{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Pesiridis GS"],"funding":["NIA NIH HHS"],"pagination":["18845-55"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3099701"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["286(21)"],"pubmed_abstract":["Carboxyl-terminal fragments (CTFs) of TDP-43 aggregate to form the diagnostic signature inclusions of frontotemporal lobar degeneration and amyotrophic lateral sclerosis, but the biological significance of these CTFs and how they are generated remain enigmatic. To address these issues, we engineered mammalian cells with an inducible tobacco etch virus (TEV) protease that cleaves TDP-43 containing a TEV cleavage site. Regions of TDP-43 flanking the second RNA recognition motif (RRM2) are efficiently cleaved by TEV, whereas sites within this domain are more resistant to cleavage. CTFs containing RRM2 generated from de novo cleavage of nuclear TDP-43 are transported to the cytoplasm and efficiently cleared, indicating that cleavage alone is not sufficient to initiate CTF aggregation. However,"],"journal":["The Journal of biological chemistry"],"pubmed_title":["A \"two-hit\" hypothesis for inclusion formation by carboxyl-terminal fragments of TDP-43 protein linked to RNA depletion and impaired microtubule-dependent transport."],"pmcid":["PMC3099701"],"funding_grant_id":["AG17586","P01 AG017586"],"pubmed_authors":["Pesiridis GS","Tripathy K","Lee VM","Tanik S","Trojanowski JQ"],"additional_accession":[]},"is_claimable":false,"name":"A \"two-hit\" hypothesis for inclusion formation by carboxyl-terminal fragments of TDP-43 protein linked to RNA depletion and impaired microtubule-dependent transport.","description":"Carboxyl-terminal fragments (CTFs) of TDP-43 aggregate to form the diagnostic signature inclusions of frontotemporal lobar degeneration and amyotrophic lateral sclerosis, but the biological significance of these CTFs and how they are generated remain enigmatic. To address these issues, we engineered mammalian cells with an inducible tobacco etch virus (TEV) protease that cleaves TDP-43 containing a TEV cleavage site. Regions of TDP-43 flanking the second RNA recognition motif (RRM2) are efficiently cleaved by TEV, whereas sites within this domain are more resistant to cleavage. CTFs containing RRM2 generated from de novo cleavage of nuclear TDP-43 are transported to the cytoplasm and efficiently cleared, indicating that cleavage alone is not sufficient to initiate CTF aggregation. However,","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011 May","modification":"2026-05-03T16:57:55.782Z","creation":"2026-04-07T19:25:21.365Z"},"accession":"S-EPMC3099701","cross_references":{"pubmed":["21454607"],"doi":["10.1074/jbc.m111.231118","10.1074/jbc.M111.231118"]}}