Publication

Human TPX2 is required for targeting Aurora-A kinase to the spindle

Kufer, T. A., Silljé, H. H. W., Körner, R., Gruss, O. J., Meraldi, P. & Nigg, E. A., 19-Aug-2002, In : Journal of Cell Biology. 158, 4, p. 617-23 7 p.

Research output: Contribution to journalArticleAcademicpeer-review

Aurora-A is a serine-threonine kinase implicated in the assembly and maintenance of the mitotic spindle. Here we show that human Aurora-A binds to TPX2, a prominent component of the spindle apparatus. TPX2 was identified by mass spectrometry as a major protein coimmunoprecipitating specifically with Aurora-A from mitotic HeLa cell extracts. Conversely, Aurora-A could be detected in TPX2 immunoprecipitates. This indicates that subpopulations of these two proteins undergo complex formation in vivo. Binding studies demonstrated that the NH2 terminus of TPX2 can directly interact with the COOH-terminal catalytic domain of Aurora-A. Although kinase activity was not required for this interaction, TPX2 was readily phosphorylated by Aurora-A. Upon siRNA-mediated elimination of TPX2 from cells, the association of Aurora-A with the spindle microtubules was abolished, although its association with spindle poles was unaffected. Conversely, depletion of Aurora-A by siRNA had no detectable influence on the localization of TPX2. We propose that human TPX2 is required for targeting Aurora-A kinase to the spindle apparatus. In turn, Aurora-A might regulate the function of TPX2 during spindle assembly.

Original languageEnglish
Pages (from-to)617-23
Number of pages7
JournalJournal of Cell Biology
Volume158
Issue number4
Publication statusPublished - 19-Aug-2002
Externally publishedYes

    Keywords

  • Aurora Kinases, Cell Cycle Proteins, Enzyme Activation, HeLa Cells, Humans, Macromolecular Substances, Microtubule-Associated Proteins, Microtubules, Mitosis, Neoplasm Proteins, Nuclear Proteins, Phosphoproteins, Precipitin Tests, Protein Binding, Protein Kinases, Protein-Serine-Threonine Kinases, RNA, Small Interfering, RNA, Untranslated, Spindle Apparatus, Substrate Specificity, Xenopus Proteins

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