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.

PubMed

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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