PXD043650 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Phosphoproteomics identifies targets of Mos-MAPK regulating translation and spindle organization in oocyte meiosis |
| Description | The Mos kinase is a constitutive activator of the ERK/MAPK pathway exclusively expressed during oocyte meiosis, mediating key meiotic functions across animal species. While a few of its downstream effectors have been studied in some detail, molecular targets under the control of Mos-MAPK have not yet been identified systematically. Here, we combined live-cell microscopy of starfish oocytes to characterize the cellular phenotypes caused by Mos-MAPK inhibition with phosphoproteomic analysis of synchronous oocyte populations at critical transitions. This revealed a large set of proteins involved in regulation of translation through the CPE-element binding protein CPEB. Our data indicate cyclin B to be a main target of this regulation driving the second meiotic division. A second large group of phospho-proteins identified are regulators of the actin and microtubule cytoskeleton, with a prominent subset of regulators of centrosomal microtubule nucleation. Indeed, we show that Mos-MAPK inhibition increases the size of microtubule asters and promotes separation of spindle poles in anaphase, turning meiotic spindles mitotic-like. We thus identified core molecular modules downstream of Mos-MAPK controlling meiotic functions essential for haploidization and for the highly asymmetric polar body divisions. These modules are widely conserved, thus our findings will likely have general relevance for reproductive processes across species, including humans, and for understanding disease mechanisms when Mos is expressed erroneously, acting as an oncogene. |
| HostingRepository | PRIDE |
| AnnounceDate | 2025-09-03 |
| AnnouncementXML | Submission_2025-09-03_05:17:30.970.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Olexandr Dybkov |
| SpeciesList | scientific name: Echinoderma sp.; NCBI TaxID: 2040765; |
| ModificationList | monohydroxylated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Exploris 480 |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2023-07-10 09:54:07 | ID requested | |
| ⏵ 1 | 2025-09-03 05:17:31 | announced | |
Publication List
Keyword List
| submitter keyword: Phosphoproteomics, oocyte meiosis |
Contact List
| Henning Urlaub |
| contact affiliation | Research Group Bioanalytical Mass Spectrometry, Max Planck Institute for Multidisciplinary Sciences, Germany; Bioanalytics, Department of Clinical Chemistry, University Medical Center Goettingen, Germany |
| contact email | henning.urlaub@mpinat.mpg.de |
| lab head | |
| Olexandr Dybkov |
| contact affiliation | Max Planck Institute for Multidisciplinary Sciences |
| contact email | odybkov@gwdg.de |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD043650
- Label: PRIDE project
- Name: Phosphoproteomics identifies targets of Mos-MAPK regulating translation and spindle organization in oocyte meiosis