{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ni Z"],"funding":["CIHR Postdoctoral Fellowship","Canadian Institutes of Health Research","CIHR"],"pagination":["4483-4501"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11077057"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["52(8)"],"pubmed_abstract":["Messenger RNA precursors (pre-mRNA) generally undergo 3' end processing by cleavage and polyadenylation (CPA), which is specified by a polyadenylation site (PAS) and adjacent RNA sequences and regulated by a large variety of core and auxiliary CPA factors. To date, most of the human CPA factors have been discovered through biochemical and proteomic studies. However, genetic identification of the human CPA factors has been hampered by the lack of a reliable genome-wide screening method. We describe here a dual fluorescence readthrough reporter system with a PAS inserted between two fluorescent reporters. This system enables measurement of the efficiency of 3' end processing in living cells. Using this system in combination with a human genome-wide CRISPR/Cas9 library, we conducted a screen "],"journal":["Nucleic acids research"],"pubmed_title":["Identifying human pre-mRNA cleavage and polyadenylation factors by genome-wide CRISPR screens using a dual fluorescence readthrough reporter."],"pmcid":["PMC11077057"],"funding_grant_id":["FDN-154338"],"pubmed_authors":["Tong AHY","Guo X","Chan K","Greenblatt JF","Ha KCH","Burke GL","Song J","Ahmed N","Marcon E","Ni Z","Moffat J","Blencowe BJ","Nabeel-Shah S","Pu S"],"additional_accession":[]},"is_claimable":false,"name":"Identifying human pre-mRNA cleavage and polyadenylation factors by genome-wide CRISPR screens using a dual fluorescence readthrough reporter.","description":"Messenger RNA precursors (pre-mRNA) generally undergo 3' end processing by cleavage and polyadenylation (CPA), which is specified by a polyadenylation site (PAS) and adjacent RNA sequences and regulated by a large variety of core and auxiliary CPA factors. To date, most of the human CPA factors have been discovered through biochemical and proteomic studies. However, genetic identification of the human CPA factors has been hampered by the lack of a reliable genome-wide screening method. We describe here a dual fluorescence readthrough reporter system with a PAS inserted between two fluorescent reporters. This system enables measurement of the efficiency of 3' end processing in living cells. Using this system in combination with a human genome-wide CRISPR/Cas9 library, we conducted a screen ","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 May","modification":"2026-06-01T23:54:54.806Z","creation":"2026-05-24T03:07:19.714Z"},"accession":"S-EPMC11077057","cross_references":{"pubmed":["38587191"],"doi":["10.1093/nar/gkae240"]}}