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MTOC formation during mitotic exit in fission yeast
M J Heitz1, J Petersen, S Valovin
1School of Biological Sciences, 2.205 Stopford Building, University of Manchester, Stopford Building, Oxford Road, Manchester M13 9PT, UK.
Journal of Cell Science
|January 17, 2002
Summary
The equatorial microtubule organizing center (MTOC) in fission yeast forms from gamma tubulin recruited to the F-actin ring during cell division. Its assembly requires the septation-inducing network and polo-like kinase, Plo1.
Area of Science:
- Cell Biology
- Cytoskeleton Dynamics
- Molecular Cell Biology
Background:
- Microtubules polymerize from nucleation templates containing gamma tubulin.
- Microtubule organizing centers (MTOCs) concentrate these templates.
- In Schizosaccharomyces pombe, an equatorial MTOC (EMTOC) forms during anaphase B and disassembles during cell separation.
Purpose of the Study:
- To investigate the formation and regulation of the equatorial MTOC during cytokinesis in Schizosaccharomyces pombe.
- To elucidate the relationship between the F-actin ring, the septation-inducing network (SIN), and MTOC assembly.
Main Methods:
- Recruitment of gamma tubulin to the equatorial F-actin ring.
- Analysis of EMTOC structure and integrity.
- Investigating the roles of the SIN and anaphase-promoting complex in EMTOC assembly.
- Examining the effect of Plo1 overproduction on EMTOC formation.
Main Results:
- The EMTOC is generated by recruiting gamma tubulin to the equatorial F-actin ring prior to cytokinesis.
- EMTOC structure is variable (horseshoe to bars) and depends on F-actin integrity, not microtubules.
- EMTOC assembly requires the SIN and anaphase-promoting complex.
- Plo1 overproduction induces EMTOC formation, suggesting a role in mitotic exit.
Conclusions:
- The equatorial MTOC formation is linked to F-actin ring constriction during cytokinesis.
- EMTOC assembly involves regulatory elements of cytokinesis but is more complex.
- Plo1 has an additional function in mitotic exit related to EMTOC formation.