Abstract

The ability to survive stressful conditions is important for every living cell. Certain stresses not only affect the current well-being of cells but may also have far-reaching consequences. Uncurbed oxidative stress can cause DNA damage and decrease cell survival and/or increase mutation rates, and certain substances that generate oxidative damage in the cell mainly act on DNA. Radiomimetic zeocin causes oxidative damage in DNA, predominantly by inducing single- or double-strand breaks. Such lesions can lead to chromosomal rearrangements, especially in diploid cells, in which the two sets of chromosomes facilitate excessive and deleterious recombination. In a global screen for zeocin-oversensitive mutants, we selected 133 genes whose deletion reduces the survival of zeocin-treated diploid Saccharomyces cerevisiae cells. The screen revealed numerous genes associated with stress responses, DNA repair genes, cell cycle progression genes, and chromatin remodeling genes. Notably, the screen also demonstrated the involvement of the vesicular trafficking system in cellular protection against DNA damage. The analyses indicated the importance of vesicular system integrity in various pathways of cellular protection from zeocin-dependent damage, including detoxification and a direct or transitional role in genome maintenance processes that remains unclear. The data showed that deleting genes involved in vesicular trafficking may lead to Rad52 focus accumulation and changes in total DNA content or even cell ploidy alterations, and such deletions may preclude proper DNA repair after zeocin treatment. We postulate that functional vesicular transport is crucial for sustaining an integral genome. We believe that the identification of numerous new genes implicated in genome restoration after genotoxic oxidative stress combined with the detected link between vesicular trafficking and genome integrity will reveal novel molecular processes involved in genome stability in diploid cells.

Highlights

  • Living cells have developed various mechanisms to detect and repair damage that occurs under stress conditions

  • To shed more light on these issues, we studied the cellular commitments of zeocin, which is one of the oxidative agents, and applied a genome-wide approach using a Saccharomyces cerevisiae diploid yeast knock-out collection (YKO) generated by the Saccharomyces Genome Deletion Project Consortium [34] together with the barcode microarray technique

  • Our clone set included more than 5,000 homodiploid strains carrying double deletions of non-essential genes (HD) and approximately 1,100 heterodiploid strains in which one copy of an essential gene was removed from the cell genome (ESS)

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Summary

Introduction

Living cells have developed various mechanisms to detect and repair damage that occurs under stress conditions. The results appeared to indicate that for survival under zeocin stress conditions, functional vesicular trafficking is as important as DNA damage recognition and repair pathways.

Results
Conclusion
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