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Yeast 2-Cys peroxiredoxin Tsa1 protects cells from DNA damage-induced reactive oxygen species through peroxidase activity

Authors
Cui, JunLee, Sang YeolJang, Ho Hee
Issue Date
Dec-2015
Publisher
KOREAN SOC APPLIED BIOLOGICAL CHEMISTRY
Keywords
DNA damage; Hypersensitivity; Peroxidase activity; Peroxiredoxin; Reactive oxygen species; Saccharomyces cerevisiae
Citation
JOURNAL OF THE KOREAN SOCIETY FOR APPLIED BIOLOGICAL CHEMISTRY, v.58, no.6, pp.779 - 785
Journal Title
JOURNAL OF THE KOREAN SOCIETY FOR APPLIED BIOLOGICAL CHEMISTRY
Volume
58
Number
6
Start Page
779
End Page
785
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/9870
DOI
10.1007/s13765-015-0107-x
ISSN
1738-2203
Abstract
Peroxiredoxins (Prxs) belong to a family of thiol-specific peroxidases that scavenge reactive oxygen species (ROS). Yeast Prx thiol-specific antioxidant (Tsa1) protects cells from oxidative stress and maintains genome stability. In this study, we investigated the role of Tsa1 in the response to DNA damage. We observed that Tsa1 among all five Prxs of yeast is the most responsive in cell viability and mutation rate assays. The Delta tsa1 mutant is hypersensitive to DNA-damaging agents such as hydroxyurea, methyl methane sulfonate, and camptothecin. The Delta tsa1 cells lead to reduced cell viability and cell growth after DNA damage. The Delta tsa1-expressing wild-type Tsa1 rescues the sensitivity of Delta tsa1 cells to DNA damage, but not in Delta tsa1 cells carrying the active-site mutant Tsa1-C47S. We found that the level of ROS in Delta tsa1 cells was increased more than in wild-type cells by DNA damage. Tsa1 completely restored the production of DNA damage-induced ROS in Delta tsa1 cells, but not Tsa1-C47S. Finally, DNA damage-induced ROS resulted in a switch of Tsa1 from a low-molecular-weight to a high-molecular-weight complex. Taken together, these findings suggest that Tsa1 protects yeast cells from DNA damage by regulating the homeostasis of ROS through peroxidase activity.
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