A Force-Induced Directional Switch of a Molecular Motor Enables Parallel Microtubule Bundle Formation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 27716509.
- Also identified by DOI 10.1016/j.cell.2016.09.029.
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Abstract
Microtubule-organizing centers (MTOCs) nucleate microtubules that can grow autonomously in any direction. To generate bundles of parallel microtubules originating from a single MTOC, the growth of multiple microtubules needs to coordinated, but the underlying mechanism is unknown. Here, we show that a conserved two-component system consisting of the plus-end tracker EB1 and the minus-end-directed molecular motor Kinesin-14 is sufficient to promote parallel microtubule growth. The underlying mechanism relies on the ability of Kinesin-14 to guide growing plus ends along existing microtubules. The generality of this finding is supported by yeast, Drosophila, and human EB1/Kinesin-14 pairs. We demonstrate that plus-end guiding involves a directional switch of the motor due to a force applied via a growing microtubule end. The described mechanism can account for the generation of parallel microtubule networks required for a broad range of cellular functions such as spindle assembly or cell polarization.
Medical subject headings
- Cell Cycle Proteins
- DNA Helicases
- Kinesins
- Microtubule Proteins
- Microtubule-Associated Proteins
- Microtubules
- Molecular Motor Proteins
- Oncogene Proteins
- RNA Helicases
- Saccharomyces cerevisiae Proteins