PXD017239 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | TEX264 coordinates p97- and SPRTN-mediated resolution of topoisomerase 1-DNA adducts |
Description | Eukaryotic topoisomerase 1 (TOP1) regulates DNA topology to ensure efficient DNA replication and transcription. TOP1 is also a major driver of endogenous genome instability, particularly when its catalytic intermediate - a covalent TOP1-DNA adduct known as a TOP1 cleavage complex (TOP1cc) - is stabilised. TOP1ccs are highly cytotoxic and a failure to resolve them underlies the pathology of neurological disorders but is also exploited in cancer therapy where TOP1ccs are the target of widely used frontline anti-cancer drugs. A critical enzyme for TOP1cc resolution is the tyrosyl-DNA phosphodiesterase, TDP1, which hydrolyses the bond that links a tyrosine in the active site of TOP1 to a 3’ phosphate group on a single-stranded (ss)DNA break. However, TDP1 can only process small peptide fragments from ssDNA ends, raising the question of how the ~90 kDa TOP1 protein is processed upstream of TDP1. We find that TEX264 fulfils this role by forming a complex with the p97 ATPase and the SPRTN metalloprotease. We show that TEX264 recognises both unmodified and SUMO1-modifed TOP1 and initiates TOP1cc repair by recruiting p97 and SPRTN. TEX264 localises to the nuclear periphery, associates with DNA replication forks, and counteracts TOP1ccs during DNA replication. Altogether, our study elucidates the existence of a specialised repair complex required for upstream proteolysis of TOP1ccs and their subsequent resolution. |
HostingRepository | PRIDE |
AnnounceDate | 2024-10-07 |
AnnouncementXML | Submission_2024-10-07_10:35:19.390.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD017239 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | iolanda Vendrell |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | Oxidation; Acetyl; Carbamidomethyl |
Instrument | Orbitrap Fusion Lumos; LTQ Orbitrap Velos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2020-01-21 08:24:08 | ID requested | |
⏵ 1 | 2024-10-07 10:35:20 | announced | |
Publication List
10.1038/s41467-020-15000-w; |
10.6019/PXD017239; |
Fielden J, Wiseman K, Torrecilla I, Li S, Hume S, Chiang SC, Ruggiano A, Narayan Singh A, Freire R, Hassanieh S, Domingo E, Vendrell I, Fischer R, Kessler BM, Maughan TS, El-Khamisy SF, Ramadan K, TEX264 coordinates p97- and SPRTN-mediated resolution of topoisomerase 1-DNA adducts. Nat Commun, 11(1):1274(2020) [pubmed] |
Keyword List
submitter keyword: protein-DNA adducts, VCP/p97, TOP1, TEX264,DNA repair, genome stability, SPRTN, DNA replication |
Contact List
Kristijan Ramadan |
contact affiliation | Cancer Research UK and Medical Research Council Oxford Institute for Radiation Oncology, Department of Oncology, University of Oxford, Oxford, OX3 7DQ, UK |
contact email | kristijan.ramadan@oncology.ox.ac.uk |
lab head | |
iolanda Vendrell |
contact affiliation | CRUK-MRC Oxford Institute for Radiation Oncology, Oxford University |
contact email | iolanda.vendrell@oncology.ox.ac.uk |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD017239
- Label: PRIDE project
- Name: TEX264 coordinates p97- and SPRTN-mediated resolution of topoisomerase 1-DNA adducts