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An essential function of the C. elegans ortholog of TPX2 is to localize activated aurora A kinase to mitotic spindles.

Dev. Cell. 2005 Aug;9(2):237-48
Nurhan Ozlü 1 , Martin Srayko , Kazuhisa Kinoshita , Bianca Habermann , Eileen T O'toole , Thomas Müller-Reichert , Natalie Schmalz , Arshad Desai , Anthony A Hyman
Nurhan Ozlü 1 , Martin Srayko , Kazuhisa Kinoshita , Bianca Habermann , Eileen T O'toole , Thomas Müller-Reichert , Natalie Schmalz , Arshad Desai , Anthony A Hyman
+ et al

[No authors listed]

Author information
  • 1 Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, Dresden 01307, Germany. ozlu@mpi-cbg.de

摘要


In vertebrates, the microtubule binding protein TPX2 is required for meiotic and mitotic spindle assembly. TPX2 is also known to bind to and activate Aurora A kinase and target it to the spindle. However, the relationship between the TPX2-Aurora A interaction and the role of TPX2 in spindle assembly is unclear. Here, we identify TPXL-1, a C. elegans protein that is the first characterized invertebrate ortholog of TPX2. We demonstrate that an essential role of TPXL-1 during mitosis is to activate and target Aurora A to microtubules. Our data suggest that this targeting stabilizes microtubules connecting kinetochores to the spindle poles. Thus, activation and targeting of Aurora A appears to be an ancient and conserved function of TPX2 that plays a central role in mitotic spindle assembly.