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Activator-inhibitor coupling between Rho signaling and actin assembly make the cell cortex an excitable medium

Animal cell cytokinesis results from patterned activation of the small GTPase Rho, which directs assembly of actomyosin in the equatorial cortex. Cytokinesis is restricted to a portion of the cell cycle following anaphase onset in which the cortex is responsive to signals from the spindle. We show t...

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Detalles Bibliográficos
Autores principales: Bement, William M., Leda, Marcin, Moe, Alison M., Kita, Angela M., Larson, Matthew E., Golding, Adriana E., Pfeuti, Courtney, Su, Kuan-Chung, Miller, Ann L., Goryachev, Andrew B., von Dassow, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849138/
https://www.ncbi.nlm.nih.gov/pubmed/26479320
http://dx.doi.org/10.1038/ncb3251
Descripción
Sumario:Animal cell cytokinesis results from patterned activation of the small GTPase Rho, which directs assembly of actomyosin in the equatorial cortex. Cytokinesis is restricted to a portion of the cell cycle following anaphase onset in which the cortex is responsive to signals from the spindle. We show that shortly after anaphase onset oocytes and embryonic cells of frogs and echinoderms exhibit cortical waves of Rho activity and F-actin polymerization. The waves are modulated by cyclin-dependent kinase 1 (Cdk1) activity and require the Rho GEF (guanine nucleotide exchange factor), Ect2. Surprisingly, during wave propagation, while Rho activity elicits F-actin assembly, F-actin subsequently inactivates Rho. Experimental and modeling results show that waves represent excitable dynamics of a reaction diffusion system with Rho as the activator and F-actin the inhibitor. We propose that cortical excitability explains fundamental features of cytokinesis including its cell cycle regulation.