Organization of the Smallest Eukaryotic Spindle
- Creators
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Gan, Lu
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Ladinsky, Mark S.
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Jensen, Grant J.
Abstract
In metazoans, plants, and fungi, the spindle checkpoint delays mitosis until each chromosome is attached to one or more of its own kinetochore microtubules (kMTs). Some unicellular eukaryotes, however, have been reported to have fewer kMTs than chromosomes. If this is the case, it is unclear how the spindle checkpoint could be satisfied. In the vast majority of the previous studies, mitotic cells were chemically fixed at room temperature, but this does not always preserve dynamic and/or small structures like spindle MTs and kinetochores. Indeed, later higher-resolution studies have reversed some earlier claims. Here we show that in Ostreococcus tauri (the smallest eukaryote known), mitosis does involve fewer spindle microtubules than chromosomes. O. tauri cultures were enriched for mitotic cells, high-pressure frozen, and then imaged in 3D both in plastic and in a near-native ("frozen-hydrated") state through electron tomography. Mitotic cells have a distinctive intranuclear heterochromatin-free "spindle tunnel" with approximately four short and occasionally one long, incomplete (unclosed) microtubule at each end of the spindle tunnel. Because other aspects of O. tauri's spindle checkpoint seem typical, these data suggest that O. tauri's 20 chromosomes are physically linked and segregated as just one or a small number of groups.
Additional Information
© 2011 Elsevier Ltd. Received 4 November 2010; revised 17 June 2011; Accepted 9 August 2011. Published online: September 8, 2011. Available online 8 September 2011. We thank G. Henderson, P. Dias, A. McDowall, F.-Y. Bouget, H. Moreau, W. Marshall, J. Azimzadeh, and G. Ou for discussions and the anonymous reviewers for helpful comments. This work was supported in part by National Institutes of Health (NIH) grant P50 GM082545 to G.J.J. and a gift to the California Institute of Technology from the Gordon and Betty Moore Foundation. L.G. is a Damon Runyon Fellow supported by a fellowship from the Damon Runyon Cancer Research Foundation (DRG-1940-07). M.S.L. was supported by NIH grant 2 R37 AI041239-06A1 to P. Björkman.Attached Files
Accepted Version - nihms328861.pdf
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Additional details
- PMCID
- PMC3234289
- Eprint ID
- 27345
- Resolver ID
- CaltechAUTHORS:20111021-085847452
- NIH
- P50 GM082545
- Gordon and Betty Moore Foundation
- Damon Runyon Cancer Research Foundation
- DRG-1940-07
- NIH
- 2 R37 AI041239-06A1
- Created
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2011-10-21Created from EPrint's datestamp field
- Updated
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2021-11-09Created from EPrint's last_modified field