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Bacterial DNA polymerases participate in oligonucleotide recombination
Summary Synthetic single‐strand oligonucleotides (oligos) with homology to genomic DNA have proved to be highly effective for constructing designed mutations in targeted genomes, a process referred to as recombineering. The cellular functions important for this type of homologous recombination have...
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Published in: | Molecular microbiology 2013-06, Vol.88 (5), p.906-920 |
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creator | Li, Xin‐tian Thomason, Lynn C. Sawitzke, James A. Costantino, Nina Court, Donald L. |
description | Summary
Synthetic single‐strand oligonucleotides (oligos) with homology to genomic DNA have proved to be highly effective for constructing designed mutations in targeted genomes, a process referred to as recombineering. The cellular functions important for this type of homologous recombination have yet to be determined. Towards this end, we have identified Escherichia coli functions that process the recombining oligo and affect bacteriophage λ Red‐mediated oligo recombination. To determine the nature of oligo processing during recombination, each oligo contained multiple nucleotide changes: a single base change allowing recombinant selection, and silent changes serving as genetic markers to determine the extent of oligo processing during the recombination. Such oligos were often not incorporated into the host chromosome intact; many were partially degraded in the process of recombination. The position and number of these silent nucleotide changes within the oligo strongly affect both oligo processing and recombination frequency. Exonucleases, especially those associated with DNA Polymerases I and III, affect inheritance of the silent nucleotide changes in the oligos. We demonstrate for the first time that the major DNA polymerases (Pol I and Pol III) and DNA ligase are directly involved with oligo recombination. |
doi_str_mv | 10.1111/mmi.12231 |
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Synthetic single‐strand oligonucleotides (oligos) with homology to genomic DNA have proved to be highly effective for constructing designed mutations in targeted genomes, a process referred to as recombineering. The cellular functions important for this type of homologous recombination have yet to be determined. Towards this end, we have identified Escherichia coli functions that process the recombining oligo and affect bacteriophage λ Red‐mediated oligo recombination. To determine the nature of oligo processing during recombination, each oligo contained multiple nucleotide changes: a single base change allowing recombinant selection, and silent changes serving as genetic markers to determine the extent of oligo processing during the recombination. Such oligos were often not incorporated into the host chromosome intact; many were partially degraded in the process of recombination. The position and number of these silent nucleotide changes within the oligo strongly affect both oligo processing and recombination frequency. Exonucleases, especially those associated with DNA Polymerases I and III, affect inheritance of the silent nucleotide changes in the oligos. We demonstrate for the first time that the major DNA polymerases (Pol I and Pol III) and DNA ligase are directly involved with oligo recombination.</description><identifier>ISSN: 0950-382X</identifier><identifier>ISSN: 1365-2958</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1111/mmi.12231</identifier><identifier>PMID: 23634873</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Bacteriophage lambda - genetics ; Chromosomes ; DNA Ligase ATP ; DNA Ligases - metabolism ; DNA polymerase ; DNA Polymerase I - metabolism ; DNA Polymerase III - metabolism ; DNA, Bacterial - metabolism ; E coli ; Escherichia coli ; Escherichia coli - enzymology ; Escherichia coli - genetics ; Genetic markers ; Genomics ; Oligonucleotides - metabolism ; Recombination, Genetic</subject><ispartof>Molecular microbiology, 2013-06, Vol.88 (5), p.906-920</ispartof><rights>Published 2013. This article is a U.S. Government work and is in the public domain in the USA</rights><rights>Published 2013. This article is a U.S. Government work and is in the public domain in the USA.</rights><rights>Copyright Blackwell Publishing Ltd. Jun 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4761-bfea955111488fa52a75fd5db6130e73b8ec3d3bb9dfd92470aab9e80f43275d3</citedby><cites>FETCH-LOGICAL-c4761-bfea955111488fa52a75fd5db6130e73b8ec3d3bb9dfd92470aab9e80f43275d3</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/23634873$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xin‐tian</creatorcontrib><creatorcontrib>Thomason, Lynn C.</creatorcontrib><creatorcontrib>Sawitzke, James A.</creatorcontrib><creatorcontrib>Costantino, Nina</creatorcontrib><creatorcontrib>Court, Donald L.</creatorcontrib><title>Bacterial DNA polymerases participate in oligonucleotide recombination</title><title>Molecular microbiology</title><addtitle>Mol Microbiol</addtitle><description>Summary
Synthetic single‐strand oligonucleotides (oligos) with homology to genomic DNA have proved to be highly effective for constructing designed mutations in targeted genomes, a process referred to as recombineering. The cellular functions important for this type of homologous recombination have yet to be determined. Towards this end, we have identified Escherichia coli functions that process the recombining oligo and affect bacteriophage λ Red‐mediated oligo recombination. To determine the nature of oligo processing during recombination, each oligo contained multiple nucleotide changes: a single base change allowing recombinant selection, and silent changes serving as genetic markers to determine the extent of oligo processing during the recombination. Such oligos were often not incorporated into the host chromosome intact; many were partially degraded in the process of recombination. The position and number of these silent nucleotide changes within the oligo strongly affect both oligo processing and recombination frequency. Exonucleases, especially those associated with DNA Polymerases I and III, affect inheritance of the silent nucleotide changes in the oligos. We demonstrate for the first time that the major DNA polymerases (Pol I and Pol III) and DNA ligase are directly involved with oligo recombination.</description><subject>Bacteriophage lambda - genetics</subject><subject>Chromosomes</subject><subject>DNA Ligase ATP</subject><subject>DNA Ligases - metabolism</subject><subject>DNA polymerase</subject><subject>DNA Polymerase I - metabolism</subject><subject>DNA Polymerase III - metabolism</subject><subject>DNA, Bacterial - metabolism</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Escherichia coli - enzymology</subject><subject>Escherichia coli - genetics</subject><subject>Genetic markers</subject><subject>Genomics</subject><subject>Oligonucleotides - metabolism</subject><subject>Recombination, Genetic</subject><issn>0950-382X</issn><issn>1365-2958</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkctKxTAURYMoen0M_AEpONFBNY-mbSaCbwUfEwVnIU1PNZI2NWmV-_dGr4oKgmeSwVks9slGaJ3gHRJnt23NDqGUkTk0ISznKRW8nEcTLDhOWUnvltByCI8YE4ZztoiWKMtZVhZsgk4OlB7AG2WTo6v9pHd22oJXAULSKz8YbXo1QGK6xFlz77pRW3CDqSHxoF1bmU4NxnWraKFRNsDax7uCbk-Obw7P0ovr0_PD_YtUZ0VO0qoBJTiPmbOybBSnquBNzesqj8mgYFUJmtWsqkTd1IJmBVaqElDiJmO04DVbQXszbz9WLdQausErK3tvWuWn0ikjf2468yDv3bMsOGU8y6Jg60Pg3dMIYZCtCRqsVR24MUjChBBYUP4flOfxGC7e0M1f6KMbfRd_IlJ5VpLoE5HanlHauxA8NF-5CZZvRcpYpHwvMrIb3w_9Ij-bi8DuDHgxFqZ_m-Tl5flM-Qqhvqg6</recordid><startdate>201306</startdate><enddate>201306</enddate><creator>Li, Xin‐tian</creator><creator>Thomason, Lynn C.</creator><creator>Sawitzke, James A.</creator><creator>Costantino, Nina</creator><creator>Court, Donald L.</creator><general>Blackwell Publishing Ltd</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7T7</scope><scope>5PM</scope></search><sort><creationdate>201306</creationdate><title>Bacterial DNA polymerases participate in oligonucleotide recombination</title><author>Li, Xin‐tian ; Thomason, Lynn C. ; Sawitzke, James A. ; Costantino, Nina ; Court, Donald L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4761-bfea955111488fa52a75fd5db6130e73b8ec3d3bb9dfd92470aab9e80f43275d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Bacteriophage lambda - genetics</topic><topic>Chromosomes</topic><topic>DNA Ligase ATP</topic><topic>DNA Ligases - metabolism</topic><topic>DNA polymerase</topic><topic>DNA Polymerase I - metabolism</topic><topic>DNA Polymerase III - metabolism</topic><topic>DNA, Bacterial - metabolism</topic><topic>E coli</topic><topic>Escherichia coli</topic><topic>Escherichia coli - enzymology</topic><topic>Escherichia coli - genetics</topic><topic>Genetic markers</topic><topic>Genomics</topic><topic>Oligonucleotides - metabolism</topic><topic>Recombination, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xin‐tian</creatorcontrib><creatorcontrib>Thomason, Lynn C.</creatorcontrib><creatorcontrib>Sawitzke, James A.</creatorcontrib><creatorcontrib>Costantino, Nina</creatorcontrib><creatorcontrib>Court, Donald L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</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>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xin‐tian</au><au>Thomason, Lynn C.</au><au>Sawitzke, James A.</au><au>Costantino, Nina</au><au>Court, Donald L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bacterial DNA polymerases participate in oligonucleotide recombination</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>2013-06</date><risdate>2013</risdate><volume>88</volume><issue>5</issue><spage>906</spage><epage>920</epage><pages>906-920</pages><issn>0950-382X</issn><issn>1365-2958</issn><eissn>1365-2958</eissn><abstract>Summary
Synthetic single‐strand oligonucleotides (oligos) with homology to genomic DNA have proved to be highly effective for constructing designed mutations in targeted genomes, a process referred to as recombineering. The cellular functions important for this type of homologous recombination have yet to be determined. Towards this end, we have identified Escherichia coli functions that process the recombining oligo and affect bacteriophage λ Red‐mediated oligo recombination. To determine the nature of oligo processing during recombination, each oligo contained multiple nucleotide changes: a single base change allowing recombinant selection, and silent changes serving as genetic markers to determine the extent of oligo processing during the recombination. Such oligos were often not incorporated into the host chromosome intact; many were partially degraded in the process of recombination. The position and number of these silent nucleotide changes within the oligo strongly affect both oligo processing and recombination frequency. Exonucleases, especially those associated with DNA Polymerases I and III, affect inheritance of the silent nucleotide changes in the oligos. We demonstrate for the first time that the major DNA polymerases (Pol I and Pol III) and DNA ligase are directly involved with oligo recombination.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23634873</pmid><doi>10.1111/mmi.12231</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteriophage lambda - genetics Chromosomes DNA Ligase ATP DNA Ligases - metabolism DNA polymerase DNA Polymerase I - metabolism DNA Polymerase III - metabolism DNA, Bacterial - metabolism E coli Escherichia coli Escherichia coli - enzymology Escherichia coli - genetics Genetic markers Genomics Oligonucleotides - metabolism Recombination, Genetic |
title | Bacterial DNA polymerases participate in oligonucleotide recombination |
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