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Published on: November 20, 2021
FSH1 overexpression triggers apoptosis in Saccharomyces cerevisiae
Ramachandran Gowsalya1, Chidambaram Ravi1, Mathivanan Arul1
1Department of Biochemistry, School of Life Sciences, Bharathidasan University, Tiruchirappalli, Tamil Nadu, 620024, India.
Abstract:
FSH1 belongs to the family of serine hydrolases in yeast and is homologous to the human ovarian tumor suppressor gene (OVAC2). Our preliminary results showed that cells lacking Fsh1p exhibit an increase in cell growth, and a decrease in the expression of AIF1 and NUC1 (apoptosis responsive genes) when compared to the wild type cells. Growth inhibition of cells overexpressing FSH1 is due to induction of cell death associated with cell death markers typical of mammalian apoptosis namely DNA fragmentation, phosphatidylserine externalization, ROS accumulation, Cytochrome c release, and altered mitochondrial membrane potential. When wild type cells were overexpressed with FSH1 there was up regulation of AIF1 level when compared to control cells suggesting that overexpression of FSH1 regulated cell death in yeast.
Insights
FSH1 gene overexpression in yeast induces cell death, mimicking mammalian apoptosis. Deleting FSH1 increases cell growth and reduces apoptosis markers, suggesting FSH1 regulates cell death pathways.
Area of Science:
- Molecular Biology
- Yeast Genetics
- Cell Death Research
Background:
- FSH1 is a serine hydrolase in yeast, homologous to human OVAC2.
- Preliminary data suggests Fsh1p influences cell growth and apoptosis gene expression.
Purpose of the Study:
- To investigate the role of FSH1 in yeast cell death.
- To determine if FSH1 overexpression induces apoptosis-like phenotypes in yeast.
Main Methods:
- Gene knockout and overexpression in yeast (Saccharomyces cerevisiae).
- Analysis of cell growth rates.
- Assessment of apoptosis markers: DNA fragmentation, phosphatidylserine externalization, ROS accumulation, Cytochrome c release, mitochondrial membrane potential.
Main Results:
- FSH1 deletion increased cell growth and decreased apoptosis-responsive genes (AIF1, NUC1).
- FSH1 overexpression inhibited growth and induced mammalian-like apoptosis markers.
- Overexpression of FSH1 upregulated AIF1 levels in wild-type cells.
Conclusions:
- FSH1 plays a critical role in regulating cell death in yeast.
- FSH1 overexpression can induce apoptosis through conserved molecular pathways.
- FSH1 is a potential target for modulating cell death in yeast models.
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