Cdk11 is a RanGTP-dependent microtubule stabilization factor that regulates spindle assembly rate

Author:

Yokoyama Hideki1,Gruss Oliver J.2,Rybina Sofia1,Caudron Maïwen1,Schelder Malgorzata1,Wilm Matthias1,Mattaj Iain W.1,Karsenti Eric1

Affiliation:

1. European Molecular Biology Laboratory, Heidelberg 69117, Germany

2. Zentrum für Molekulare Biologie der Universität Heidelberg, 69120 Heidelberg, Germany

Abstract

Production of Ran–guanosine triphosphate (GTP) around chromosomes induces local nucleation and plus end stabilization of microtubules (MTs). The nuclear protein TPX2 is required for RanGTP-dependent MT nucleation. To find the MT stabilizer, we affinity purify nuclear localization signal (NLS)–containing proteins from Xenopus laevis egg extracts. This NLS protein fraction contains the MT stabilization activity. After further purification, we used mass spectrometry to identify proteins in active fractions, including cyclin-dependent kinase 11 (Cdk11). Cdk11 localizes on spindle poles and MTs in Xenopus culture cells and egg extracts. Recombinant Cdk11 demonstrates RanGTP-dependent MT stabilization activity, whereas a kinase-dead mutant does not. Inactivation of Cdk11 in egg extracts blocks RanGTP-dependent MT stabilization and dramatically decreases the spindle assembly rate. Simultaneous depletion of TPX2 completely inhibits centrosome-dependent spindle assembly. Our results indicate that Cdk11 is responsible for RanGTP-dependent MT stabilization around chromosomes and that this local stabilization is essential for normal rates of spindle assembly and spindle function.

Publisher

Rockefeller University Press

Subject

Cell Biology

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