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UNC-45A is required for neurite extension via controlling NMII activation

UNC-45A is a highly conserved member of the UNC-45/CRO1/She4p family of proteins, which act as chaperones for conventional and nonconventional myosins. NMII mediates contractility and actin-based motility, which are fundamental for proper growth cone motility and neurite extension. The presence and...

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Detalles Bibliográficos
Autores principales: Iizuka, Yoshie, Mooneyham, Ashley, Sieben, Andrew, Chen, Kevin, Maile, Makayla, Hellweg, Raffaele, Schütz, Florian, Teckle, Kebebush, Starr, Timothy, Thayanithy, Venugopal, Vogel, Rachel Isaksson, Lou, Emil, Lee, Michael K., Bazzaro, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426848/
https://www.ncbi.nlm.nih.gov/pubmed/28356421
http://dx.doi.org/10.1091/mbc.E16-06-0381
Descripción
Sumario:UNC-45A is a highly conserved member of the UNC-45/CRO1/She4p family of proteins, which act as chaperones for conventional and nonconventional myosins. NMII mediates contractility and actin-based motility, which are fundamental for proper growth cone motility and neurite extension. The presence and role of UNC-45A in neuronal differentiation have been largely unknown. Here we demonstrate that UNC-45A is a novel growth cone–­localized, NMII-associated component of the multiprotein complex regulating growth cone dynamics. We show that UNC-45A is dispensable for neuron survival but required for neurite elongation. Mechanistically, loss of UNC-45A results in increased levels of NMII activation. Collectively our results provide novel insights into the molecular mechanisms of neurite growth and define UNC-45A as a novel and master regulator of NMII-mediated cellular processes in neurons.