Molecular & Cellular Toxicology

, Volume 15, Issue 1, pp 65–73 | Cite as

Chronological lifespan regulation of Saccharomyces cerevisiae by leucine biosynthesis pathway genes via TOR1 and COX2 expression regulation

  • Choco Michael Gorospe
  • Sung-Lim Yu
  • Mi-Sun Kang
  • Sung-Keun LeeEmail author
Original Paper



Leucine is involved in various cellular mechanisms, including protein metabolism, insulin signaling, and longevity control. Nevertheless, the contribution of leucine metabolism genes to longevity have not been thoroughly studied.


Several mutants of leucine biosynthesis genes were constructed, and their effect on yeast lifespan and various phenotypes were examined.


Several deletion mutants increase yeast lifespan. Among those, LEU2 and leu4Δ cells exhibit significantly increased lifespan, moderately increased reactive oxygen species (ROS) generation, decreased Tor1p expression, significantly increased expression of a cytochrome c oxidase subunit, and decreased cell death. In these cells, reduced Tor1p seemed to stimulate a slight increase in ROS generation which stimulates Cox2p expression that can prevent cellular damage. Indeed, the rate of cell death of LEU2 and leu4Δ cells was drastically decreased.


LEU2 and LEU4 seem critical in determining yeast lifespan by providing a hormetic effect that promotes yeast longevity.


Yeast Leucine LEU2 LEU4 Chronological lifespan 


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Copyright information

© The Korean Society of Toxicogenomics and Toxicoproteomics and Springer Nature B.V. 2019

Authors and Affiliations

  • Choco Michael Gorospe
    • 1
  • Sung-Lim Yu
    • 2
  • Mi-Sun Kang
    • 3
  • Sung-Keun Lee
    • 1
    • 3
    Email author
  1. 1.Department of Molecular BiomedicineInha UniversityIncheonRepublic of Korea
  2. 2.Inha Research Institute for Medical SciencesInha UniversityIncheonRepublic of Korea
  3. 3.Department of Pharmacology, College of MedicineInha UniversityIncheonRepublic of Korea

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