Publicação
Dissecting the DIS3L2 target-specificity of transcripts committed to nonsense-mediated decay in human cells
| datacite.subject.fos | Ciências Médicas | |
| datacite.subject.sdg | 03:Saúde de Qualidade | |
| dc.contributor.author | Garcia-Moreno, Juan F. | |
| dc.contributor.author | Carvalho, Miguel P. | |
| dc.contributor.author | Lacerda, Rafaela | |
| dc.contributor.author | Romão, Luísa | |
| dc.date.accessioned | 2026-02-05T11:23:35Z | |
| dc.date.available | 2026-02-05T11:23:35Z | |
| dc.date.issued | 2025-06-05 | |
| dc.description.abstract | Nonsense-mediated mRNA decay (NMD) is a conserved surveillance mechanism that eliminates mRNAs harboring premature termination codons (PTCs) and regulates the expression of certain physiological transcripts. The 3’-to-5’ exoribonuclease DIS3L2 degrades different RNAs independently of the RNA exosome, following uridylation at the 3' end by the terminal uridylyl transferases TUT4 and TUT7. We and others have shown that DIS3L2 is involved in NMD in an uridylation-dependent manner, being its function in NMD target-specific (Kurosaki et al. 2018; da Costa et al. 2019). Now, we aim to characterize the mechanisms involved in DIS3L2/NMD-target specificity. We used our RNA-seq data already obtained and validated and compared the transcripts upregulated upon DIS3L2 knockdown (REF) with a validated NMD-target set (Colombo et al., 2017). We observed that about 7% of DIS3L2-sensitive transcripts overlap with known NMD-targets. Considering the different groups of transcripts, we then analyzed specific features that make some NMD-targets sensitive to DIS3L2 (so called DIS3L2/NMD-targets; group 1), versus the remaining NMD-targets (DIS3L2-resistant NMD-targets; group 2), the remaining DIS3L2-sensitive targets (group 3), or the remaining transcriptome (DIS3L2-resistant NMD-targets plus NMD-resistant transcriptome; group 4). We assessed the following genomic features: 5’ and 3’ untranslated region (UTR) lengths, 3’UTR GC-, AU-, G-, C-, A-, and U-contents, presence of 5’UTR upstream open reading frames (uORFs), and 3’UTR introns. Elevated G-, C-, and GC-contents in the 3’UTRs were the most consistent features distinguishing DIS3L2/NMD-targets from the group 4. Comparison between group 1 and 2, and 1 and 3 was not significant. To better characterize the importance of each transcript portion, we are also analyzing hybrid constructs combining regions of the DIS3L2/NMD-resistant human β-globin (HBB) gene and the DIS3L2/NMD-sensitive GADD45A gene expressed in DIS3L2 depleted cultured cells. | eng |
| dc.description.sponsorship | This work was supported by Fundação para a Ciência e Tecnologia, Instituto Nacional de Saúde Doutor Ricardo Jorge and Biosystems and Integrative Sciences Institute (BioISI). | |
| dc.identifier.uri | http://hdl.handle.net/10400.18/10813 | |
| dc.language.iso | eng | |
| dc.peerreviewed | yes | |
| dc.rights.uri | N/A | |
| dc.subject | Nonsense-mediated mRNA Decay (NMD) | |
| dc.subject | DIS3L2 | |
| dc.subject | Uridylation | |
| dc.subject | Transcript Specificity | |
| dc.subject | 3′UTR GC Content | |
| dc.subject | Genómica Funcional | |
| dc.subject | Genómica Funcional e Estrutural | |
| dc.title | Dissecting the DIS3L2 target-specificity of transcripts committed to nonsense-mediated decay in human cells | eng |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.citation.conferenceDate | 2025-06-05 | |
| oaire.citation.conferencePlace | Oeiras, Portugal | |
| oaire.citation.title | VI International Conference of the Portuguese Society of Genetics, 5-6 June 2025 | |
| oaire.version | http://purl.org/coar/version/c_b1a7d7d4d402bcce |