Publication
The expression of UPF1 is regulated by a cap-independent translation initiation mechanism and a cryptic promoter within its 5’ untranslated region
| dc.contributor.author | Lacerda, Rafaela | |
| dc.contributor.author | Marques-Ramos, Ana | |
| dc.contributor.author | Teixeira, Alexandre | |
| dc.contributor.author | Romão, Luísa | |
| dc.date.accessioned | 2015-01-29T15:40:13Z | |
| dc.date.available | 2015-01-29T15:40:13Z | |
| dc.date.issued | 2014-11-20 | |
| dc.description.abstract | Regulation of gene expression occurs at several steps, including translation initiation. Under normal circumstances, translation initiation is mainly cap-dependent; however, several proteins can initiate translation in a cap-independent way, allowing the maintenance of these proteins under conditions that reduce global protein synthesis. hUPF1(human up-frameshift 1) plays important roles in several key cellular processes such as nonsense-mediated decay, telomere replication and homeostasis, and cell cycle progression, suggesting its expression must be tightly regulated to prevent abnormal cell proliferation. This protein is essential in the G2/M transition, a step known by a reduced overall protein synthesis. Taking these data into account, we hypothesized that UPF1 might initiate translation in a cap-independent way, allowing the cell to maintain its levels under conditions that impair cap-dependent translation initiation. To test this hypothesis, we cloned the hUPF1 5’UTR in a dicistronic vector and transfected CC and CRC cell lines with either this construct or the control counterparts. We observed a 15- to 25-fold increase in relative luciferase activity of the UPF1 5’UTR-containing construct compared to the levels obtained from the empty counterpart in all tested cell lines, suggesting a cap-independent translation initiation. To control whether luciferase activity levels are due to a cryptic promoter within UPF1 5’UTR, we transfected cells with promoterless plasmids and observed the same result, demonstrating that UPF1 5’UTR contains a cryptic promoter. Transfecting cells with in vitro transcribed mRNAs resulted in a 2-fold increase in protein levels, suggesting that translation can occur in a cap-independent way. This is maintained under conditions of global protein synthesis inhibition. Deletional analysis of UPF1 5’UTR revealed that the first 50 nucleotides are essential for cryptic promoter and cap-independent activities. These results provide new insights on the mechanisms that govern UPF1 expression. | por |
| dc.identifier.uri | http://hdl.handle.net/10400.18/2714 | |
| dc.language.iso | eng | por |
| dc.peerreviewed | yes | por |
| dc.subject | Genómica Funcional | por |
| dc.subject | Genómica Funcional e Estrutural | por |
| dc.subject | Internal Ribosome Entry Site (IRES) | por |
| dc.subject | Nonsense-mediated mRNA Decay (NMD) | por |
| dc.subject | mRNA Translation | por |
| dc.title | The expression of UPF1 is regulated by a cap-independent translation initiation mechanism and a cryptic promoter within its 5’ untranslated region | por |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.citation.conferencePlace | Lisboa, Portugal | por |
| oaire.citation.title | 18ª Reunião Anual da Sociedade Portuguesa de Genética Humana, 19-21 novembro 2014 | por |
| rcaap.rights | openAccess | por |
| rcaap.type | conferenceObject | por |