TY - JOUR
T1 - Alp7/TACC is a crucial target in Ran-GTPase-dependent spindle formation in fission yeast
AU - Sato, Masamitsu
AU - Toda, Takashi
N1 - Funding Information:
Acknowledgements We thank E. Karsenti for comments and R. E. Carazo-Salas and M. Toya for critical reading of the manuscript, discussion and technical support for microscopy. We also thank M. Yoshida, H. Maekawa, E. Schiebel, I. Hagan, R. Y. Tsien, S. Yokobayashi and Y. Watanabe for plasmids and/or information. We are grateful to members of the Cell Regulation Laboratory and M. Yamamoto for support. This work is supported by Cancer Research UK. M.S. is a recipient of a Japan Society for the Promotion of Science (JSPS) Postdoctoral Fellowship for Research Abroad.
PY - 2007/5/17
Y1 - 2007/5/17
N2 - Microtubules are essential intracellular structures involved in several cellular phenomena, including polarity establishment and chromosome segregation. Because the nuclear envelope persists during mitosis (closed mitosis) in fission yeast (Schizosaccharomyces pombe), cytoplasmic microtubules must be reorganized into the spindle in the compartmentalized nucleus on mitotic entry. An ideal mechanism might be to take advantage of an evolutionarily conserved microtubule formation system that uses the Ran-GTPase nuclear transport machinery, but no targets of Ran for spindle formation have been identified in yeast. Here we show that a microtubule-associated protein, Alp7, which forms a complex with Alp14, is a target of Ran in yeast for spindle formation. The Ran-deficient pim1 mutant (pim1-F201S) failed to show mitosis-specific nuclear accumulation of Alp7. Moreover, this mutant exhibited compromised spindle formation and early mitotic delay. Importantly, these defects were suppressed by Alp7 that was artificially targeted to the nucleus by a Ran-independent and importin-α-mediated system. Thus, Ran targets Alp7-Alp14 to achieve nuclear spindle formation, and might differentiate its targets depending on whether the organism undergoes closed or open mitosis.
AB - Microtubules are essential intracellular structures involved in several cellular phenomena, including polarity establishment and chromosome segregation. Because the nuclear envelope persists during mitosis (closed mitosis) in fission yeast (Schizosaccharomyces pombe), cytoplasmic microtubules must be reorganized into the spindle in the compartmentalized nucleus on mitotic entry. An ideal mechanism might be to take advantage of an evolutionarily conserved microtubule formation system that uses the Ran-GTPase nuclear transport machinery, but no targets of Ran for spindle formation have been identified in yeast. Here we show that a microtubule-associated protein, Alp7, which forms a complex with Alp14, is a target of Ran in yeast for spindle formation. The Ran-deficient pim1 mutant (pim1-F201S) failed to show mitosis-specific nuclear accumulation of Alp7. Moreover, this mutant exhibited compromised spindle formation and early mitotic delay. Importantly, these defects were suppressed by Alp7 that was artificially targeted to the nucleus by a Ran-independent and importin-α-mediated system. Thus, Ran targets Alp7-Alp14 to achieve nuclear spindle formation, and might differentiate its targets depending on whether the organism undergoes closed or open mitosis.
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U2 - 10.1038/nature05773
DO - 10.1038/nature05773
M3 - Article
C2 - 17476213
AN - SCOPUS:34249103992
SN - 0028-0836
VL - 447
SP - 334
EP - 337
JO - Nature
JF - Nature
IS - 7142
ER -