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Repair of single- and multiple-substitution mismatches during recombination in Streptococcus pneumoniae
The use as genetic markers, during transformation of Streptococcus pneumoniae, of 19 sequences differing from wild type, located throughout the amiA locus, enabled us to examine the fate of 24 single- and 11 multiple-mismatches during recombination. Tentative mismatch ranking as a function of decrea...
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Published in: | Genetics (Austin) 1989, Vol.121 (1), p.29-36 |
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description | The use as genetic markers, during transformation of Streptococcus pneumoniae, of 19 sequences differing from wild type, located throughout the amiA locus, enabled us to examine the fate of 24 single- and 11 multiple-mismatches during recombination. Tentative mismatch ranking as a function of decreasing repair efficiency by the Hex mismatch repair system is G/T = A/C = G/G (maximum repair: 90-95%) greater than C/T (mostly 75 to 90% repair) greater than A/A (from 50 to 90% repair) greater than T/T (50-65% repair) greater than A/G (from 0 to 20% repair) greater than C/C. No indication of correction of the latter has been obtained. Over the limited number of samples examined, we observed no influence of the base composition of the surrounding sequence on correction efficiency for both transition mismatches and for G/G and C/C. Variations in the surrounding sequence affect repair of A/G and C/T, and, even more strongly, of A/A and T/T. No simple correlation to the G:C content of the surrounding sequence is apparent from our results, in contrast to the conclusion drawn for the Mut mismatch repair system of Escherichia coli. Examination of the fate of multiple mismatches suggests that C/C may sometimes impede recognition of otherwise corrected mismatches. |
doi_str_mv | 10.1093/genetics/121.1.29 |
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Tentative mismatch ranking as a function of decreasing repair efficiency by the Hex mismatch repair system is G/T = A/C = G/G (maximum repair: 90-95%) greater than C/T (mostly 75 to 90% repair) greater than A/A (from 50 to 90% repair) greater than T/T (50-65% repair) greater than A/G (from 0 to 20% repair) greater than C/C. No indication of correction of the latter has been obtained. Over the limited number of samples examined, we observed no influence of the base composition of the surrounding sequence on correction efficiency for both transition mismatches and for G/G and C/C. Variations in the surrounding sequence affect repair of A/G and C/T, and, even more strongly, of A/A and T/T. No simple correlation to the G:C content of the surrounding sequence is apparent from our results, in contrast to the conclusion drawn for the Mut mismatch repair system of Escherichia coli. Examination of the fate of multiple mismatches suggests that C/C may sometimes impede recognition of otherwise corrected mismatches.</description><identifier>ISSN: 0016-6731</identifier><identifier>ISSN: 1943-2631</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1093/genetics/121.1.29</identifier><identifier>PMID: 2645195</identifier><identifier>CODEN: GENTAE</identifier><language>eng</language><publisher>Bethesda, MD: Genetics Society of America</publisher><subject>Base Composition ; Biological and medical sciences ; DNA Repair ; DNA, Bacterial - genetics ; Escherichia coli - genetics ; Fundamental and applied biological sciences. Psychology ; Genetic Markers ; Investigations ; Molecular and cellular biology ; Molecular genetics ; Mutagenesis. Repair ; Recombination, Genetic ; Streptococcus pneumoniae ; Streptococcus pneumoniae - genetics ; Transformation, Bacterial</subject><ispartof>Genetics (Austin), 1989, Vol.121 (1), p.29-36</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3699-cba25b68f7f671f8541d265f3b883fcc652eacda0f29836678b628ba98ed091d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7214212$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2645195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GASC, A.-M</creatorcontrib><creatorcontrib>SICARD, A.-M</creatorcontrib><creatorcontrib>CLAVERYS, J.-P</creatorcontrib><title>Repair of single- and multiple-substitution mismatches during recombination in Streptococcus pneumoniae</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>The use as genetic markers, during transformation of Streptococcus pneumoniae, of 19 sequences differing from wild type, located throughout the amiA locus, enabled us to examine the fate of 24 single- and 11 multiple-mismatches during recombination. Tentative mismatch ranking as a function of decreasing repair efficiency by the Hex mismatch repair system is G/T = A/C = G/G (maximum repair: 90-95%) greater than C/T (mostly 75 to 90% repair) greater than A/A (from 50 to 90% repair) greater than T/T (50-65% repair) greater than A/G (from 0 to 20% repair) greater than C/C. No indication of correction of the latter has been obtained. Over the limited number of samples examined, we observed no influence of the base composition of the surrounding sequence on correction efficiency for both transition mismatches and for G/G and C/C. Variations in the surrounding sequence affect repair of A/G and C/T, and, even more strongly, of A/A and T/T. No simple correlation to the G:C content of the surrounding sequence is apparent from our results, in contrast to the conclusion drawn for the Mut mismatch repair system of Escherichia coli. Examination of the fate of multiple mismatches suggests that C/C may sometimes impede recognition of otherwise corrected mismatches.</description><subject>Base Composition</subject><subject>Biological and medical sciences</subject><subject>DNA Repair</subject><subject>DNA, Bacterial - genetics</subject><subject>Escherichia coli - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Markers</subject><subject>Investigations</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Mutagenesis. Repair</subject><subject>Recombination, Genetic</subject><subject>Streptococcus pneumoniae</subject><subject>Streptococcus pneumoniae - genetics</subject><subject>Transformation, Bacterial</subject><issn>0016-6731</issn><issn>1943-2631</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNqFkUuLFTEQhYMo43X0B7gQshB3fSeVdKeTjSCDLxgQnHEd0unkTqQ7afMQ_PcTnetFV7MqivPVqSoOQi-B7IFIdnGwwRZv8gVQ2MOeykdoB7JnHeUMHqMdIcA7PjJ4ip7l_J0QwuUgztAZ5f0Actihw1e7aZ9wdDj7cFhsh3WY8VqX4rfW5Trl4kstPga8-rzqYm5txnNNDcfJmrhOPug_ug_4uiS7lWiiMTXjLdi6xuC1fY6eOL1k--JYz9G3D-9vLj91V18-fr58d9UZxqXszKTpMHHhRsdHcGLoYaZ8cGwSgjlj-ECtNrMmjkrBOB_FxKmYtBR2JhJmdo7e3vtudVrtbGwoSS9qS37V6ZeK2qv_leBv1SH-VEAJ44Q2gzdHgxR_VJuLal8buyw62FizGoXgsm1-EISBjT2lYwPhHjQp5pysO10DRP2OUf2NsR0BChSVbebVv2-cJo65Nf31UdfZ6MUlHYzPJ2yk0FOg7A6veatr</recordid><startdate>1989</startdate><enddate>1989</enddate><creator>GASC, A.-M</creator><creator>SICARD, A.-M</creator><creator>CLAVERYS, J.-P</creator><general>Genetics Society of America</general><scope>IQODW</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>7QL</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>1989</creationdate><title>Repair of single- and multiple-substitution mismatches during recombination in Streptococcus pneumoniae</title><author>GASC, A.-M ; SICARD, A.-M ; CLAVERYS, J.-P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3699-cba25b68f7f671f8541d265f3b883fcc652eacda0f29836678b628ba98ed091d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Base Composition</topic><topic>Biological and medical sciences</topic><topic>DNA Repair</topic><topic>DNA, Bacterial - genetics</topic><topic>Escherichia coli - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Markers</topic><topic>Investigations</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Mutagenesis. Repair</topic><topic>Recombination, Genetic</topic><topic>Streptococcus pneumoniae</topic><topic>Streptococcus pneumoniae - genetics</topic><topic>Transformation, Bacterial</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GASC, A.-M</creatorcontrib><creatorcontrib>SICARD, A.-M</creatorcontrib><creatorcontrib>CLAVERYS, J.-P</creatorcontrib><collection>Pascal-Francis</collection><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>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</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>GASC, A.-M</au><au>SICARD, A.-M</au><au>CLAVERYS, J.-P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Repair of single- and multiple-substitution mismatches during recombination in Streptococcus pneumoniae</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>1989</date><risdate>1989</risdate><volume>121</volume><issue>1</issue><spage>29</spage><epage>36</epage><pages>29-36</pages><issn>0016-6731</issn><issn>1943-2631</issn><eissn>1943-2631</eissn><coden>GENTAE</coden><abstract>The use as genetic markers, during transformation of Streptococcus pneumoniae, of 19 sequences differing from wild type, located throughout the amiA locus, enabled us to examine the fate of 24 single- and 11 multiple-mismatches during recombination. Tentative mismatch ranking as a function of decreasing repair efficiency by the Hex mismatch repair system is G/T = A/C = G/G (maximum repair: 90-95%) greater than C/T (mostly 75 to 90% repair) greater than A/A (from 50 to 90% repair) greater than T/T (50-65% repair) greater than A/G (from 0 to 20% repair) greater than C/C. No indication of correction of the latter has been obtained. Over the limited number of samples examined, we observed no influence of the base composition of the surrounding sequence on correction efficiency for both transition mismatches and for G/G and C/C. Variations in the surrounding sequence affect repair of A/G and C/T, and, even more strongly, of A/A and T/T. No simple correlation to the G:C content of the surrounding sequence is apparent from our results, in contrast to the conclusion drawn for the Mut mismatch repair system of Escherichia coli. Examination of the fate of multiple mismatches suggests that C/C may sometimes impede recognition of otherwise corrected mismatches.</abstract><cop>Bethesda, MD</cop><pub>Genetics Society of America</pub><pmid>2645195</pmid><doi>10.1093/genetics/121.1.29</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | Freely Accessible Science Journals - check A-Z of ejournals; Alma/SFX Local Collection |
subjects | Base Composition Biological and medical sciences DNA Repair DNA, Bacterial - genetics Escherichia coli - genetics Fundamental and applied biological sciences. Psychology Genetic Markers Investigations Molecular and cellular biology Molecular genetics Mutagenesis. Repair Recombination, Genetic Streptococcus pneumoniae Streptococcus pneumoniae - genetics Transformation, Bacterial |
title | Repair of single- and multiple-substitution mismatches during recombination in Streptococcus pneumoniae |
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