PXD064507 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | A Chemogenetic CRISPR Knock-out Screen Uncovers Synergy Between Ubiquitin Signalling and C16orf72/HAPSTR1 for safeguarding S phase integrity |
| Description | Cell cycle progression is orchestrated by a complex interplay between post-translational modifications (PTMs) controlling activation (phosphorylation) and degradation (ubiquitination) of key cell cycle regulators. To comprehensively identify ubiquitin signalling components critical for cell proliferation, we employed a chemical-genetic CRISPR knock-out screen, exploiting the first-in-class ubiquitin E1 inhibitor TAK-243. Our findings provide a systems view of key protein networks underpinning cell cycle progression. We identified 239 genes, including C16orf72/HAPSTR1, whose ablation rendered cells sensitive to a ubiquitin signalling blockade, and 55 genes that conferred resistance under the same conditions. We reveal broad transcriptional changes accompanied with proteome-wide alterations in the ubiquitin signalling landscape upon loss of HAPSTR1 expression, revealing that HAPSTR1 is involved in homeostasis of cell cycle regulators such as CDK6 and CDC6. Mechanistically, we found that HAPSTR1 orchestrates the timing of the G1/S-transition via RB-E2F1 pathway activation by CDK6. Under diminished ubiquitin signalling, compensatory mechanisms fail to respond to accelerated S phase entry and replication stress upon loss of HAPSTR1, eventually compromising cell cycle integrity. Altogether, we provide a valuable resource on the interplay between the ubiquitin system and cell proliferation and uncover HAPSTR1 as a transcriptional regulator orchestrating the G1/S transition. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-09-04 |
| AnnouncementXML | Submission_2026-09-04_06:15:58.559.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Rayman Tjokrodirijo |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Astral |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2025-06-02 04:41:53 | ID requested | |
| ⏵ 1 | 2026-09-04 06:15:59 | announced | |
Publication List
| Dataset with its publication pending |
Keyword List
| submitter keyword: Cell cycle, HAPSTR1, S phase, CDK6, ubiquitin signalling |
Contact List
| Peter A. van Veelen |
| contact affiliation | Head Proteomics Group, Leiden University Medical Center, Center for Proteomics and Metabolomics, PO Box 9600, Postal zone P1-Q, 2300 RC Leiden, The Netherlands |
| contact email | P.A.van_Veelen@lumc.nl |
| lab head | |
| Rayman Tjokrodirijo |
| contact affiliation | Leiden University Medical Center, Proteomics group |
| contact email | r.t.n.tjokrodirijo@lumc.nl |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD064507
- Label: PRIDE project
- Name: A Chemogenetic CRISPR Knock-out Screen Uncovers Synergy Between Ubiquitin Signalling and C16orf72/HAPSTR1 for safeguarding S phase integrity