Tertiary interactions between helices h13 and h44 in 16S RNA contribute to the fidelity of translation
The A‐minor interaction, formed between single‐stranded adenosines and the minor groove of a receptor helix, is among the most common motifs found in rRNA. Among the A‐minors found in 16S rRNA are a set of interactions between adenosines at positions 1433, 1434 and 1468 in helix 44 (h44) and their r...
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description | The A‐minor interaction, formed between single‐stranded adenosines and the minor groove of a receptor helix, is among the most common motifs found in rRNA. Among the A‐minors found in 16S rRNA are a set of interactions between adenosines at positions 1433, 1434 and 1468 in helix 44 (h44) and their receptors in the nucleotide 320–340 region of helix 13 (h13). These interactions have been implicated in the maintenance of translational accuracy, because base substitutions at the adjacent C1469 increase miscoding errors. We have tested their functional significance through mutagenesis of h13 and h44. Mutations at the h44 A residues, or the A‐minor receptors in h13, increase a variety of translational errors and a subset of the mutants show decreased association between 30S and 50S ribosomal subunits. These results are consistent with the involvement of h13–h44 interactions in the alignment and packing of these helices in the 30S subunit and the importance of this helical alignment for tRNA selection and subunit–subunit interaction.
A series of RNA‐RNA interactions is formed between A1433, A1434 and A1468 in helix 44 of 16S ribosomal RNA and the nt 320–340 region of helix 13. Mutations in h44 or h13 residues increase a variety of translational errors, consistent with the involvement of h13‐h44 interactions in the alignment and packing of these helices in the 30S ribosomal subunit |
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A series of RNA‐RNA interactions is formed between A1433, A1434 and A1468 in helix 44 of 16S ribosomal RNA and the nt 320–340 region of helix 13. Mutations in h44 or h13 residues increase a variety of translational errors, consistent with the involvement of h13‐h44 interactions in the alignment and packing of these helices in the 30S ribosomal subunit</description><identifier>ISSN: 1742-464X</identifier><identifier>EISSN: 1742-4658</identifier><identifier>DOI: 10.1111/j.1742-4658.2011.08363.x</identifier><identifier>PMID: 21951637</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenosine ; A‐minor ; decoding ; Mutagenesis ; Mutation ; Mutation - genetics ; Nucleic Acid Conformation ; Protein Biosynthesis ; Ribonucleic acid ; ribosome ; Ribosomes - chemistry ; Ribosomes - metabolism ; RNA ; RNA, Bacterial - genetics ; RNA, Bacterial - metabolism ; RNA, Ribosomal, 16S - chemistry ; RNA, Ribosomal, 16S - genetics ; RNA, Ribosomal, 16S - metabolism ; rRNA</subject><ispartof>The FEBS journal, 2011-11, Vol.278 (22), p.4405-4412</ispartof><rights>2011 The Authors Journal compilation © 2011 FEBS</rights><rights>2011 The Authors Journal compilation © 2011 FEBS.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4293-8b91ed24858b65471da889222fbca9d6311601d59c5d93e3a8872a0025d125983</citedby><cites>FETCH-LOGICAL-c4293-8b91ed24858b65471da889222fbca9d6311601d59c5d93e3a8872a0025d125983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1742-4658.2011.08363.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1742-4658.2011.08363.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,1432,27922,27923,45572,45573,46407,46831</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21951637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tran, Diem K.</creatorcontrib><creatorcontrib>Finley, Jason</creatorcontrib><creatorcontrib>Vila‐Sanjurjo, Antón</creatorcontrib><creatorcontrib>Lale, Ajit</creatorcontrib><creatorcontrib>Sun, Qing</creatorcontrib><creatorcontrib>O’Connor, Michael</creatorcontrib><title>Tertiary interactions between helices h13 and h44 in 16S RNA contribute to the fidelity of translation</title><title>The FEBS journal</title><addtitle>FEBS J</addtitle><description>The A‐minor interaction, formed between single‐stranded adenosines and the minor groove of a receptor helix, is among the most common motifs found in rRNA. Among the A‐minors found in 16S rRNA are a set of interactions between adenosines at positions 1433, 1434 and 1468 in helix 44 (h44) and their receptors in the nucleotide 320–340 region of helix 13 (h13). These interactions have been implicated in the maintenance of translational accuracy, because base substitutions at the adjacent C1469 increase miscoding errors. We have tested their functional significance through mutagenesis of h13 and h44. Mutations at the h44 A residues, or the A‐minor receptors in h13, increase a variety of translational errors and a subset of the mutants show decreased association between 30S and 50S ribosomal subunits. These results are consistent with the involvement of h13–h44 interactions in the alignment and packing of these helices in the 30S subunit and the importance of this helical alignment for tRNA selection and subunit–subunit interaction.
A series of RNA‐RNA interactions is formed between A1433, A1434 and A1468 in helix 44 of 16S ribosomal RNA and the nt 320–340 region of helix 13. Mutations in h44 or h13 residues increase a variety of translational errors, consistent with the involvement of h13‐h44 interactions in the alignment and packing of these helices in the 30S ribosomal subunit</description><subject>Adenosine</subject><subject>A‐minor</subject><subject>decoding</subject><subject>Mutagenesis</subject><subject>Mutation</subject><subject>Mutation - genetics</subject><subject>Nucleic Acid Conformation</subject><subject>Protein Biosynthesis</subject><subject>Ribonucleic acid</subject><subject>ribosome</subject><subject>Ribosomes - chemistry</subject><subject>Ribosomes - metabolism</subject><subject>RNA</subject><subject>RNA, Bacterial - genetics</subject><subject>RNA, Bacterial - metabolism</subject><subject>RNA, Ribosomal, 16S - chemistry</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>RNA, Ribosomal, 16S - metabolism</subject><subject>rRNA</subject><issn>1742-464X</issn><issn>1742-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtr3DAUhUVpaR7tXyiiq27G1dXDljaFNCRpIbTQJNCdkK1rRoPHTiWZZP595Ew6i66qjS7c7xwu5xBCgVVQ3udNBY3kK1krXXEGUDEtalE9viLHh8Xrwyx_H5GTlDaMCSWNeUuOOBgFtWiOSX-LMQcXdzSMGaPrcpjGRFvMD4gjXeMQOkx0DYK60dO1lAWkUN_QXz_OaDeNOYZ2zkjzRPMaaR98keQdnXqaoxvT4BbHd-RN74aE71_-U3J3eXF7_m11_fPq-_nZ9aqT3IiVbg2g51Ir3dZKNuCd1oZz3redM74WADUDr0ynvBEoyrbhjjGuPHBltDgln_a-93H6M2PKdhtSh8PgRpzmZIHxkg2Ipinox3_QzTTHsVxnDYPGgOBQIL2HujilFLG39zFsS1zFyS5V2I1dUrZL4napwj5XYR-L9MOL_9xu0R-Ef7MvwJc98BAG3P23sb28-HqzjOIJaUCVMw</recordid><startdate>201111</startdate><enddate>201111</enddate><creator>Tran, Diem K.</creator><creator>Finley, Jason</creator><creator>Vila‐Sanjurjo, Antón</creator><creator>Lale, Ajit</creator><creator>Sun, Qing</creator><creator>O’Connor, Michael</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></search><sort><creationdate>201111</creationdate><title>Tertiary interactions between helices h13 and h44 in 16S RNA contribute to the fidelity of translation</title><author>Tran, Diem K. ; Finley, Jason ; Vila‐Sanjurjo, Antón ; Lale, Ajit ; Sun, Qing ; O’Connor, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4293-8b91ed24858b65471da889222fbca9d6311601d59c5d93e3a8872a0025d125983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adenosine</topic><topic>A‐minor</topic><topic>decoding</topic><topic>Mutagenesis</topic><topic>Mutation</topic><topic>Mutation - genetics</topic><topic>Nucleic Acid Conformation</topic><topic>Protein Biosynthesis</topic><topic>Ribonucleic acid</topic><topic>ribosome</topic><topic>Ribosomes - chemistry</topic><topic>Ribosomes - metabolism</topic><topic>RNA</topic><topic>RNA, Bacterial - genetics</topic><topic>RNA, Bacterial - metabolism</topic><topic>RNA, Ribosomal, 16S - chemistry</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>RNA, Ribosomal, 16S - metabolism</topic><topic>rRNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tran, Diem K.</creatorcontrib><creatorcontrib>Finley, Jason</creatorcontrib><creatorcontrib>Vila‐Sanjurjo, Antón</creatorcontrib><creatorcontrib>Lale, Ajit</creatorcontrib><creatorcontrib>Sun, Qing</creatorcontrib><creatorcontrib>O’Connor, Michael</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><jtitle>The FEBS journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tran, Diem K.</au><au>Finley, Jason</au><au>Vila‐Sanjurjo, Antón</au><au>Lale, Ajit</au><au>Sun, Qing</au><au>O’Connor, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tertiary interactions between helices h13 and h44 in 16S RNA contribute to the fidelity of translation</atitle><jtitle>The FEBS journal</jtitle><addtitle>FEBS J</addtitle><date>2011-11</date><risdate>2011</risdate><volume>278</volume><issue>22</issue><spage>4405</spage><epage>4412</epage><pages>4405-4412</pages><issn>1742-464X</issn><eissn>1742-4658</eissn><abstract>The A‐minor interaction, formed between single‐stranded adenosines and the minor groove of a receptor helix, is among the most common motifs found in rRNA. Among the A‐minors found in 16S rRNA are a set of interactions between adenosines at positions 1433, 1434 and 1468 in helix 44 (h44) and their receptors in the nucleotide 320–340 region of helix 13 (h13). These interactions have been implicated in the maintenance of translational accuracy, because base substitutions at the adjacent C1469 increase miscoding errors. We have tested their functional significance through mutagenesis of h13 and h44. Mutations at the h44 A residues, or the A‐minor receptors in h13, increase a variety of translational errors and a subset of the mutants show decreased association between 30S and 50S ribosomal subunits. These results are consistent with the involvement of h13–h44 interactions in the alignment and packing of these helices in the 30S subunit and the importance of this helical alignment for tRNA selection and subunit–subunit interaction.
A series of RNA‐RNA interactions is formed between A1433, A1434 and A1468 in helix 44 of 16S ribosomal RNA and the nt 320–340 region of helix 13. Mutations in h44 or h13 residues increase a variety of translational errors, consistent with the involvement of h13‐h44 interactions in the alignment and packing of these helices in the 30S ribosomal subunit</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21951637</pmid><doi>10.1111/j.1742-4658.2011.08363.x</doi><tpages>8</tpages></addata></record> |
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subjects | Adenosine A‐minor decoding Mutagenesis Mutation Mutation - genetics Nucleic Acid Conformation Protein Biosynthesis Ribonucleic acid ribosome Ribosomes - chemistry Ribosomes - metabolism RNA RNA, Bacterial - genetics RNA, Bacterial - metabolism RNA, Ribosomal, 16S - chemistry RNA, Ribosomal, 16S - genetics RNA, Ribosomal, 16S - metabolism rRNA |
title | Tertiary interactions between helices h13 and h44 in 16S RNA contribute to the fidelity of translation |
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