, although to date there has been no direct evidence that the recombination process itself is important for maintenance. We have identified a natural 2μm variant that has a cis‐acting mutation in the FLP‐mediated recombination system. We show that this plasmid is unable to amplify in vivo. Our results demonstrate that the average copy number per cell is not affected for the mutant but there is a large clonal variation. This is a direct demonstration that plasmid partitioning results in an unequal distribution of plasmids and that FLP‐mediated amplification compensates for this and therefore has an important role in maintenance.</description><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genic rearrangement. Recombination. Transposable element</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Saccharomyces cerevisiae</subject><issn>0950-382X</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNqVkM9OGzEQhy1UJFLgHSxU9bZbj73rjXupKgQFKREcGqk3a9Zrg6P9k64dIDf6BjxQn6EP0SdhN4m4M5c5zPeb0XyEnAFLYagvyxSEzBOu8mkKSvE0lgwKWaRPB2TyNvpAJkzlLBFT_uuIfAxhyRgIJsWE_FkESztHkRof_j-_oIm-vaPNOmL0XUtjR0NcVxsa7y3tu3oLX85uB7SxlcdoK9pb0zWlb3cJ327ZBn0bbYut2UbG4YOlG4shUv7vb0NXNYbGV-GEHDqsgz3d92OyuLz4eX6VzG5-XJ9_nyVGFAUkPIfKZAJBcQkcbAkCWCGFE05iUTqoCsgYOOXcFIBPFTgUrMwFM0xlaMUx-bzbu-q732sbom58MLausbXdOmiQOc8yJQbw6w40fRdCb51e9b7BfqOB6dG6XupRrR7V6tG63lvXT0P40_4KBoO16wcBPrxtyDLJhJID9m2HPfrabt5xQM_n18PjIF4BHByaWQ</recordid><startdate>199211</startdate><enddate>199211</enddate><creator>Morrissey, Julie A.</creator><creator>Cashmore, Annette M.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>199211</creationdate><title>Use of a cis‐acting mutation to study the role of FLP‐mediated recombination in the maintenance of native yeast 2μm plasmids</title><author>Morrissey, Julie A. ; Cashmore, Annette M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3771-251dc43a1926121eb1310763f3f6a7bf1d71401f9ff8112891fa30b530c094ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genic rearrangement. Recombination. Transposable element</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Saccharomyces cerevisiae</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morrissey, Julie A.</creatorcontrib><creatorcontrib>Cashmore, Annette M.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</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 microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morrissey, Julie A.</au><au>Cashmore, Annette M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of a cis‐acting mutation to study the role of FLP‐mediated recombination in the maintenance of native yeast 2μm plasmids</atitle><jtitle>Molecular microbiology</jtitle><date>1992-11</date><risdate>1992</risdate><volume>6</volume><issue>21</issue><spage>3101</spage><epage>3107</epage><pages>3101-3107</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Summary
The 2μm plasmid encodes a mechanism that ensures the partitioning of the plasmid at cell division. Little is known about the detailed mechanism of this partitioning system; for example, is there equal or unequal distribution of the plasmid molecules at mitosis? The plasmid also encodes a site‐specific recombination system that is thought to be involved in plasmid copy‐number amplification, although to date there has been no direct evidence that the recombination process itself is important for maintenance. We have identified a natural 2μm variant that has a cis‐acting mutation in the FLP‐mediated recombination system. We show that this plasmid is unable to amplify in vivo. Our results demonstrate that the average copy number per cell is not affected for the mutant but there is a large clonal variation. This is a direct demonstration that plasmid partitioning results in an unequal distribution of plasmids and that FLP‐mediated amplification compensates for this and therefore has an important role in maintenance.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1111/j.1365-2958.1992.tb01767.x</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Fundamental and applied biological sciences. Psychology Genic rearrangement. Recombination. Transposable element Molecular and cellular biology Molecular genetics Saccharomyces cerevisiae |
title | Use of a cis‐acting mutation to study the role of FLP‐mediated recombination in the maintenance of native yeast 2μm plasmids |
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