Formation of Large Palindromic DNA by Homologous Recombination of Short Inverted Repeat Sequences in Saccharomyces cerevisiae
Large DNA palindromes form sporadically in many eukaryotic and prokaryotic genomes and are often associated with amplified genes. The presence of a short inverted repeat sequence near a DNA double-strand break has been implicated in the formation of large palindromes in a variety of organisms. Previ...
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Veröffentlicht in: | Genetics (Austin) 2002-07, Vol.161 (3), p.1065-1075 |
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description | Large DNA palindromes form sporadically in many eukaryotic and prokaryotic genomes and are often associated with amplified genes. The presence of a short inverted repeat sequence near a DNA double-strand break has been implicated in the formation of large palindromes in a variety of organisms. Previously we have established that in Saccharomyces cerevisiae a linear DNA palindrome is efficiently formed from a single-copy circular plasmid when a DNA double-strand break is introduced next to a short inverted repeat sequence. In this study we address whether the linear palindromes form by an intermolecular reaction (that is, a reaction between two identical fragments in a head-to-head arrangement) or by an unusual intramolecular reaction, as it apparently does in other examples of palindrome formation. Our evidence supports a model in which palindromes are primarily formed by an intermolecular reaction involving homologous recombination of short inverted repeat sequences. We have also extended our investigation into the requirement for DNA double-strand break repair genes in palindrome formation. We have found that a deletion of the RAD52 gene significantly reduces palindrome formation by intermolecular recombination and that deletions of two other genes in the RAD52-epistasis group (RAD51 and MRE11) have little or no effect on palindrome formation. In addition, palindrome formation is dramatically reduced by a deletion of the nucleotide excision repair gene RAD1. |
doi_str_mv | 10.1093/genetics/161.3.1065 |
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The presence of a short inverted repeat sequence near a DNA double-strand break has been implicated in the formation of large palindromes in a variety of organisms. Previously we have established that in Saccharomyces cerevisiae a linear DNA palindrome is efficiently formed from a single-copy circular plasmid when a DNA double-strand break is introduced next to a short inverted repeat sequence. In this study we address whether the linear palindromes form by an intermolecular reaction (that is, a reaction between two identical fragments in a head-to-head arrangement) or by an unusual intramolecular reaction, as it apparently does in other examples of palindrome formation. Our evidence supports a model in which palindromes are primarily formed by an intermolecular reaction involving homologous recombination of short inverted repeat sequences. We have also extended our investigation into the requirement for DNA double-strand break repair genes in palindrome formation. We have found that a deletion of the RAD52 gene significantly reduces palindrome formation by intermolecular recombination and that deletions of two other genes in the RAD52-epistasis group (RAD51 and MRE11) have little or no effect on palindrome formation. In addition, palindrome formation is dramatically reduced by a deletion of the nucleotide excision repair gene RAD1.</description><identifier>ISSN: 0016-6731</identifier><identifier>ISSN: 1943-2631</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1093/genetics/161.3.1065</identifier><identifier>PMID: 12136011</identifier><identifier>CODEN: GENTAE</identifier><language>eng</language><publisher>United States: Genetics Soc America</publisher><subject>Base Sequence ; Deoxyribonucleic acid ; DNA ; DNA Damage ; DNA Repair - genetics ; DNA Repair Enzymes ; DNA, Fungal - genetics ; DNA-Binding Proteins ; Endonucleases - genetics ; Gene Amplification ; Genes ; Recombination, Genetic ; Repetitive Sequences, Nucleic Acid ; Restriction Mapping ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae Proteins</subject><ispartof>Genetics (Austin), 2002-07, Vol.161 (3), p.1065-1075</ispartof><rights>Copyright Genetics Society of America Jul 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c491t-7cb99206fb3463c501104727fbc3e99b7c0c480b40625294100f1e340e8487fd3</citedby><cites>FETCH-LOGICAL-c491t-7cb99206fb3463c501104727fbc3e99b7c0c480b40625294100f1e340e8487fd3</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/12136011$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Butler, David K</creatorcontrib><creatorcontrib>Gillespie, David</creatorcontrib><creatorcontrib>Steele, Brandi</creatorcontrib><title>Formation of Large Palindromic DNA by Homologous Recombination of Short Inverted Repeat Sequences in Saccharomyces cerevisiae</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>Large DNA palindromes form sporadically in many eukaryotic and prokaryotic genomes and are often associated with amplified genes. The presence of a short inverted repeat sequence near a DNA double-strand break has been implicated in the formation of large palindromes in a variety of organisms. Previously we have established that in Saccharomyces cerevisiae a linear DNA palindrome is efficiently formed from a single-copy circular plasmid when a DNA double-strand break is introduced next to a short inverted repeat sequence. In this study we address whether the linear palindromes form by an intermolecular reaction (that is, a reaction between two identical fragments in a head-to-head arrangement) or by an unusual intramolecular reaction, as it apparently does in other examples of palindrome formation. Our evidence supports a model in which palindromes are primarily formed by an intermolecular reaction involving homologous recombination of short inverted repeat sequences. We have also extended our investigation into the requirement for DNA double-strand break repair genes in palindrome formation. We have found that a deletion of the RAD52 gene significantly reduces palindrome formation by intermolecular recombination and that deletions of two other genes in the RAD52-epistasis group (RAD51 and MRE11) have little or no effect on palindrome formation. In addition, palindrome formation is dramatically reduced by a deletion of the nucleotide excision repair gene RAD1.</description><subject>Base Sequence</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Damage</subject><subject>DNA Repair - genetics</subject><subject>DNA Repair Enzymes</subject><subject>DNA, Fungal - genetics</subject><subject>DNA-Binding Proteins</subject><subject>Endonucleases - genetics</subject><subject>Gene Amplification</subject><subject>Genes</subject><subject>Recombination, Genetic</subject><subject>Repetitive Sequences, Nucleic Acid</subject><subject>Restriction Mapping</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae Proteins</subject><issn>0016-6731</issn><issn>1943-2631</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkVFv0zAUhSMEYt3gFyAhiwd4yuYbO078gjQNxiZVgCg8W457k3hK7M5OW_Vh_x1XLWPwZOne7xzd45Nlb4CeA5XsokOHkzXxAgScszQT5bNsBpKzvBAMnmczSkHkomJwkp3GeEcpFbKsX2YnUAATFGCWPVz7MOrJekd8S-Y6dEi-68G6ZfCjNeTT10vS7MiNH_3gO7-O5AcaPzbWPYoWvQ8TuXUbDBMu036FeiILvF-jMxiJdWShjel1ctztBwYDbmy0Gl9lL1o9RHx9fM-yX9eff17d5PNvX26vLue54RKmvDKNlAUVbcO4YKZMl1NeFVXbGIZSNpWhhte04VQUZSE5UNoCMk6x5nXVLtlZ9vHgu1o3Iy4NuinoQa2CHXXYKa-t-nfjbK86v1HARQFVnQzeHw2CT7nipEYbDQ6Ddpg-RUHNWQF8D777D7zz6-BSOJX2ALKiZYLYATLBxxiwfbwEqNp3q_50q1K3iql9t0n19mmIv5pjmQn4cAB62_VbG1DFUQ9DwkFtt9snVr8BvZuw4g</recordid><startdate>20020701</startdate><enddate>20020701</enddate><creator>Butler, David K</creator><creator>Gillespie, David</creator><creator>Steele, Brandi</creator><general>Genetics Soc America</general><general>Genetics Society of America</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>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>5PM</scope></search><sort><creationdate>20020701</creationdate><title>Formation of Large Palindromic DNA by Homologous Recombination of Short Inverted Repeat Sequences in Saccharomyces cerevisiae</title><author>Butler, David K ; Gillespie, David ; Steele, Brandi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c491t-7cb99206fb3463c501104727fbc3e99b7c0c480b40625294100f1e340e8487fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Base Sequence</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Damage</topic><topic>DNA Repair - genetics</topic><topic>DNA Repair Enzymes</topic><topic>DNA, Fungal - genetics</topic><topic>DNA-Binding Proteins</topic><topic>Endonucleases - genetics</topic><topic>Gene Amplification</topic><topic>Genes</topic><topic>Recombination, Genetic</topic><topic>Repetitive Sequences, Nucleic Acid</topic><topic>Restriction Mapping</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Butler, David K</creatorcontrib><creatorcontrib>Gillespie, David</creatorcontrib><creatorcontrib>Steele, Brandi</creatorcontrib><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 & 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 & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</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>Butler, David K</au><au>Gillespie, David</au><au>Steele, Brandi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Formation of Large Palindromic DNA by Homologous Recombination of Short Inverted Repeat Sequences in Saccharomyces cerevisiae</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>2002-07-01</date><risdate>2002</risdate><volume>161</volume><issue>3</issue><spage>1065</spage><epage>1075</epage><pages>1065-1075</pages><issn>0016-6731</issn><issn>1943-2631</issn><eissn>1943-2631</eissn><coden>GENTAE</coden><abstract>Large DNA palindromes form sporadically in many eukaryotic and prokaryotic genomes and are often associated with amplified genes. The presence of a short inverted repeat sequence near a DNA double-strand break has been implicated in the formation of large palindromes in a variety of organisms. Previously we have established that in Saccharomyces cerevisiae a linear DNA palindrome is efficiently formed from a single-copy circular plasmid when a DNA double-strand break is introduced next to a short inverted repeat sequence. In this study we address whether the linear palindromes form by an intermolecular reaction (that is, a reaction between two identical fragments in a head-to-head arrangement) or by an unusual intramolecular reaction, as it apparently does in other examples of palindrome formation. Our evidence supports a model in which palindromes are primarily formed by an intermolecular reaction involving homologous recombination of short inverted repeat sequences. We have also extended our investigation into the requirement for DNA double-strand break repair genes in palindrome formation. We have found that a deletion of the RAD52 gene significantly reduces palindrome formation by intermolecular recombination and that deletions of two other genes in the RAD52-epistasis group (RAD51 and MRE11) have little or no effect on palindrome formation. In addition, palindrome formation is dramatically reduced by a deletion of the nucleotide excision repair gene RAD1.</abstract><cop>United States</cop><pub>Genetics Soc America</pub><pmid>12136011</pmid><doi>10.1093/genetics/161.3.1065</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Base Sequence Deoxyribonucleic acid DNA DNA Damage DNA Repair - genetics DNA Repair Enzymes DNA, Fungal - genetics DNA-Binding Proteins Endonucleases - genetics Gene Amplification Genes Recombination, Genetic Repetitive Sequences, Nucleic Acid Restriction Mapping Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae Proteins |
title | Formation of Large Palindromic DNA by Homologous Recombination of Short Inverted Repeat Sequences in Saccharomyces cerevisiae |
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