Artigo Acesso aberto Revisado por pares

Aurora A phosphorylation of TACC3/maskin is required for centrosome-dependent microtubule assembly in mitosis

2005; Rockefeller University Press; Volume: 170; Issue: 7 Linguagem: Inglês

10.1083/jcb.200503023

ISSN

1540-8140

Autores

Kazuhisa Kinoshita, Tim L. Noetzel, Laurence Pelletier, Karl Mechtler, David Drechsel, Anne Schwager, Mike Lee, Jordan W. Raff, Anthony A. Hyman,

Tópico(s)

Epigenetics and DNA Methylation

Resumo

Centrosomes act as sites of microtubule growth, but little is known about how the number and stability of microtubules emanating from a centrosome are controlled during the cell cycle. We studied the role of the TACC3–XMAP215 complex in this process by using purified proteins and Xenopus laevis egg extracts. We show that TACC3 forms a one-to-one complex with and enhances the microtubule-stabilizing activity of XMAP215 in vitro. TACC3 enhances the number of microtubules emanating from mitotic centrosomes, and its targeting to centrosomes is regulated by Aurora A–dependent phosphorylation. We propose that Aurora A regulation of TACC3 activity defines a centrosome-specific mechanism for regulation of microtubule polymerization in mitosis.

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