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Forces acting on the fission yeast anaphase spindle
Cell Motility and the Cytoskeleton
|January 1, 1996
Summary
Fission yeast astral microtubules in a convergent orientation correlate with bowed mitotic spindles during anaphase B. This suggests astral microtubules may influence spindle forces and cell length regulation.
Area of Science:
- Cell Biology
- Microscopy
- Genetics
Background:
- The fission yeast mitotic spindle comprises three microtubule sets, including astral microtubules associated with spindle pole bodies.
- During anaphase B, astral microtubules can adopt parallel or convergent configurations.
- Fission yeast mitosis features an extended anaphase B, with spindle elongation crucial for cell division.
Purpose of the Study:
- To investigate the functional significance of astral microtubule configurations during anaphase B.
- To examine bowed spindle morphology in relation to astral microtubule orientation.
- To understand the role of astral microtubules in regulating mitotic spindle dynamics and cell length.
Main Methods:
- Indirect immunofluorescence microscopy was used to visualize mitotic spindles.
- Analysis of spindle morphology in wild-type and genetically modified fission yeast strains (overexpressing weel+ or inactivating cdc25+).
- Comparison of spindle length and astral microtubule configurations under different cellular conditions.
Main Results:
- Anaphase B spindles frequently appeared bowed specifically when astral microtubules were in a convergent orientation.
- Abnormally long spindles (up to 30 µm) in weel+ overexpressing or cdc25+ inactivated cells also exhibited bowing only with convergent astral microtubules.
- Bowed spindles were not observed when astral microtubules were in a parallel configuration.
Conclusions:
- Convergent astral microtubules are associated with bowed mitotic spindles in fission yeast.
- Astral microtubules may exert pulling forces on spindle poles or counteract forces from pole-to-pole microtubules.
- These findings offer insights into the mechanics of spindle elongation and cell length control during mitosis.