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Novel Translation Initiation Regulation Mechanism in Escherichia coli ptrB Mediated by a 5'-Terminal AUG
Alternative translation initiation mechanisms, distinct from the Shine-Dalgarno (SD) sequence-dependent mechanism, are more prevalent in bacteria than once anticipated. Translation of instead requires an AUG triplet at the 5' terminus of its mRNA. The 5'-terminal AUG (5'-uAUG) acts as...
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Published in: | Journal of bacteriology 2017-07, Vol.199 (14) |
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description | Alternative translation initiation mechanisms, distinct from the Shine-Dalgarno (SD) sequence-dependent mechanism, are more prevalent in bacteria than once anticipated. Translation of
instead requires an AUG triplet at the 5' terminus of its mRNA. The 5'-terminal AUG (5'-uAUG) acts as a ribosomal recognition signal to attract ribosomes to the
mRNA rather than functioning as an initiation codon to support translation of an upstream open reading frame.
expression exhibits a stronger dependence on the 5'-uAUG than the predicted SD sequence; however, strengthening the predicted
SD sequence relieves the necessity for the 5'-uAUG. Additional sequences within the
5' untranslated region (5'-UTR) work cumulatively with the 5'-uAUG to control expression of the downstream
coding sequence (CDS), thereby compensating for the weak SD sequence. Replacement of 5'-UTRs from other mRNAs with the
5'-UTR sequence showed a similar dependence on the 5'-uAUG for CDS expression, suggesting that the regulatory features contained within the
5'-UTR are sufficient to control the expression of other
CDSs. Demonstration that the 5'-uAUG present on the
leader mRNA is involved in ribosome binding and expression of the downstream
CDS revealed a novel form of translational regulation. Due to the abundance of AUG triplets at the 5' termini of
mRNAs and the ability of
5'-UTR regulation to function independently of gene context, the regulatory effects of 5'-uAUGs on downstream CDSs may be widespread throughout the
genome.
As the field of synthetic biology continues to grow, a complete understanding of basic biological principles will be necessary. The increasing complexity of the synthetic systems highlights the gaps in our current knowledge of RNA regulation. This study demonstrates that there are novel ways to regulate canonical Shine-Dalgarno-led mRNAs in
, illustrating that our understanding of the fundamental processes of translation and RNA regulation is still incomplete. Even for
, one of the most-studied model organisms, genes with translation initiation mechanisms that do not fit the canonical Shine-Dalgarno sequence paradigm are being revealed. Uncovering diverse mechanisms that control translational expression will allow synthetic biologists to finely tune protein production of desired gene products. |
doi_str_mv | 10.1128/JB.00091-17 |
format | article |
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instead requires an AUG triplet at the 5' terminus of its mRNA. The 5'-terminal AUG (5'-uAUG) acts as a ribosomal recognition signal to attract ribosomes to the
mRNA rather than functioning as an initiation codon to support translation of an upstream open reading frame.
expression exhibits a stronger dependence on the 5'-uAUG than the predicted SD sequence; however, strengthening the predicted
SD sequence relieves the necessity for the 5'-uAUG. Additional sequences within the
5' untranslated region (5'-UTR) work cumulatively with the 5'-uAUG to control expression of the downstream
coding sequence (CDS), thereby compensating for the weak SD sequence. Replacement of 5'-UTRs from other mRNAs with the
5'-UTR sequence showed a similar dependence on the 5'-uAUG for CDS expression, suggesting that the regulatory features contained within the
5'-UTR are sufficient to control the expression of other
CDSs. Demonstration that the 5'-uAUG present on the
leader mRNA is involved in ribosome binding and expression of the downstream
CDS revealed a novel form of translational regulation. Due to the abundance of AUG triplets at the 5' termini of
mRNAs and the ability of
5'-UTR regulation to function independently of gene context, the regulatory effects of 5'-uAUGs on downstream CDSs may be widespread throughout the
genome.
As the field of synthetic biology continues to grow, a complete understanding of basic biological principles will be necessary. The increasing complexity of the synthetic systems highlights the gaps in our current knowledge of RNA regulation. This study demonstrates that there are novel ways to regulate canonical Shine-Dalgarno-led mRNAs in
, illustrating that our understanding of the fundamental processes of translation and RNA regulation is still incomplete. Even for
, one of the most-studied model organisms, genes with translation initiation mechanisms that do not fit the canonical Shine-Dalgarno sequence paradigm are being revealed. Uncovering diverse mechanisms that control translational expression will allow synthetic biologists to finely tune protein production of desired gene products.</description><identifier>ISSN: 0021-9193</identifier><identifier>EISSN: 1098-5530</identifier><identifier>DOI: 10.1128/JB.00091-17</identifier><identifier>PMID: 28484048</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>5' Untranslated Regions ; Abundance ; Bacteriology ; E coli ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Gene Expression Regulation, Bacterial - physiology ; Genomes ; Metalloendopeptidases - genetics ; Metalloendopeptidases - metabolism ; mRNA ; Nucleic Acid Conformation ; Peptide Chain Initiation, Translational - physiology ; Protein Binding ; Ribonucleic acid ; Ribosomes ; RNA ; RNA Caps - physiology ; RNA, Bacterial - genetics ; RNA, Bacterial - metabolism ; RNA, Messenger - chemistry ; RNA, Messenger - metabolism ; Translation ; Translation initiation</subject><ispartof>Journal of bacteriology, 2017-07, Vol.199 (14)</ispartof><rights>Copyright © 2017 American Society for Microbiology.</rights><rights>Copyright American Society for Microbiology Jul 2017</rights><rights>Copyright © 2017 American Society for Microbiology. 2017 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-22948d36e4982e99d652ccf771a307ce636ca72addf33e851ce40e9056528bbb3</citedby><cites>FETCH-LOGICAL-c409t-22948d36e4982e99d652ccf771a307ce636ca72addf33e851ce40e9056528bbb3</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/PMC5494737/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494737/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28484048$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Henkin, Tina M.</contributor><creatorcontrib>Beck, Heather J</creatorcontrib><creatorcontrib>Janssen, Gary R</creatorcontrib><title>Novel Translation Initiation Regulation Mechanism in Escherichia coli ptrB Mediated by a 5'-Terminal AUG</title><title>Journal of bacteriology</title><addtitle>J Bacteriol</addtitle><description>Alternative translation initiation mechanisms, distinct from the Shine-Dalgarno (SD) sequence-dependent mechanism, are more prevalent in bacteria than once anticipated. Translation of
instead requires an AUG triplet at the 5' terminus of its mRNA. The 5'-terminal AUG (5'-uAUG) acts as a ribosomal recognition signal to attract ribosomes to the
mRNA rather than functioning as an initiation codon to support translation of an upstream open reading frame.
expression exhibits a stronger dependence on the 5'-uAUG than the predicted SD sequence; however, strengthening the predicted
SD sequence relieves the necessity for the 5'-uAUG. Additional sequences within the
5' untranslated region (5'-UTR) work cumulatively with the 5'-uAUG to control expression of the downstream
coding sequence (CDS), thereby compensating for the weak SD sequence. Replacement of 5'-UTRs from other mRNAs with the
5'-UTR sequence showed a similar dependence on the 5'-uAUG for CDS expression, suggesting that the regulatory features contained within the
5'-UTR are sufficient to control the expression of other
CDSs. Demonstration that the 5'-uAUG present on the
leader mRNA is involved in ribosome binding and expression of the downstream
CDS revealed a novel form of translational regulation. Due to the abundance of AUG triplets at the 5' termini of
mRNAs and the ability of
5'-UTR regulation to function independently of gene context, the regulatory effects of 5'-uAUGs on downstream CDSs may be widespread throughout the
genome.
As the field of synthetic biology continues to grow, a complete understanding of basic biological principles will be necessary. The increasing complexity of the synthetic systems highlights the gaps in our current knowledge of RNA regulation. This study demonstrates that there are novel ways to regulate canonical Shine-Dalgarno-led mRNAs in
, illustrating that our understanding of the fundamental processes of translation and RNA regulation is still incomplete. Even for
, one of the most-studied model organisms, genes with translation initiation mechanisms that do not fit the canonical Shine-Dalgarno sequence paradigm are being revealed. Uncovering diverse mechanisms that control translational expression will allow synthetic biologists to finely tune protein production of desired gene products.</description><subject>5' Untranslated Regions</subject><subject>Abundance</subject><subject>Bacteriology</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Gene Expression Regulation, Bacterial - physiology</subject><subject>Genomes</subject><subject>Metalloendopeptidases - genetics</subject><subject>Metalloendopeptidases - metabolism</subject><subject>mRNA</subject><subject>Nucleic Acid Conformation</subject><subject>Peptide Chain Initiation, Translational - physiology</subject><subject>Protein Binding</subject><subject>Ribonucleic acid</subject><subject>Ribosomes</subject><subject>RNA</subject><subject>RNA Caps - physiology</subject><subject>RNA, Bacterial - genetics</subject><subject>RNA, Bacterial - metabolism</subject><subject>RNA, Messenger - chemistry</subject><subject>RNA, Messenger - metabolism</subject><subject>Translation</subject><subject>Translation initiation</subject><issn>0021-9193</issn><issn>1098-5530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpdkd9LHDEQx0Op1KvtU99LoA8KZW1-7iYvBU-sVWwL5XwO2eycG9lNrsmu4H_f6F2l-jTDzGe-M8MXoQ-UHFPK1JfL5TEhRNOKNq_QghKtKik5eY0WhDBaaar5Pnqb8y0hVAjJ3qB9poQSRKgF6n_GOxjwKtmQBzv5GPBF8JPfpr_hZt5Vf4DrbfB5xD7gs-x6SN713mIXB483U1oWpCtz0OH2HlssD6sVpNEHO-CT6_N3aG9thwzvd_EAXX87W51-r65-nV-cnlxVThA9VYxpoTpeg9CKgdZdLZlz66ahlpPGQc1rZxtmu27NOShJHQgCmsjCqbZt-QH6utXdzO0InYMwJTuYTfKjTfcmWm-ed4LvzU28M1Jo0fCmCBztBFL8M0OezOizg2GwAeKcDVW6VlrWShX00wv0Ns6pPFwoXSxgTGlSqM9byqWYc4L10zGUmAcHzeXSPDpo6MP6j__f_8T-s4z_BfF6leI</recordid><startdate>20170715</startdate><enddate>20170715</enddate><creator>Beck, Heather J</creator><creator>Janssen, Gary R</creator><general>American Society for Microbiology</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>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><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170715</creationdate><title>Novel Translation Initiation Regulation Mechanism in Escherichia coli ptrB Mediated by a 5'-Terminal AUG</title><author>Beck, Heather J ; Janssen, Gary R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-22948d36e4982e99d652ccf771a307ce636ca72addf33e851ce40e9056528bbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>5' Untranslated Regions</topic><topic>Abundance</topic><topic>Bacteriology</topic><topic>E coli</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Gene Expression Regulation, Bacterial - physiology</topic><topic>Genomes</topic><topic>Metalloendopeptidases - genetics</topic><topic>Metalloendopeptidases - metabolism</topic><topic>mRNA</topic><topic>Nucleic Acid Conformation</topic><topic>Peptide Chain Initiation, Translational - physiology</topic><topic>Protein Binding</topic><topic>Ribonucleic acid</topic><topic>Ribosomes</topic><topic>RNA</topic><topic>RNA Caps - physiology</topic><topic>RNA, Bacterial - genetics</topic><topic>RNA, Bacterial - metabolism</topic><topic>RNA, Messenger - chemistry</topic><topic>RNA, Messenger - metabolism</topic><topic>Translation</topic><topic>Translation initiation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beck, Heather J</creatorcontrib><creatorcontrib>Janssen, Gary R</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>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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bacteriology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beck, Heather J</au><au>Janssen, Gary R</au><au>Henkin, Tina M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel Translation Initiation Regulation Mechanism in Escherichia coli ptrB Mediated by a 5'-Terminal AUG</atitle><jtitle>Journal of bacteriology</jtitle><addtitle>J Bacteriol</addtitle><date>2017-07-15</date><risdate>2017</risdate><volume>199</volume><issue>14</issue><issn>0021-9193</issn><eissn>1098-5530</eissn><abstract>Alternative translation initiation mechanisms, distinct from the Shine-Dalgarno (SD) sequence-dependent mechanism, are more prevalent in bacteria than once anticipated. Translation of
instead requires an AUG triplet at the 5' terminus of its mRNA. The 5'-terminal AUG (5'-uAUG) acts as a ribosomal recognition signal to attract ribosomes to the
mRNA rather than functioning as an initiation codon to support translation of an upstream open reading frame.
expression exhibits a stronger dependence on the 5'-uAUG than the predicted SD sequence; however, strengthening the predicted
SD sequence relieves the necessity for the 5'-uAUG. Additional sequences within the
5' untranslated region (5'-UTR) work cumulatively with the 5'-uAUG to control expression of the downstream
coding sequence (CDS), thereby compensating for the weak SD sequence. Replacement of 5'-UTRs from other mRNAs with the
5'-UTR sequence showed a similar dependence on the 5'-uAUG for CDS expression, suggesting that the regulatory features contained within the
5'-UTR are sufficient to control the expression of other
CDSs. Demonstration that the 5'-uAUG present on the
leader mRNA is involved in ribosome binding and expression of the downstream
CDS revealed a novel form of translational regulation. Due to the abundance of AUG triplets at the 5' termini of
mRNAs and the ability of
5'-UTR regulation to function independently of gene context, the regulatory effects of 5'-uAUGs on downstream CDSs may be widespread throughout the
genome.
As the field of synthetic biology continues to grow, a complete understanding of basic biological principles will be necessary. The increasing complexity of the synthetic systems highlights the gaps in our current knowledge of RNA regulation. This study demonstrates that there are novel ways to regulate canonical Shine-Dalgarno-led mRNAs in
, illustrating that our understanding of the fundamental processes of translation and RNA regulation is still incomplete. Even for
, one of the most-studied model organisms, genes with translation initiation mechanisms that do not fit the canonical Shine-Dalgarno sequence paradigm are being revealed. Uncovering diverse mechanisms that control translational expression will allow synthetic biologists to finely tune protein production of desired gene products.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>28484048</pmid><doi>10.1128/JB.00091-17</doi><oa>free_for_read</oa></addata></record> |
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subjects | 5' Untranslated Regions Abundance Bacteriology E coli Escherichia coli Escherichia coli - genetics Escherichia coli - metabolism Gene Expression Regulation, Bacterial - physiology Genomes Metalloendopeptidases - genetics Metalloendopeptidases - metabolism mRNA Nucleic Acid Conformation Peptide Chain Initiation, Translational - physiology Protein Binding Ribonucleic acid Ribosomes RNA RNA Caps - physiology RNA, Bacterial - genetics RNA, Bacterial - metabolism RNA, Messenger - chemistry RNA, Messenger - metabolism Translation Translation initiation |
title | Novel Translation Initiation Regulation Mechanism in Escherichia coli ptrB Mediated by a 5'-Terminal AUG |
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