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Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases
DNA templates containing a set of base modifications in the major groove (5-substituted pyrimidines or 7-substituted 7-deazapurines bearing H, methyl, vinyl, ethynyl or phenyl groups) were prepared by PCR using the corresponding base-modified 2'-deoxyribonucleoside triphosphates (dNTPs). The mo...
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Published in: | Nucleic acids research 2016-04, Vol.44 (7), p.3000-3012 |
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creator | Raindlová, Veronika Janoušková, Martina Slavíčková, Michaela Perlíková, Pavla Boháčová, Soňa Milisavljevič, Nemanja Šanderová, Hana Benda, Martin Barvík, Ivan Krásný, Libor Hocek, Michal |
description | DNA templates containing a set of base modifications in the major groove (5-substituted pyrimidines or 7-substituted 7-deazapurines bearing H, methyl, vinyl, ethynyl or phenyl groups) were prepared by PCR using the corresponding base-modified 2'-deoxyribonucleoside triphosphates (dNTPs). The modified templates were used in an in vitro transcription assay using RNA polymerase from Bacillus subtilis and Escherichia coli Some modified nucleobases bearing smaller modifications (H, Me in 7-deazapurines) were perfectly tolerated by both enzymes, whereas bulky modifications (Ph at any nucleobase) and, surprisingly, uracil blocked transcription. Some middle-sized modifications (vinyl or ethynyl) were partly tolerated mostly by the E. colienzyme. In all cases where the transcription proceeded, full length RNA product with correct sequence was obtained indicating that the modifications of the template are not mutagenic and the inhibition is probably at the stage of initiation. The results are promising for the development of bioorthogonal reactions for artificial chemical switching of the transcription. |
doi_str_mv | 10.1093/nar/gkw171 |
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The modified templates were used in an in vitro transcription assay using RNA polymerase from Bacillus subtilis and Escherichia coli Some modified nucleobases bearing smaller modifications (H, Me in 7-deazapurines) were perfectly tolerated by both enzymes, whereas bulky modifications (Ph at any nucleobase) and, surprisingly, uracil blocked transcription. Some middle-sized modifications (vinyl or ethynyl) were partly tolerated mostly by the E. colienzyme. In all cases where the transcription proceeded, full length RNA product with correct sequence was obtained indicating that the modifications of the template are not mutagenic and the inhibition is probably at the stage of initiation. The results are promising for the development of bioorthogonal reactions for artificial chemical switching of the transcription.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkw171</identifier><identifier>PMID: 27001521</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Bacillus subtilis ; Bacillus subtilis - enzymology ; Chemical Biology and Nucleic Acid Chemistry ; Deoxyribonucleotides - biosynthesis ; Deoxyribonucleotides - chemistry ; DNA - chemistry ; DNA - metabolism ; DNA-Directed RNA Polymerases - metabolism ; Escherichia coli ; Escherichia coli - enzymology ; Nucleic Acid Conformation ; Templates, Genetic ; Transcription, Genetic</subject><ispartof>Nucleic acids research, 2016-04, Vol.44 (7), p.3000-3012</ispartof><rights>The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><rights>The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-ccb1f99c1c307931eb6e2f02d4e397dac236585c845112470162910e7d9ffafd3</citedby><cites>FETCH-LOGICAL-c411t-ccb1f99c1c307931eb6e2f02d4e397dac236585c845112470162910e7d9ffafd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838386/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838386/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27001521$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raindlová, Veronika</creatorcontrib><creatorcontrib>Janoušková, Martina</creatorcontrib><creatorcontrib>Slavíčková, Michaela</creatorcontrib><creatorcontrib>Perlíková, Pavla</creatorcontrib><creatorcontrib>Boháčová, Soňa</creatorcontrib><creatorcontrib>Milisavljevič, Nemanja</creatorcontrib><creatorcontrib>Šanderová, Hana</creatorcontrib><creatorcontrib>Benda, Martin</creatorcontrib><creatorcontrib>Barvík, Ivan</creatorcontrib><creatorcontrib>Krásný, Libor</creatorcontrib><creatorcontrib>Hocek, Michal</creatorcontrib><title>Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>DNA templates containing a set of base modifications in the major groove (5-substituted pyrimidines or 7-substituted 7-deazapurines bearing H, methyl, vinyl, ethynyl or phenyl groups) were prepared by PCR using the corresponding base-modified 2'-deoxyribonucleoside triphosphates (dNTPs). 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The results are promising for the development of bioorthogonal reactions for artificial chemical switching of the transcription.</description><subject>Bacillus subtilis</subject><subject>Bacillus subtilis - enzymology</subject><subject>Chemical Biology and Nucleic Acid Chemistry</subject><subject>Deoxyribonucleotides - biosynthesis</subject><subject>Deoxyribonucleotides - chemistry</subject><subject>DNA - chemistry</subject><subject>DNA - metabolism</subject><subject>DNA-Directed RNA Polymerases - metabolism</subject><subject>Escherichia coli</subject><subject>Escherichia coli - enzymology</subject><subject>Nucleic Acid Conformation</subject><subject>Templates, Genetic</subject><subject>Transcription, Genetic</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkU9r3DAQxUVoaLZpL_kAxccScKKRZMu6FEL-tIGQQmnPQpZHG6W2tJW8Kfvto2XTkNzCHGZgfvN4wyPkCOgJUMVPg0mnyz__QMIeWQBvWS1Uy96RBeW0qYGK7oB8yPmeUhDQiPfkgMkyNwwWBK-DG9cYLFbRVZO5j6lephgfsLJ3OHlrxmqKg3dlmn0MeYtd3J5VMVRzMiHb5FfbRdVvqt7YGZMvJz8LsYrjZsJkMuaPZN-ZMeOnp35Ifl9d_jr_Xt_8-HZ9fnZTWwEw19b24JSyYDmVigP2LTJH2SCQKzkYy3jbdI3tRAPAhKTQMgUU5aCcM27gh-TrTne17iccLIbicdSr5CeTNjoar19vgr_Ty_igRcdLtUXgy5NAin_XmGc9-WxxHE3AuM4aZCeVbGQLb0G5AkHZVvV4h9oUc07onh0B1dsIdYlQ7yIs8OeXPzyj_zPjjxDVma4</recordid><startdate>20160420</startdate><enddate>20160420</enddate><creator>Raindlová, Veronika</creator><creator>Janoušková, Martina</creator><creator>Slavíčková, Michaela</creator><creator>Perlíková, Pavla</creator><creator>Boháčová, Soňa</creator><creator>Milisavljevič, Nemanja</creator><creator>Šanderová, Hana</creator><creator>Benda, Martin</creator><creator>Barvík, Ivan</creator><creator>Krásný, Libor</creator><creator>Hocek, Michal</creator><general>Oxford University Press</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>7X8</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20160420</creationdate><title>Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases</title><author>Raindlová, Veronika ; Janoušková, Martina ; Slavíčková, Michaela ; Perlíková, Pavla ; Boháčová, Soňa ; Milisavljevič, Nemanja ; Šanderová, Hana ; Benda, Martin ; Barvík, Ivan ; Krásný, Libor ; Hocek, Michal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-ccb1f99c1c307931eb6e2f02d4e397dac236585c845112470162910e7d9ffafd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Bacillus subtilis</topic><topic>Bacillus subtilis - enzymology</topic><topic>Chemical Biology and Nucleic Acid Chemistry</topic><topic>Deoxyribonucleotides - biosynthesis</topic><topic>Deoxyribonucleotides - chemistry</topic><topic>DNA - chemistry</topic><topic>DNA - metabolism</topic><topic>DNA-Directed RNA Polymerases - metabolism</topic><topic>Escherichia coli</topic><topic>Escherichia coli - enzymology</topic><topic>Nucleic Acid Conformation</topic><topic>Templates, Genetic</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raindlová, Veronika</creatorcontrib><creatorcontrib>Janoušková, Martina</creatorcontrib><creatorcontrib>Slavíčková, Michaela</creatorcontrib><creatorcontrib>Perlíková, Pavla</creatorcontrib><creatorcontrib>Boháčová, Soňa</creatorcontrib><creatorcontrib>Milisavljevič, Nemanja</creatorcontrib><creatorcontrib>Šanderová, Hana</creatorcontrib><creatorcontrib>Benda, Martin</creatorcontrib><creatorcontrib>Barvík, Ivan</creatorcontrib><creatorcontrib>Krásný, Libor</creatorcontrib><creatorcontrib>Hocek, Michal</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raindlová, Veronika</au><au>Janoušková, Martina</au><au>Slavíčková, Michaela</au><au>Perlíková, Pavla</au><au>Boháčová, Soňa</au><au>Milisavljevič, Nemanja</au><au>Šanderová, Hana</au><au>Benda, Martin</au><au>Barvík, Ivan</au><au>Krásný, Libor</au><au>Hocek, Michal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2016-04-20</date><risdate>2016</risdate><volume>44</volume><issue>7</issue><spage>3000</spage><epage>3012</epage><pages>3000-3012</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>DNA templates containing a set of base modifications in the major groove (5-substituted pyrimidines or 7-substituted 7-deazapurines bearing H, methyl, vinyl, ethynyl or phenyl groups) were prepared by PCR using the corresponding base-modified 2'-deoxyribonucleoside triphosphates (dNTPs). 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subjects | Bacillus subtilis Bacillus subtilis - enzymology Chemical Biology and Nucleic Acid Chemistry Deoxyribonucleotides - biosynthesis Deoxyribonucleotides - chemistry DNA - chemistry DNA - metabolism DNA-Directed RNA Polymerases - metabolism Escherichia coli Escherichia coli - enzymology Nucleic Acid Conformation Templates, Genetic Transcription, Genetic |
title | Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases |
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