Role of the protein kinase Kin1 and nuclear centering in actomyosin ring formation in fission yeast

Autor: Cathy Le Goff, Anne Couturier, Xavier Le Goff, Stéphanie La Carbona, Angela Cadou
Přispěvatelé: De Villemeur, Hervé, Institut de Génétique et Développement de Rennes (IGDR), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS), Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2009
Předmět:
MESH: Cytokinesis
Cell division
Down-Regulation
cytokinesis
MESH: Actomyosin
Polo-like kinase
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
Biology
Protein Serine-Threonine Kinases
Septin
Article
MESH: Down-Regulation
MESH: Protein-Serine-Threonine Kinases
Pom1
03 medical and health sciences
Schizosaccharomyces
Molecular Biology
Mitosis
[SDV.BC] Life Sciences [q-bio]/Cellular Biology
MESH: Protein Kinases
Alleles
ComputingMilieux_MISCELLANEOUS
030304 developmental biology
mitosis
0303 health sciences
MESH: Alleles
030302 biochemistry & molecular biology
cytoskeleton
MESH: Schizosaccharomyces pombe Proteins
Cell Biology
Actomyosin
Cell cycle
Cell biology
contractile actomyosin ring
cell polarity
MESH: Microtubule-Associated Proteins
MESH: Schizosaccharomyces
Schizosaccharomyces pombe
Interphase
cell cycle
Schizosaccharomyces pombe Proteins
Microtubule-Associated Proteins
Protein Kinases
Cytokinesis
Developmental Biology
Zdroj: Cell Cycle
Cell Cycle, 2009, 8 (15), pp.2451-62. ⟨10.4161/cc.8.15.9219⟩
Cell Cycle, Taylor & Francis, 2009, 8 (15), pp.2451-62. ⟨10.4161/cc.8.15.9219⟩
ISSN: 1538-4101
1551-4005
DOI: 10.4161/cc.8.15.9219⟩
Popis: Cytokinesis is the last step of the cell cycle, producing two daughter cells inheriting equal genetic information. This process involves the assembly of an actomyosin ring during mitosis. In the fission yeast Schizosaccharomyces pombe, cytokinesis occurs at the geometric cell centre, a position which is defined by the interphase nucleus and the anilin-related Mid1 protein. The pom1Delta, tea1Delta and tea4Delta mutants are defective in restricting Mid1 as a band around the nucleus and misplace the division site. We previously reported that inhibition of the protein kinase Kin1 promoted failure of cytokinesis in pom1Delta and tea1Delta cells but the mechanism involving Kin1 remained elusive. Here we investigated the contribution of Kin1 in cytokinesis. We show that Kin1-GFP has a dynamic cell cycle regulated distribution. Like pom1Delta and tea1Delta, tea4Delta exhibits a strong genetic interaction with kin1Delta. Using a conditional repressible kin1 allele that only alters interphase nuclear centering, we observed that Kin1 downregulation severely compromised actomyosin ring formation and septum synthesis in tea4Delta cells. In addition, nuclear displacement induced either by overexpression of a putative catalytically inactive Kin1 mutant, by chemically mediated microtubule depolymerization or by mutation in the par1Delta gene impaired cytokinesis in tea4Delta but not tea4(+) cells. We propose that nuclear mispositioning exacerbates the tea4Delta, pom1Delta and tea1Delta cell division phenotype. Our work reveal that nuclear centering becomes essential when Pom1/Tea1/Tea4 function is compromised and that Kin1 expression level is a key regulatory element in this situation. Our results suggest the existence of distinct overlapping control mechanisms to ensure efficient cell division.
Databáze: OpenAIRE