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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)
Main Authors: Beck, Heather J, Janssen, Gary R
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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.
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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. 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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. 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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. 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source PubMed Central (Open Access); American Society for Microbiology Journals
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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