4.4 Article

Measuring nanometer scale gradients in spindle microtubule dynamics using model convolution microscopy

Journal

MOLECULAR BIOLOGY OF THE CELL
Volume 17, Issue 9, Pages 4069-4079

Publisher

AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.E06-04-0312

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Funding

  1. NIGMS NIH HHS [R01 GM024364, R37 GM024364, GM32238, GM071522, K12 GM000678, R01 GM071522, GM24364, GM00678, R01 GM032238, R37 GM032238] Funding Source: Medline

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A computational model for the budding yeast mitotic spindle predicts a spatial gradient in tubulin turnover that is produced by kinetochore-attached microtubule (kMT) plus-end polymerization and depolymerization dynamics. However, kMTs in yeast are often much shorter than the resolution limit of the light microscope, making visualization of this gradient difficult. To overcome this limitation, we combined digital imaging of fluorescence redistribution after photo-bleaching (FRAP) with model convolution methods to compare computer simulations at nanometer scale resolution to microscopic data. We measured a gradient in microtubule dynamics in yeast spindles at similar to 65-nm spatial intervals. Tubulin turnover is greatest near kinetochores and lowest near the spindle poles. A beta-tubulin mutant with decreased plus-end dynamics preserves the spatial gradient in tubulin turnover at a slower time scale, increases average kinetochore microtubule length similar to 14%, and decreases tension at kinetochores. The beta-tubulin mutant cells have an increased frequency of chromosome loss, suggesting that the accuracy of chromosome segregation is linked to robust kMT plus-end dynamics.

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