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Identification of temperature-sensitive dnaD mutants of Staphylococcus aureus that are defective in chromosomal DNA replication
The DnaD protein in Gram-positive bacteria is thought to be essential for the initiation step in DNA replication. In the present study, we characterized two Staphylococcus aureus mutants whose temperature-sensitive growth phenotype could be complemented by a plasmid carrying the dnaD gene. These mut...
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Published in: | Molecular genetics and genomics : MGG 2004-05, Vol.271 (4), p.447-457 |
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description | The DnaD protein in Gram-positive bacteria is thought to be essential for the initiation step in DNA replication. In the present study, we characterized two Staphylococcus aureus mutants whose temperature-sensitive growth phenotype could be complemented by a plasmid carrying the dnaD gene. These mutants each had a single amino acid substitution in the DnaD protein and showed decreased DNA synthesis at restrictive temperature. Analyses of the origin to terminus ratio by Southern blotting, and of origin numbers per cell by flow cytometry, revealed that, at the restrictive temperature, one mutant continued ongoing DNA replication but failed to initiate DNA replication. The other mutant, in contrast, could not complete ongoing DNA replication and proceeded to degrade the chromosome. However, if protein synthesis was inhibited, the second mutant could complete DNA replication. These results suggest that DnaD protein is necessary not only for the initiation step, but also to avoid replication fork blockage. Moreover, both mutants were sensitive to mitomycin C, a drug that induces DNA damage, suggesting that the DnaD protein is also involved in DNA repair. |
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In the present study, we characterized two Staphylococcus aureus mutants whose temperature-sensitive growth phenotype could be complemented by a plasmid carrying the dnaD gene. These mutants each had a single amino acid substitution in the DnaD protein and showed decreased DNA synthesis at restrictive temperature. Analyses of the origin to terminus ratio by Southern blotting, and of origin numbers per cell by flow cytometry, revealed that, at the restrictive temperature, one mutant continued ongoing DNA replication but failed to initiate DNA replication. The other mutant, in contrast, could not complete ongoing DNA replication and proceeded to degrade the chromosome. However, if protein synthesis was inhibited, the second mutant could complete DNA replication. These results suggest that DnaD protein is necessary not only for the initiation step, but also to avoid replication fork blockage. Moreover, both mutants were sensitive to mitomycin C, a drug that induces DNA damage, suggesting that the DnaD protein is also involved in DNA repair.</description><identifier>ISSN: 1617-4615</identifier><identifier>EISSN: 1617-4623</identifier><identifier>DOI: 10.1007/s00438-004-0996-6</identifier><identifier>PMID: 15042355</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Amino Acid Substitution ; Bacterial Proteins - genetics ; Blotting, Southern ; Chromosomes, Bacterial - genetics ; Deoxyribonucleic acid ; DNA ; DNA Damage ; DNA Repair ; DNA Replication ; DNA, Bacterial - genetics ; DNA, Bacterial - metabolism ; DNA-Binding Proteins - deficiency ; DNA-Binding Proteins - genetics ; Flow Cytometry ; Genetics ; Mitomycin - pharmacology ; Mutation ; Nucleic Acid Synthesis Inhibitors - pharmacology ; Phenotype ; Proteins ; Staphylococcus aureus ; Staphylococcus aureus - genetics ; Staphylococcus aureus - growth & development ; Temperature</subject><ispartof>Molecular genetics and genomics : MGG, 2004-05, Vol.271 (4), p.447-457</ispartof><rights>Springer-Verlag 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c355t-84ff7c3c18c13f017362964c5427a7b4a10fbe25ecc76255b3adbeffcccbe39b3</citedby><cites>FETCH-LOGICAL-c355t-84ff7c3c18c13f017362964c5427a7b4a10fbe25ecc76255b3adbeffcccbe39b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15042355$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Y</creatorcontrib><creatorcontrib>Kurokawa, K</creatorcontrib><creatorcontrib>Matsuo, M</creatorcontrib><creatorcontrib>Fukuhara, N</creatorcontrib><creatorcontrib>Murakami, K</creatorcontrib><creatorcontrib>Sekimizu, K</creatorcontrib><title>Identification of temperature-sensitive dnaD mutants of Staphylococcus aureus that are defective in chromosomal DNA replication</title><title>Molecular genetics and genomics : MGG</title><addtitle>Mol Genet Genomics</addtitle><description>The DnaD protein in Gram-positive bacteria is thought to be essential for the initiation step in DNA replication. In the present study, we characterized two Staphylococcus aureus mutants whose temperature-sensitive growth phenotype could be complemented by a plasmid carrying the dnaD gene. These mutants each had a single amino acid substitution in the DnaD protein and showed decreased DNA synthesis at restrictive temperature. Analyses of the origin to terminus ratio by Southern blotting, and of origin numbers per cell by flow cytometry, revealed that, at the restrictive temperature, one mutant continued ongoing DNA replication but failed to initiate DNA replication. The other mutant, in contrast, could not complete ongoing DNA replication and proceeded to degrade the chromosome. However, if protein synthesis was inhibited, the second mutant could complete DNA replication. These results suggest that DnaD protein is necessary not only for the initiation step, but also to avoid replication fork blockage. Moreover, both mutants were sensitive to mitomycin C, a drug that induces DNA damage, suggesting that the DnaD protein is also involved in DNA repair.</description><subject>Amino Acid Substitution</subject><subject>Bacterial Proteins - genetics</subject><subject>Blotting, Southern</subject><subject>Chromosomes, Bacterial - genetics</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Damage</subject><subject>DNA Repair</subject><subject>DNA Replication</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Bacterial - metabolism</subject><subject>DNA-Binding Proteins - deficiency</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Flow Cytometry</subject><subject>Genetics</subject><subject>Mitomycin - pharmacology</subject><subject>Mutation</subject><subject>Nucleic Acid Synthesis Inhibitors - pharmacology</subject><subject>Phenotype</subject><subject>Proteins</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - genetics</subject><subject>Staphylococcus aureus - growth & development</subject><subject>Temperature</subject><issn>1617-4615</issn><issn>1617-4623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkU1P3DAQhq2qqHy0P6AXZPXALcUfsZ0cEQsUCcEBerac2bE2KImD7SBx6l-vl121Ui-9zMzheWfm1UvIV86-c8bMeWKslk1VasXaVlf6Aznimpuq1kJ-_DNzdUiOU3pmjBstzCdyyBWrhVTqiPy6XeOUe9-Dy32YaPA04zhjdHmJWCWcUp_7V6Trya3ouGQ35bSlHrObN29DgACwJOoKXVreuExdLDh6hHdhP1HYxDCGFEY30NX9BY04D_uDn8mBd0PCL_t-Qn5eXz1d_qjuHm5uLy_uKihv5qqpvTcggTfApS8-pBatrkHVwjjT1Y4z36FQCFAsKtVJt-7QewDoULadPCFnu71zDC8LpmzHPgEOg5swLMka3motRPtfkDdMK6ZlAb_9Az6HJU7FhG2YkY1Qpi4Q30EQQ0oRvZ1jP7r4Zjmz2wztLkNbqt1maHXRnO4XL92I67-KfWjyNzaVmes</recordid><startdate>200405</startdate><enddate>200405</enddate><creator>Li, Y</creator><creator>Kurokawa, K</creator><creator>Matsuo, M</creator><creator>Fukuhara, N</creator><creator>Murakami, K</creator><creator>Sekimizu, K</creator><general>Springer Nature B.V</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>3V.</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>200405</creationdate><title>Identification of temperature-sensitive dnaD mutants of Staphylococcus aureus that are defective in chromosomal DNA replication</title><author>Li, Y ; Kurokawa, K ; Matsuo, M ; Fukuhara, N ; Murakami, K ; Sekimizu, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c355t-84ff7c3c18c13f017362964c5427a7b4a10fbe25ecc76255b3adbeffcccbe39b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Amino Acid Substitution</topic><topic>Bacterial Proteins - genetics</topic><topic>Blotting, Southern</topic><topic>Chromosomes, Bacterial - genetics</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Damage</topic><topic>DNA Repair</topic><topic>DNA Replication</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Bacterial - metabolism</topic><topic>DNA-Binding Proteins - deficiency</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Flow Cytometry</topic><topic>Genetics</topic><topic>Mitomycin - pharmacology</topic><topic>Mutation</topic><topic>Nucleic Acid Synthesis Inhibitors - pharmacology</topic><topic>Phenotype</topic><topic>Proteins</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - genetics</topic><topic>Staphylococcus aureus - growth & development</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Y</creatorcontrib><creatorcontrib>Kurokawa, K</creatorcontrib><creatorcontrib>Matsuo, M</creatorcontrib><creatorcontrib>Fukuhara, N</creatorcontrib><creatorcontrib>Murakami, K</creatorcontrib><creatorcontrib>Sekimizu, K</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 Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular genetics and genomics : MGG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Y</au><au>Kurokawa, K</au><au>Matsuo, M</au><au>Fukuhara, N</au><au>Murakami, K</au><au>Sekimizu, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of temperature-sensitive dnaD mutants of Staphylococcus aureus that are defective in chromosomal DNA replication</atitle><jtitle>Molecular genetics and genomics : MGG</jtitle><addtitle>Mol Genet Genomics</addtitle><date>2004-05</date><risdate>2004</risdate><volume>271</volume><issue>4</issue><spage>447</spage><epage>457</epage><pages>447-457</pages><issn>1617-4615</issn><eissn>1617-4623</eissn><abstract>The DnaD protein in Gram-positive bacteria is thought to be essential for the initiation step in DNA replication. In the present study, we characterized two Staphylococcus aureus mutants whose temperature-sensitive growth phenotype could be complemented by a plasmid carrying the dnaD gene. These mutants each had a single amino acid substitution in the DnaD protein and showed decreased DNA synthesis at restrictive temperature. Analyses of the origin to terminus ratio by Southern blotting, and of origin numbers per cell by flow cytometry, revealed that, at the restrictive temperature, one mutant continued ongoing DNA replication but failed to initiate DNA replication. The other mutant, in contrast, could not complete ongoing DNA replication and proceeded to degrade the chromosome. However, if protein synthesis was inhibited, the second mutant could complete DNA replication. These results suggest that DnaD protein is necessary not only for the initiation step, but also to avoid replication fork blockage. Moreover, both mutants were sensitive to mitomycin C, a drug that induces DNA damage, suggesting that the DnaD protein is also involved in DNA repair.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>15042355</pmid><doi>10.1007/s00438-004-0996-6</doi><tpages>11</tpages></addata></record> |
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subjects | Amino Acid Substitution Bacterial Proteins - genetics Blotting, Southern Chromosomes, Bacterial - genetics Deoxyribonucleic acid DNA DNA Damage DNA Repair DNA Replication DNA, Bacterial - genetics DNA, Bacterial - metabolism DNA-Binding Proteins - deficiency DNA-Binding Proteins - genetics Flow Cytometry Genetics Mitomycin - pharmacology Mutation Nucleic Acid Synthesis Inhibitors - pharmacology Phenotype Proteins Staphylococcus aureus Staphylococcus aureus - genetics Staphylococcus aureus - growth & development Temperature |
title | Identification of temperature-sensitive dnaD mutants of Staphylococcus aureus that are defective in chromosomal DNA replication |
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