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dc.contributor.authorMateus, Denisa D.pt_PT
dc.contributor.authorParedes, João A.pt_PT
dc.contributor.authorEspañol, Yaizapt_PT
dc.contributor.authorRibas de Pouplana, Lluíspt_PT
dc.contributor.authorMoura, Gabriela R.pt_PT
dc.contributor.authorSantos, Manuel A. S.pt_PT
dc.date.accessioned2018-10-11T14:31:41Z-
dc.date.available2018-10-11T14:31:41Z-
dc.date.issued2013-
dc.identifier.issn1547-6286pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/24276-
dc.description.abstractFungi of the CTG clade translate the Leu CUG codon as Ser. This genetic code alteration is the only eukaryotic sense-to-sense codon reassignment known to date, is mediated by an ambiguous serine tRNA (tRNACAG(Ser)), exposes unanticipated flexibility of the genetic code and raises major questions about its selection and fixation in this fungal lineage. In particular, the origin of the tRNACAG(Ser) and the evolutionary mechanism of CUG reassignment from Leu to Ser remain poorly understood. In this study, we have traced the origin of the tDNACAG(Ser) gene and studied critical mutations in the tRNACAG(Ser) anticodon-loop that modulated CUG reassignment. Our data show that the tRNACAG(Ser) emerged from insertion of an adenosine in the middle position of the 5'-CGA-3'anticodon of a tRNACGA(Ser) ancestor, producing the 5'-CAG-3' anticodon of the tRNACAG(Ser), without altering its aminoacylation properties. This mutation initiated CUG reassignment while two additional mutations in the anticodon-loop resolved a structural conflict produced by incorporation of the Leu 5'-CAG-3'anticodon in the anticodon-arm of a tRNA(Ser). Expression of the mutant tRNACAG(Ser) in yeast showed that it cannot be expressed at physiological levels and we postulate that such downregulation was essential to maintain Ser misincorporation at sub-lethal levels during the initial stages of CUG reassignment. We demonstrate here that such low level CUG ambiguity is advantageous in specific ecological niches and we propose that misreading tRNAs are targeted for degradation by an unidentified tRNA quality control pathway.pt_PT
dc.description.sponsorshipD.D.M. was financially supported by FCT (PhD grant SFRH/BD/2006/27867). We thank Rita Rocha for her help with SerRS purification. This study was funded by FEDER/ FCT projects PTDC/BIA-MIC/099826/2008 and PTDC/ BIA-GEN/110383/2009.pt_PT
dc.language.isoengpt_PT
dc.publisherTaylor & Francispt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/99826/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/110383/PTpt_PT
dc.rightsrestrictedAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectCTG cladept_PT
dc.subjectCUG codonpt_PT
dc.subjectCandida albicanspt_PT
dc.subjectevolutionpt_PT
dc.subjectgenetic codept_PT
dc.subjecttRNApt_PT
dc.titleMolecular reconstruction of a fungal genetic code alterationpt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage969pt_PT
degois.publication.issue6pt_PT
degois.publication.lastPage980pt_PT
degois.publication.titleRNA Biologypt_PT
degois.publication.volume10pt_PT
dc.identifier.doi10.4161/rna.24683pt_PT
dc.identifier.essn1555-8584pt_PT
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