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A more recent version of this article appeared on June 1, 2005
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Submitted on November 16, 2004
Revised on January 3, 2005
Accepted on January 5, 2005
Wellcome Trust Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3JR, United Kingdom
Monitoring Editor: Trisha Davis
From an insertional mutagenesis screen we isolated a novel gene, mto2+, involved in microtubule organization in fission yeast. mto2
strains are viable but exhibit defects in interphase microtubule nucleation and in formation of the postanaphase microtubule array at the end of mitosis. The mto2
defects represent a subset of the defects displayed by cells deleted for mto1+ (also known as mod20+ and mbo1+), a centrosomin-related protein required to recruit the gamma-tubulin complex to cytoplasmic microtubule-organizing centers (MTOCs). We show that mto2p colocalizes with mto1p at MTOCs throughout the cell cycle and that mto1p and mto2p coimmunoprecipitate from cytoplasmic extracts. In vitro studies suggest that mto2p binds directly to mto1p. In mto2
mutants, although some aspects of mto1p localization are perturbed, mto1p can still localize to spindle pole bodies and the cell division site, and to "satellite" particles on interphase microtubules. In mto1
mutants, localization of mto2p to all of these MTOCs is strongly reduced or absent altogether. We also find that in mto2
mutants, cytoplasmic forms of the gamma-tubulin complex are mislocalized, and the gamma-tubulin complex no longer coimmunoprecipitates with mto1p from cell extracts. These experiments establish mto2p as a major regulator of mto1p-mediated microtubule nucleation by the gamma-tubulin complex.
Corresponding author.
E-mail: ken.sawin{at}ed.ac.uk
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