{"doi":"10.1101/2021.01.27.428318","title":"An alternative UPF1 isoform drives conditional remodeling of nonsense-mediated mRNA decay","abstract":"Abstract The nonsense-mediated mRNA decay (NMD) pathway monitors translation termination to degrade transcripts with premature stop codons and regulate thousands of human genes. Here we show that an alternative mammalian-specific isoform of the core NMD factor UPF1, termed UPF1 LL , enables condition-dependent remodeling of NMD specificity. Previous studies indicate that the extension of a conserved regulatory loop in the UPF1 LL helicase core confers a decreased propensity to dissociate from RNA upon ATP hydrolysis relative to the major UPF1 isoform, designated UPF1 SL . Using biochemical and transcriptome-wide approaches, we find that UPF1 LL overcomes the protective RNA binding proteins PTBP1 and hnRNP L to preferentially bind and down-regulate long 3’UTRs normally shielded from NMD. Unexpectedly, UPF1 LL supports induction of NMD on new populations of substrate mRNAs in response to activation of the integrated stress response and impaired translation efficiency. Thus, while canonical NMD is abolished by moderate translational repression, UPF1 LL activity is enhanced, providing a mechanism to rapidly rewire NMD specificity in response to cellular stress.","journal":"bioRxiv (Cold Spring Harbor Laboratory)","year":2021,"id":220134,"datarank":0.0,"base_score":0.0,"endowment":0.0,"self_citation_contribution":0.0,"citation_network_contribution":0.0,"self_endowment_contribution":0.0,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":1,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9486,"is_data_producer":false,"deposit_databanks":null,"is_oa":true,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2021-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":348287,"name":"Soumya Ranganathan","orcid":"0000-0002-5655-223X","position":1,"is_corresponding":false},{"id":348288,"name":"Clara D. Wang","orcid":"0000-0002-7522-1719","position":2,"is_corresponding":false},{"id":348289,"name":"J. Robert Hogg","orcid":"0000-0001-5729-5135","position":3,"is_corresponding":false},{"id":348286,"name":"Sarah E. Fritz","orcid":"0000-0001-6318-4319","position":0,"is_corresponding":true}],"reference_count":95,"raw_metadata":null,"created_at":"2026-07-18T23:53:42.928212Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}