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Updated: Jul 7, 2026

Spatio-Temporal Manipulation of Small GTPase Activity at Subcellular Level and on Timescale of Seconds in Living Cells
Published on: March 9, 2012
Importin beta is a mitotic target of the small GTPase Ran in spindle assembly
M V Nachury1, T J Maresca, W C Salmon
1Department of Molecular and Cell Biology, Division of Cell and Developmental Biology, University of California-Berkeley, Berkeley, CA 94720, USA.
The GTPase Ran, through importin beta, promotes spindle formation by releasing microtubule-organizing factors. This mechanism is crucial for organizing microtubules during cell division.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- The GTPase Ran's role in stimulating microtubule polymerization during mitosis is known, but its mechanism remains unclear.
- Nuclear transport factors like importin beta are implicated in various cellular processes.
Purpose of the Study:
- To elucidate the mechanism by which the GTPase Ran influences microtubule polymerization and spindle formation during mitosis.
- To investigate the role of importin beta in Ran-mediated mitotic events.
Main Methods:
- In vitro and in vivo experiments were conducted using mitotic extracts.
- Aster promoting activity (APA) was isolated and analyzed.
- The interaction between RanGTP, importin beta, and APA components like NuMA was studied.
Main Results:
- Importin beta was found to inhibit spindle formation and sequester aster promoting activity (APA).
- RanGTP releases APA components, including NuMA, from importin beta.
- Released APA components induce spindle-like structures independently of centrosomes, chromatin, or Ran.
Conclusions:
- RanGTP's mitotic function involves releasing cargoes from transport factors, similar to its interphase role.
- This mechanism promotes spindle assembly by organizing microtubules near chromosomes.
- Importin beta acts as a key mediator in Ran's regulation of mitotic spindle formation.
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