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Updated: Jul 17, 2026

Microscopy of Fission Yeast Sexual Lifecycle
Published on: March 9, 2016
Myosin V-mediated vacuole distribution and fusion in fission yeast
D P Mulvihill1, P J Pollard, T Z Win
1Department of Biology, University College London, Gower Street, WC1E 6BT, London, United Kingdom.
Abstract:
The class V myosins are actin-based motors that move a variety of cellular cargoes [1]. In budding yeast, their activity includes the relocation of a portion of the vacuole from the mother cell to the bud [2, 3]. Fission yeast cells contain numerous (approximately 80) small vacuoles. When S. pombe cells are placed in water, vacuoles fuse in response to osmotic stress [4]. Fission yeast possess two type V myosin genes, myo51(+) and myo52(+) [5]. In a myo51Delta strain, vacuoles were distributed throughout the cell, and mean vacuole diameter was identical to that seen in wild-type cells. When myo51Delta and wild-type cells were placed in water, vacuoles enlarged by fusion. In myo52Delta cells, by contrast, vacuoles were smaller and mostly clustered around the nucleus, and fusion in water was largely inhibited. When cells containing GFP-Myo52 were placed in water, Myo52 was seen to redistribute from the cell poles to the surface of the fusing vacuoles. Vacuole fusion in fission yeast was inhibited by the microtubule drug thiabendazole (TBZ) but not by the actin inhibitor latrunculin B. This is the first demonstration of the involvement of a type V myosin, possibly via an interaction with microtubules, in homotypic membrane fusion.
Insights
Fission yeast type V myosins are crucial for vacuole fusion. Myo52 is essential for vacuole fusion, potentially interacting with microtubules during this process.
Area of Science:
- Cell Biology
- Molecular Motors
- Membrane Trafficking
Background:
- Class V myosins are motor proteins that transport cellular components.
- Fission yeast (S. pombe) utilize numerous small vacuoles for cellular functions.
- Vacuole fusion occurs in S. pombe under osmotic stress.
Purpose of the Study:
- To investigate the role of type V myosins in fission yeast vacuole fusion.
- To determine the specific functions of myo51(+) and myo52(+) in vacuole dynamics.
Main Methods:
- Gene deletion analysis of myo51(+) and myo52(+).
- Microscopy to observe vacuole distribution and fusion.
- Treatment with microtubule and actin inhibitors.
Main Results:
- Myo51 deletion did not affect vacuole distribution or size but allowed fusion.
- Myo52 deletion resulted in smaller, clustered vacuoles and inhibited fusion.
- Myo52 localized to fusing vacuoles, and fusion was sensitive to microtubule but not actin inhibitors.
Conclusions:
- Myo52 is essential for fission yeast vacuole fusion.
- Type V myosins, particularly Myo52, play a critical role in homotypic membrane fusion.
- Myo52 may interact with microtubules to facilitate vacuole fusion.
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