4.7 Article

Importin-β Directly Regulates the Motor Activity and Turnover of a Kinesin-4

Journal

DEVELOPMENTAL CELL
Volume 44, Issue 5, Pages 642-+

Publisher

CELL PRESS
DOI: 10.1016/j.devcel.2018.01.027

Keywords

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Funding

  1. Monsanto/Norman Borlaug Corporate Fellowship
  2. Center for Lignocellulose Structure and Formation
  3. Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0001090]
  4. National Science Foundation [MCB-1121287]
  5. Center for Engineering Mechanobiology [CMMI-1548571]
  6. Directorate For Engineering
  7. Div Of Civil, Mechanical, & Manufact Inn [1548571] Funding Source: National Science Foundation

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Spatiotemporal regulation of kinesins is essential for microtubule-dependent intracellular transport. In plants, cell wall deposition depends on the FRA1 kinesin, whose abundance and motility are tightly controlled to match cellular growth rate. Here, we show that an importin-beta, IMB4, regulates FRA1 activity in a developmental manner. IMB4 physically interacts with a PY motif in the FRA1 motor domain and inhibits its motility by preventing microtubule binding, while also protecting FRA1 against proteasome-mediated degradation, thus providing a mechanism to couple the motility and stability of FRA1. This regulatory mechanism is likely to be broadly applicable, based on the conservation of the PY motif in the motor domains of plant and animal kinesins and the direct interaction of multiple plant kinesins with IMB4. Together, our data establish IMB4 as a multi-functional regulator of FRA1 and reveal a mechanism for how plants control the magnitude of cargo transport needed for cell wall assembly.

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