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dc.contributor.authorThiaville, Patrick C.
dc.contributor.authorEl Yacoubi, Basma
dc.contributor.authorThiaville, Jennifer J.
dc.contributor.authorDeutsch, Chris
dc.contributor.authorIwata-Reuyl, Dirk
dc.contributor.authorBacusmo, Jo Marie
dc.contributor.authorArmengaud, Jean
dc.contributor.authorBessho, Yoshitaka
dc.contributor.authorWetzel, Collin
dc.contributor.authorCao, Xiaoyu
dc.contributor.authorLimbach, Patrick A.
dc.contributor.authorde Crécy-Lagard, Valérie
dc.contributor.authorKoehrer, Caroline
dc.contributor.authorRajbhandary, Uttam L
dc.date.accessioned2016-12-02T20:38:51Z
dc.date.available2016-12-02T20:38:51Z
dc.date.issued2015-09
dc.date.submitted2015-08
dc.identifier.issn0950382X
dc.identifier.urihttp://hdl.handle.net/1721.1/105541
dc.description.abstractThreonylcarbamoyladenosine (t[superscript 6]A) is a modified nucleoside universally conserved in tRNAs in all three kingdoms of life. The recently discovered genes for t6A synthesis, including tsaC and tsaD, are essential in model prokaryotes but not essential in yeast. These genes had been identified as antibacterial targets even before their functions were known. However, the molecular basis for this prokaryotic-specific essentiality has remained a mystery. Here, we show that t[superscript 6]A is a strong positive determinant for aminoacylation of tRNA by bacterial-type but not by eukaryotic-type isoleucyl-tRNA synthetases and might also be a determinant for the essential enzyme tRNA[superscript Ile]-lysidine synthetase. We confirm that t6A is essential in Escherichia coli and a survey of genomewide essentiality studies shows that genes for t[superscrip 6]A synthesis are essential in most prokaryotes. This essentiality phenotype is not universal in Bacteria as t[superscript 6]A is dispensable in Deinococcus radiodurans, Thermus thermophilus, Synechocystis PCC6803 and Streptococcus mutans. Proteomic analysis of t6A- D. radiodurans strains revealed an induction of the proteotoxic stress response and identified genes whose translation is most affected by the absence of t[superscript 6]A in tRNAs. Thus, although t[superscript 6]A is universally conserved in tRNAs, its role in translation might vary greatly between organisms.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01 GM17151)en_US
dc.language.isoen_US
dc.publisherWiley Blackwellen_US
dc.relation.isversionofhttp://dx.doi.org/10.1111/mmi.13209en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleEssentiality of threonylcarbamoyladenosine (t[superscript 6]A), a universal tRNA modification, in bacteriaen_US
dc.title.alternativeEssentiality of threonylcarbamoyladenosine (t6A), a universal tRNA modification, in bacteriaen_US
dc.typeArticleen_US
dc.identifier.citationThiaville, Patrick C. et al. “Essentiality of Threonylcarbamoyladenosine (T 6 A), a Universal tRNA Modification, in Bacteria: T 6 A Essentiality.” Molecular Microbiology 98.6 (2015): 1199–1221.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorKoehrer, Caroline
dc.contributor.mitauthorRajbhandary, Uttam L
dc.relation.journalMolecular Microbiologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsThiaville, Patrick C.; El Yacoubi, Basma; Köhrer, Caroline; Thiaville, Jennifer J.; Deutsch, Chris; Iwata-Reuyl, Dirk; Bacusmo, Jo Marie; Armengaud, Jean; Bessho, Yoshitaka; Wetzel, Collin; Cao, Xiaoyu; Limbach, Patrick A.; RajBhandary, Uttam L.; de Crécy-Lagard, Valérieen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-4530-5647
mit.licenseOPEN_ACCESS_POLICYen_US


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