Directly probing the mechanical properties of the spindle and its matrix

dc.contributor.author Gatlin, Jesse C.
dc.contributor.author Matov, Alexandre
dc.contributor.author Danuser, Gaudenz
dc.contributor.author Mitchison, Timothy J.
dc.contributor.author Salmon, Edward D.
dc.date.accessioned 2010-10-29T16:38:25Z
dc.date.available 2010-10-29T16:38:25Z
dc.date.issued 2010-02-22
dc.description © The Authors, 2010. This article is distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. The definitive version was published in Journal of Cell Biology 188 (2010): 481-489, doi:10.1083/jcb.200907110. en_US
dc.description.abstract Several recent models for spindle length regulation propose an elastic pole to pole spindle matrix that is sufficiently strong to bear or antagonize forces generated by microtubules and microtubule motors. We tested this hypothesis using microneedles to skewer metaphase spindles in Xenopus laevis egg extracts. Microneedle tips inserted into a spindle just outside the metaphase plate resulted in spindle movement along the interpolar axis at a velocity slightly slower than microtubule poleward flux, bringing the nearest pole toward the needle. Spindle velocity decreased near the pole, which often split apart slowly, eventually letting the spindle move completely off the needle. When two needles were inserted on either side of the metaphase plate and rapidly moved apart, there was minimal spindle deformation until they reached the poles. In contrast, needle separation in the equatorial direction rapidly increased spindle width as constant length spindle fibers pulled the poles together. These observations indicate that an isotropic spindle matrix does not make a significant mechanical contribution to metaphase spindle length determination. en_US
dc.description.sponsorship This work was supported by National Institute of General Medicine grants to J.C. Gatlin (F32GM080049) and E.D. Salmon (GM24364). T.J. Mitchison was funded by a grant from the National Cancer Institute (CA078048-09). en_US
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dc.identifier.citation Journal of Cell Biology 188 (2010): 481-489 en_US
dc.identifier.doi 10.1083/jcb.200907110
dc.identifier.uri https://hdl.handle.net/1912/4028
dc.language.iso en_US en_US
dc.publisher Rockefeller University Press en_US
dc.relation.uri https://doi.org/10.1083/jcb.200907110
dc.rights Attribution-NonCommercial-ShareAlike 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/3.0/us/ *
dc.title Directly probing the mechanical properties of the spindle and its matrix en_US
dc.type Article en_US
dspace.entity.type Publication
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relation.isAuthorOfPublication.latestForDiscovery 8c53525b-6f41-469f-b920-bdcfd75fb018
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Video 1: Time-lapse fluorescence imaging of spindle escape off a single skewering needle.
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Video 2: Time-lapse fluorescence imaging of two spindles in the same frame escaping their needles in different directions.
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Video 3: Time-lapse fluorescence imaging of a skewering needle moving through a spindle pole.
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