| Literature DB >> 32531285 |
Zachary M Geisterfer1, Daniel Y Zhu2, Timothy J Mitchison3, John Oakey4, Jesse C Gatlin5.
Abstract
The microtubule cytoskeleton plays critically important roles in numerous cellular functions in eukaryotes, and it does so across a functionally diverse and morphologically disparate range of cell types [1]. In these roles, microtubule assemblies must adopt distinct morphologies and physical dimensions to perform specific functions [2-5]. As such, these macromolecular assemblies-as well as the dynamics of the individual microtubule polymers from which they are made-must scale and change in accordance with cell size, geometry, and function. Microtubules in cells typically assemble to a steady state in mass, leaving enough of their tubulin subunits soluble to allow rapid growth and turnover. This suggests some negative feedback that limits the extent of assembly, for example, decrease in growth rate, or increase in catastrophe rate, as the soluble subunit pool decreases. Although these ideas have informed the field for decades, they have not been observed experimentally. Here, we describe the application of an experimental approach that combines cell-free extracts with photo-patterned hydrogel micro-enclosures as a means to investigate microtubule dynamics in cytoplasmic volumes of defined size and shape. Our measurements reveal a negative correlation between microtubule plus-end density and microtubule growth rates and suggest that these rates are sensitive to the presence of nearby growing ends.Entities:
Keywords: Xenopus extracts; cytoskeleton; microfluidics; microtubule aster; microtubule dynamics; microtubules; tubulin
Year: 2020 PMID: 32531285 PMCID: PMC7416492 DOI: 10.1016/j.cub.2020.05.056
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834