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pubmed-article:12577065pubmed:abstractTextThe activated form of Ran (Ran-GTP) stimulates spindle assembly in Xenopus laevis egg extracts, presumably by releasing spindle assembly factors, such as TPX2 (target protein for Xenopus kinesin-like protein 2) and NuMA (nuclear-mitotic apparatus protein) from the inhibitory binding of importin-alpha and -beta. We report here that Ran-GTP stimulates the interaction between TPX2 and the Xenopus Aurora A kinase, Eg2. This interaction causes TPX2 to stimulate both the phosphorylation and the kinase activity of Eg2 in a microtubule-dependent manner. We show that TPX2 and microtubules promote phosphorylation of Eg2 by preventing phosphatase I (PPI)-induced dephosphorylation. Activation of Eg2 by TPX2 and microtubules is inhibited by importin-alpha and -beta, although this inhibition is overcome by Ran-GTP both in the egg extracts and in vitro with purified proteins. As the phosphorylation of Eg2 stimulated by the Ran-GTP-TPX2 pathway is essential for spindle assembly, we hypothesize that the Ran-GTP gradient established by the condensed chromosomes is translated into the Aurora A kinase gradient on the microtubules to regulate spindle assembly and dynamics.lld:pubmed
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pubmed-article:12577065pubmed:articleTitleA Ran signalling pathway mediated by the mitotic kinase Aurora A in spindle assembly.lld:pubmed
pubmed-article:12577065pubmed:affiliationDepartment of Embryology, Carnegie Institution of Washington/Howard Hughes Medical Institute, Baltimore, MD 21210, USA.lld:pubmed
pubmed-article:12577065pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12577065pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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