PXD036595 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | The mitochondrial protease OMA1 acts as a metabolic safeguard upon nuclear DNA damage |
Description | The metabolic plasticity of mitochondria supports cell development and differentiation and ensures cell survival under stress. The peptidase OMA1 regulates mitochondrial morphology and stress signaling and orchestrates tumorigenesis and cell fate decisions in a cell and tissue-specific manner. Here, we have used unbiased systemic approaches to demonstrate that OMA1-dependent cell fate decisions are under metabolic control. A metabolism-focus CRISPR screen combined with an integrated analysis of human expression data unraveled a protective role of OMA1 against DNA damage. Nucleotide deficiencies induced by chemotherapeutic agents promote the selective, p53-dependent apoptosis of cells lacking OMA1. The protective effect of OMA1 does not depend on OMA1 activation nor on OMA1-mediated OPA1 and DELE1 processing. OMA1-deficient cells have reduced glycolytic capacity and accumulate OXPHOS proteins upon DNA damage. OXPHOS inhibition restores glycolysis and confers resistance against DNA damage. Thus, metabolic cues determine cell fate decisions by OMA1, which sheds new light on the role of OMA1 in cancerogenesis. |
HostingRepository | PRIDE |
AnnounceDate | 2023-11-14 |
AnnouncementXML | Submission_2023-11-14_08:44:42.660.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Hendrik Nolte |
SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: 10090; |
ModificationList | No PTMs are included in the dataset |
Instrument | Orbitrap Exploris 480 |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2022-09-08 07:58:31 | ID requested | |
1 | 2023-04-04 03:55:24 | announced | |
2 | 2023-04-09 15:53:18 | announced | 2023-04-09: Updated project metadata. |
⏵ 3 | 2023-11-14 08:44:43 | announced | 2023-11-14: Updated project metadata. |
Publication List
Rivera-Mej, í, as P, Narbona-P, é, rez Á J, Hasberg L, Kroczek L, Bahat A, Lawo S, Folz-Donahue K, Schumacher AL, Ahola S, Mayer FC, Giavalisco P, Nolte H, Lavandero S, Langer T, The mitochondrial protease OMA1 acts as a metabolic safeguard upon nuclear DNA damage. Cell Rep, 42(4):112332(2023) [pubmed] |
Keyword List
submitter keyword: Mitochondria, DIA, OMA1,MEF |
Contact List
Thomas Langer |
contact affiliation | Max-Planck-Institute for Biology of Ageing Department of Mitochondrial Proteostasis Joseph-Stelzmann-Str. 9b 50931 Cologne |
contact email | tlanger@age.mpg.de |
lab head | |
Hendrik Nolte |
contact affiliation | Max Planck Institute for Biology of Ageing, 50931 Cologne, Germany |
contact email | h.nolte@age.mpg.de |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD036595
- Label: PRIDE project
- Name: The mitochondrial protease OMA1 acts as a metabolic safeguard upon nuclear DNA damage