CDK11(p58) is required for centriole duplication and Plk4 recruitment to mitotic centrosomes

Autor: Nathalie Franck, Pierre Romé, Régis Giet, Emilie Montembault, Aude Pascal, Jean-Yves Cremet
Přispěvatelé: Institut de Génétique et Développement de Rennes (IGDR), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS), RG and NF are funded by the Agence Nationale de la Recherche (programme Jeune Chercheur) and the Ligue Nationale Contre le Cancer (Equipe Labellise). EM and PR are doctoral fellows of the French Ministry of Research., Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), De Villemeur, Hervé
Jazyk: angličtina
Rok vydání: 2011
Předmět:
PLK4
MESH: Protein Transport
MESH: Gene Expression
Centriole
MESH: Cyclin D3
Cell Biology/Cell Growth and Division
lcsh:Medicine
Gene Expression
Mitosis
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
Biology
Protein Serine-Threonine Kinases
MESH: Centrosome
Cell Biology/Cell Signaling
MESH: Protein-Serine-Threonine Kinases
03 medical and health sciences
0302 clinical medicine
Microtubule
Cell Biology/Cytoskeleton
Gene duplication
Humans
MESH: Protein Binding
Cyclin D3
lcsh:Science
[SDV.BC] Life Sciences [q-bio]/Cellular Biology
030304 developmental biology
Centrioles
Centrosome
0303 health sciences
Multidisciplinary
MESH: Humans
MESH: Centrioles
lcsh:R
MESH: Mitosis
Cell biology
MESH: Hela Cells
Protein Transport
030220 oncology & carcinogenesis
lcsh:Q
Chromatid
Cytokinesis
HeLa Cells
Protein Binding
Research Article
Zdroj: PLoS ONE
PLoS ONE, 2011, 6 (1), pp.e14600. ⟨10.1371/journal.pone.0014600⟩
PLoS ONE, Public Library of Science, 2011, 6 (1), pp.e14600. ⟨10.1371/journal.pone.0014600⟩
PLoS ONE, Vol 6, Iss 1, p e14600 (2011)
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0014600⟩
Popis: International audience; BACKGROUND: CDK11(p58) is a mitotic protein kinase, which has been shown to be required for different mitotic events such as centrosome maturation, chromatid cohesion and cytokinesis. METHODOLOGY/PRINCIPAL FINDINGS: In addition to these previously described roles, our study shows that CDK11(p58) inhibition induces a failure in the centriole duplication process in different human cell lines. We propose that this effect is mediated by the defective centrosomal recruitment of proteins at the onset of mitosis. Indeed, Plk4 protein kinase and the centrosomal protein Cep192, which are key components of the centriole duplication machinery, showed reduced levels at centrosomes of mitotic CDK11-depleted cells. CDK11(p58), which accumulates only in the vicinity of mitotic centrosomes, directly interacts with the centriole-associated protein kinase Plk4 that regulates centriole number in cells. In addition, we show that centriole from CDK11 defective cells are not able to be over duplicated following Plk4 overexpression. CONCLUSION/SIGNIFICANCE: We thus propose that CDK11 is required for centriole duplication by two non-mutually-exclusive mechanisms. On one hand, the observed duplication defect could be caused indirectly by a failure of the centrosome to fully maturate during mitosis. On the other hand, CDK11(p58) could also directly regulate key centriole components such as Plk4 during mitosis to trigger essential mitotic centriole modifications, required for centriole duplication during subsequent interphase.
Databáze: OpenAIRE