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Observing Mitotic Division and Dynamics in a Live Zebrafish Embryo
Published on: July 15, 2016
Altered cohesin dynamics and H3K9 modifications contribute to mitotic defects in the cbf11Δ lipid metabolism mutant
Akshay Vishwanatha1, Jarmila Princová1, Patrik Hohoš1
1Laboratory of Microbial Genomics, Department of Cell Biology, Faculty of Science, Charles University, Viničná 7, Prague 2, Prague 128 00, Czech Republic.
Abstract:
Mitotic fidelity is crucial for the faithful distribution of genetic information into the daughter cells. Many fungal species, including the fission yeast Schizosaccharomyces pombe, undergo a closed form of mitosis, during which the nuclear envelope does not break down. In S. pombe, numerous processes have been identified that contribute to successful completion of mitosis. Notably, perturbations of lipid metabolism can lead to catastrophic mitosis and the 'cut' phenotype. It has been suggested that these mitotic defects are caused by insufficient membrane phospholipid supply during the anaphase nuclear expansion. However, it is not clear whether additional factors are involved. In this study, we characterized in detail mitosis in an S. pombe mutant lacking the Cbf11 transcription factor, which regulates lipid metabolism genes. We show that in cbf11Δ cells mitotic defects have already appeared prior to anaphase, before the nuclear expansion begins. Moreover, we identify altered cohesin dynamics and centromeric chromatin structure as additional factors affecting mitotic fidelity in cells with disrupted lipid homeostasis, providing new insights into this fundamental biological process.
Insights
Mitotic fidelity is essential for cell division. Disrupting lipid metabolism in fission yeast (Schizosaccharomyces pombe) causes early mitotic defects, involving cohesin and centromeric chromatin, not just membrane supply.
Area of Science:
- Cell Biology
- Genetics
- Molecular Biology
Background:
- Mitotic fidelity ensures accurate genetic distribution.
- Fission yeast (Schizosaccharomyces pombe) exhibits closed mitosis.
- Lipid metabolism disruptions can cause mitotic defects like the 'cut' phenotype.
Purpose of the Study:
- To investigate the role of the Cbf11 transcription factor in mitosis.
- To elucidate the mechanisms underlying mitotic defects in lipid metabolism mutants.
- To identify factors beyond membrane supply contributing to mitotic fidelity loss.
Main Methods:
- Characterization of mitosis in cbf11Δ S. pombe mutants.
- Analysis of mitotic progression before anaphase.
- Assessment of cohesin dynamics and centromeric chromatin structure.
Main Results:
- Mitotic defects in cbf11Δ cells precede nuclear expansion.
- Altered cohesin dynamics were observed.
- Changes in centromeric chromatin structure were identified.
Conclusions:
- Mitotic fidelity is compromised early in cbf11Δ cells, prior to anaphase.
- Cohesin dynamics and centromeric chromatin are critical factors in lipid homeostasis-related mitotic defects.
- These findings offer new insights into the regulation of mitosis and lipid metabolism.
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