PXD010629 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Identification of CDC20/CDC20B partners in HEK cells demonstrates that CDC20, but not CDC20B, interacts with multiple APC/C components |
Description | Multiciliated cells (MCCs) harbour dozens to hundreds of motile cilia, which beat in a synchronized and directional manner, thus generating hydrodynamic forces important in animal physiology. In vertebrates, MCC differentiation critically depends on the synthesis and release of numerous centrioles by specialized structures called deuterosomes. Little is known about the composition, organization and regulation of deuterosomes. Here, single-cell RNA sequencing reveals that human deuterosome-stage MCCs are characterized by the expression of many cell cycle-related genes. We further investigated the uncharacterized vertebrate specific cell division cycle 20B (CDC20B) gene, the host gene of microRNA-449abc. We show that the CDC20B protein associates to deuterosomes and is required for the release of centrioles and the subsequent production of cilia in mouse and Xenopus MCCs. CDC20B interacts with PLK1, which has been shown to coordinate centriole disengagement with the protease Separase in mitotic cells. Strikingly, over-expression of Separase rescued centriole disengagement and cilia production in CDC20B-deficient MCCs. This work reveals the shaping of a new biological function, deuterosome-mediated centriole production in vertebrate MCCs, by adaptation of canonical and recently evolved cell cycle-related molecules. A specific aim of this mass spectrometry experiment was to verify on immunoprecipitated protein complexes from CDC20 or CDC20B transfected HEK cells that CDC20, but not CDC20B, interacts with multiple APC/C components. |
HostingRepository | PRIDE |
AnnounceDate | 2019-04-03 |
AnnouncementXML | Submission_2019-04-03_02:17:24.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Pascal BARBRY |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | Q Exactive |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2018-07-31 05:56:37 | ID requested | |
⏵ 1 | 2019-04-03 02:17:25 | announced | |
2 | 2024-10-22 04:47:27 | announced | 2024-10-22: Updated project metadata. |
Publication List
Revinski DR, Zaragosi LE, Boutin C, Ruiz-Garcia S, Deprez M, Thom, é V, Rosnet O, Gay AS, Mercey O, Paquet A, Pons N, Ponzio G, Marcet B, Kodjabachian L, Barbry P, CDC20B is required for deuterosome-mediated centriole production in multiciliated cells. Nat Commun, 9(1):4668(2018) [pubmed] |
Keyword List
curator keyword: Biological |
submitter keyword: HEK cells, centriole, deuterosome, motile cilia, CDC20B, Separase, PLK1, CDC20, cell cycle |
Contact List
Pascal Barbry |
contact affiliation | Université Côte d'Azur, CNRS |
contact email | barbry@ipmc.cnrs.fr |
lab head | |
Pascal BARBRY |
contact affiliation | Université Côte d'Azur |
contact email | barbry@ipmc.cnrs.fr |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
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[ - ]
- PRIDE
- PXD010629
- Label: PRIDE project
- Name: Identification of CDC20/CDC20B partners in HEK cells demonstrates that CDC20, but not CDC20B, interacts with multiple APC/C components