<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Kolakada D</submitter><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Nonsense-mediated mRNA decay (NMD) is a network of pathways that degrades transcripts that undergo premature translation termination. In mammals, NMD can be divided into the exon junction complex (EJC)-enhanced and EJC-independent branches. Fluorescence- and luminescence-based reporters have long been effective tools to investigate NMD, yet existing reporters largely focus on the EJC-enhanced pathway. Here, we present a system of reporters for comparative studies of EJC-independent and EJC-enhanced NMD. This system also enables the study of NMD-associated outcomes such as premature termination codon (PTC) readthrough and truncated protein degradation. These reporters are compatible with fluorescence or luminescence-based readouts via transient transfection or stable integration. Using this</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2023.11.14.567061</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10680754</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A system of reporters for comparative investigation of EJC-independent and EJC-enhanced nonsense-mediated mRNA decay.</pubmed_title><pmcid>PMC10680754</pmcid><funding_grant_id>P30 CA046934</funding_grant_id><funding_grant_id>R35 GM133433</funding_grant_id><funding_grant_id>T32 GM136444</funding_grant_id><pubmed_authors>Lore M</pubmed_authors><pubmed_authors>Jagannathan S</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Campbell AE</pubmed_authors><pubmed_authors>Kolakada D</pubmed_authors><pubmed_authors>Baquero Galvis L</pubmed_authors></additional><is_claimable>false</is_claimable><name>A system of reporters for comparative investigation of EJC-independent and EJC-enhanced nonsense-mediated mRNA decay.</name><description>Nonsense-mediated mRNA decay (NMD) is a network of pathways that degrades transcripts that undergo premature translation termination. In mammals, NMD can be divided into the exon junction complex (EJC)-enhanced and EJC-independent branches. Fluorescence- and luminescence-based reporters have long been effective tools to investigate NMD, yet existing reporters largely focus on the EJC-enhanced pathway. Here, we present a system of reporters for comparative studies of EJC-independent and EJC-enhanced NMD. This system also enables the study of NMD-associated outcomes such as premature termination codon (PTC) readthrough and truncated protein degradation. These reporters are compatible with fluorescence or luminescence-based readouts via transient transfection or stable integration. Using this</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2026-06-22T03:19:26.671Z</modification><creation>2024-10-18T18:16:05.358Z</creation></dates><accession>S-EPMC10680754</accession><cross_references><pubmed>38014198</pubmed><doi>10.1101/2023.11.14.567061</doi></cross_references></HashMap>