Data/hora: 11/06/2024 01:29:14

Provedor de dados: | 5
País: | France
Título: | P21-activated kinase 4 (PAK4) is required for metaphase spindle positioning and anchoring
Autores: | Bompard, G.; Rabeharivelo, G.; Cau, J.; Abrieu, A.; Delsert, Claude; Morin, N.
Data: | 2013-02
Ano: | 2013
Palavras-chave: | P21-activated kinase 4; Metaphase; Spindle orientation; Spindle assembly checkpoint.
Resumo: | The oncogenic kinase PAK4 was recently found to be involved in the regulation of the G1 phase and the G2/M transition of the cell cycle. We have also identified that PAK4 regulates Ran GTPase activity during mitosis. Here, we show that after entering mitosis, PAK4-depleted cells maintain a prolonged metaphase-like state. In these cells, chromosome congression to the metaphase plate occurs with normal kinetics but is followed by an extended period during which membrane blebbing and spindle rotation are observed. These bipolar PAK4-depleted metaphase-like spindles have a defective astral microtubule MT network and are not centered in the cell but are in close contact with the cell cortex. As the metaphase-like state persists, centrosome fragmentation occurs, chromosomes scatter from the metaphase plate and move toward the spindle poles with an active spindle assembly checkpoint, a phenotype that is reminiscent of cohesion fatigue. PAK4 also regulates the acto-myosin cytoskeleton and we report that PAK4 depletion results in the induction of cortical membrane blebbing during prometaphase arrest. However, we show that membrane blebs, which are strongly enriched in phospho-cofilin, are not responsible for the poor anchoring of the spindle. As PAK4 depletion interferes with the localization of components of the dynein/dynactin complexes at the kinetochores and on the astral MTs, we propose that loss of PAK4 could induce a change in the activities of motor proteins., Oncogene (2013) 32, 910-919; doi:10.1038/onc.2012.98; published online 26 March 2012
Tipo: | Text
Idioma: | Inglês

Identificador:

http://archimer.ifremer.fr/doc/00133/24465/22502.pdf

DOI:10.1038/onc.2012.98

http://archimer.ifremer.fr/doc/00133/24465/

Editor: | Nature Publishing Group
Formato: | application/pdf
Fonte: | Oncogene (0950-9232) (Nature Publishing Group), 2013-02 , Vol. 32 , N. 7 , P. 910-919

Fonte:

2013, Rights Managed by Nature Publishing Group

info:eu-repo/semantics/openAccess

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