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Control of human beta-globin mRNA stability and its impact on beta-thalassemia phenotype

dc.contributor.authorPeixeiro, Isabel
dc.contributor.authorSilva, Ana Luísa
dc.contributor.authorRomão, Luísa
dc.date.accessioned2011-11-30T17:27:23Z
dc.date.available2011-11-30T17:27:23Z
dc.date.issued2011-02-28
dc.description.abstractMessenger RNA (mRNA) stability is a critical determinant that affects gene expression. Many pathways have evolved to modulate mRNA stability in response to developmental, physiological and/or environmental stimuli. Eukaryotic mRNAs have a considerable range of half-lives, from as short as a few minutes to as long as several days. Human globin mRNAs constitute an example of highly stable mRNAs. However, a wide variety of naturally occurring mutations that result in the clinical syndrome of thalassemia can trigger accelerated mRNA decay thus controlling mRNA quality prior to translation. Distinct surveillance mechanisms have been described as being targeted for specific defective globin mRNAs. Here, we review mRNA stability mechanisms implicated in the control of beta-globin gene expression and the surveillance pathways that prevent translation of aberrant beta-globin mRNAs. In addition, we emphasize the importance of these pathways in modulating the severity of the beta-thalassemia phenotype.por
dc.identifier.citationHaematologica. 2011 Jun;96(6):905-13. Epub 2011 Feb 28.por
dc.identifier.issn0390-6078
dc.identifier.urihttp://hdl.handle.net/10400.18/333
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherFerrata Storti Foundationpor
dc.relation.publisherversionhttp://www.haematologica.org/content/96/6/905.longpor
dc.subjectmRNA quality controlpor
dc.subjectNonsense-mediated mRNA decaypor
dc.subjectmRNA stabilitypor
dc.subjectBeta-globinpor
dc.subjectBeta-thalassemiapor
dc.subjectClinical phenotypepor
dc.subjectDoenças genéticaspor
dc.titleControl of human beta-globin mRNA stability and its impact on beta-thalassemia phenotypepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage913por
oaire.citation.startPage905por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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