Spindle pole body duplication defective yeast cells are more prone to membrane damage

Hatice Büşra Konuk1, Bengü Ergüden1

  • 1Department of Bioengineering, Gebze Technical University, Gebze 41400, Kocaeli, Turkey.

Mycologia
|October 10, 2019
PubMed

Insights

Yeast cells with defective spindle pole body (SPB) duplication and active SESA complex show increased membrane susceptibility to essential oils, impacting cell integrity.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Mycology

Background:

  • Chromosome segregation during mitosis is crucial for preventing genetic instability.
  • Spindle pole body (SPB) duplication is essential for accurate chromosome separation.
  • The MonoPolar Spindle 2 (MPS2) protein is vital for SPB insertion into the nuclear envelope.

Purpose of the Study:

  • To investigate the impact of essential oils on yeast cell membranes.
  • To explore the relationship between the SESA complex, SPB duplication, and membrane integrity.
  • To understand how genetic defects in SPB duplication affect susceptibility to essential oils.

Main Methods:

  • Utilizing yeast strains with defective SPB duplication (mps2∆ 2µm-SMY2 and mps2∆ pom34∆).
  • Activating the SESA complex in these yeast strains.
  • Treating yeast cells with various essential oils.
  • Assessing yeast cell membrane damage post-treatment.

Main Results:

  • Yeast cells with active SESA complex and defective SPB duplication exhibit heightened sensitivity to essential oil-induced membrane damage.
  • The SESA complex, known to influence membrane lipid composition, plays a role in this increased susceptibility.
  • Essential oils compromise the membrane integrity of these genetically modified yeast cells.

Conclusions:

  • The SESA complex and SPB duplication status significantly influence yeast cell membrane's response to essential oils.
  • Essential oils pose a greater risk to yeast cells with compromised SPB duplication mechanisms.
  • This study links genetic factors affecting cell division to susceptibility to external membrane-disrupting agents.

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