Importin α/β and Ran-GTP Regulate XCTK2 Microtubule Binding Through a Bipartite Nuclear Localization Signal

Stephanie C. Ems-McClung, Yixian Zheng, Claire Walczak

Research output: Contribution to journalArticle

103 Citations (Scopus)

Abstract

The small GTPase Ran is essential for spindle assembly. Ran is proposed to act through its nuclear import receptors importin α and/or importin β to control the sequestration of proteins necessary for spindle assembly. To date, the molecular mechanisms by which the Ran pathway functions remain unclear. Using purified proteins, we have reconstituted Ran-regulated microtubule binding of the C-terminal kinesin XCTK2, a kinesin important for spindle assembly. We show that the tail of XCTK2 binds to microtubules and that this binding is inhibited in the presence of importin α and β and (α/β) and restored by addition of Ran-GTP. The bipartite nuclear localization signal (NLS) in the tail of XCTK2 is essential to this process, because mutation of the NLS abolishes importin α/β-mediated regulation of XCTK2 microtubule binding. Our data show that importin α/β directly regulates the activity of XCTK2 and that one of the molecular mechanisms of Ran-regulated spindle assembly is identical to that used in classical NLS-driven nuclear transport.

Original languageEnglish
Pages (from-to)46-57
Number of pages12
JournalMolecular Biology of the Cell
Volume15
Issue number1
DOIs
StatePublished - Jan 2004

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Karyopherins
Nuclear Localization Signals
Guanosine Triphosphate
Microtubules
Kinesin
Cell Nucleus Active Transport
Monomeric GTP-Binding Proteins
Cytoplasmic and Nuclear Receptors
Proteins
Mutation

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cell Biology

Cite this

Importin α/β and Ran-GTP Regulate XCTK2 Microtubule Binding Through a Bipartite Nuclear Localization Signal. / Ems-McClung, Stephanie C.; Zheng, Yixian; Walczak, Claire.

In: Molecular Biology of the Cell, Vol. 15, No. 1, 01.2004, p. 46-57.

Research output: Contribution to journalArticle

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