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dc.contributor.author | Moreira, Ricardo N | |
dc.contributor.author | Domingues, Susana | |
dc.contributor.author | Viegas, Sandra C | |
dc.contributor.author | Amblar, Monica | |
dc.contributor.author | Arraiano, Cecília M | |
dc.date.accessioned | 2019-02-28T12:20:19Z | |
dc.date.available | 2019-02-28T12:20:19Z | |
dc.date.issued | 2012-11-20 | |
dc.identifier.citation | BMC Microbiol. 2012 Nov 20;12:268. | es_ES |
dc.identifier.issn | 1471-2180 | es_ES |
dc.identifier.uri | http://hdl.handle.net/20.500.12105/7256 | |
dc.description.abstract | BACKGROUND: Ribonuclease R (RNase R) is an exoribonuclease that recognizes and degrades a wide range of RNA molecules. It is a stress-induced protein shown to be important for the establishment of virulence in several pathogenic bacteria. RNase R has also been implicated in the trans-translation process. Transfer-messenger RNA (tmRNA/SsrA RNA) and SmpB are the main effectors of trans-translation, an RNA and protein quality control system that resolves challenges associated with stalled ribosomes on non-stop mRNAs. Trans-translation has also been associated with deficiencies in stress-response mechanisms and pathogenicity. RESULTS: In this work we study the expression of RNase R in the human pathogen Streptococcus pneumoniae and analyse the interplay of this enzyme with the main components of the trans-translation machinery (SmpB and tmRNA/SsrA). We show that RNase R is induced after a 37°C to 15°C temperature downshift and that its levels are dependent on SmpB. On the other hand, our results revealed a strong accumulation of the smpB transcript in the absence of RNase R at 15°C. Transcriptional analysis of the S. pneumoniae rnr gene demonstrated that it is co-transcribed with the flanking genes, secG and smpB. Transcription of these genes is driven from a promoter upstream of secG and the transcript is processed to yield mature independent mRNAs. This genetic organization seems to be a common feature of Gram positive bacteria, and the biological significance of this gene cluster is further discussed. CONCLUSIONS: This study unravels an additional contribution of RNase R to the trans-translation system by demonstrating that smpB is regulated by this exoribonuclease. RNase R in turn, is shown to be under the control of SmpB. These proteins are therefore mutually dependent and cross-regulated. The data presented here shed light on the interactions between RNase R, trans-translation and cold-shock response in an important human pathogen. | es_ES |
dc.description.sponsorship | This work was supported by several grants from FCT, including grant PEst-OE/EQB/LA0004/2011 and the work at Instituto de Salud Carlos III was supported by Fondo de Investigación Sanitaria (FIS) (PI08/0442 and PI11/00656), CIBER Enfermedades Respiratorias (initiative of the Instituto de Salud Carlos III) in Spain, and by the Bilateral Collaboration program between Conselho Reitores Universidades Portuguesas (CRUP) from Portugal and Ministerio de Ciencia e Innovación (MICINN) (HP2008-0041) Acciones Integradas of Spain. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | BioMed Central (BMC) | es_ES |
dc.type.hasVersion | VoR | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject.mesh | Exoribonucleases | es_ES |
dc.subject.mesh | RNA-Binding Proteins | es_ES |
dc.subject.mesh | Streptococcus pneumoniae | es_ES |
dc.subject.mesh | Temperature | es_ES |
dc.subject.mesh | Gene Expression Regulation, Bacterial | es_ES |
dc.subject.mesh | Protein Biosynthesis | es_ES |
dc.subject.mesh | RNA Stability | es_ES |
dc.subject.mesh | Transcription, Genetic | es_ES |
dc.title | Synergies between RNA degradation and trans-translation in Streptococcus pneumoniae: cross regulation and co-transcription of RNase R and SmpB | es_ES |
dc.type | journal article | es_ES |
dc.rights.license | Atribución 4.0 Internacional | * |
dc.identifier.pubmedID | 23167513 | es_ES |
dc.format.volume | 12 | es_ES |
dc.format.number | 1 | es_ES |
dc.format.page | 268 | es_ES |
dc.identifier.doi | 10.1186/1471-2180-12-268 | es_ES |
dc.contributor.funder | Instituto de Salud Carlos III | |
dc.contributor.funder | Ministerio de Ciencia e Innovación (España) | |
dc.contributor.funder | Conselho Reitores Universidades Portuguesas | |
dc.description.peerreviewed | Sí | es_ES |
dc.relation.publisherversion | https://doi.org/10.1186/1471-2180-12-268 | es_ES |
dc.identifier.journal | BMC microbiology | es_ES |
dc.repisalud.centro | ISCIII::Centro Nacional de Microbiología | es_ES |
dc.repisalud.institucion | ISCIII | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/ES/PI08/0442 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/ES/PI11/00656 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/ES/HP2008-0041 | es_ES |
dc.rights.accessRights | open access | es_ES |