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Translational regulation of the human PERK by upstream open reading frames

datacite.subject.fosCiências Médicas::Ciências da Saúde
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorSilvestre, Samuel
dc.date.accessioned2026-03-09T15:34:45Z
dc.date.available2026-03-09T15:34:45Z
dc.date.issued2025-11-05
dc.description.abstractUpstream open reading frames (uORFs) are cis-acting elements located within the 5’ leader sequence (5’UTR) of transcripts, which can regulate protein synthesis, i.e. mRNA translation, of the correspondent main open reading frame (mORF). During endoplasmic reticulum (ER) stress, the accumulation of unfolded proteins activates the ER-resident PKR-like ER kinase (PERK), which results in phosphorylation of eIF2α to inhibit global mRNA translation, while allowing the selective uORF-mediated translation of downstream effectors responsible for stress resolution or, ultimately, cell death. The dual role of PERK in regulating cell fate was implicated in human diseases, like diabetes, neurodegenerative disorders and cancer. Moreover, mutations in the EIF2AK3 gene (encoding PERK) were associated with the rare genetic disease, Wolcott-Rallison Syndrome (WRS). In this work, we aimed to study the translational regulatory role of 5 AUG- and 3 non-AUG-uORFs identified in the PERK 5’UTR and assess its biological relevance. Altogether, we highlight the importance of including 5’UTRs in the screening of disease-related mutations and the necessity of functional studies to assess their role in pathogenesis.eng
dc.identifier.urihttp://hdl.handle.net/10400.18/11249
dc.language.isopor
dc.peerreviewedn/a
dc.rights.uriN/A
dc.subjectPERK
dc.subjectTranslational Control
dc.subjectIntegrated Stress Response (ISR)
dc.subjectuORFs
dc.subjectGenómica Funcional e Estrutural
dc.titleTranslational regulation of the human PERK by upstream open reading frameseng
dc.typelearning object
dspace.entity.typePublication
oaire.citation.titleSeminário DGH, INSA, 5 novembro 2025
oaire.versionhttp://purl.org/coar/version/c_b1a7d7d4d402bcce

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