Discovery and identification of genes involved in DNA damage repair in yeast

Sasi Kumar Jagadeesan1, Taylor Potter1, Mustafa Al-Gafari1

  • 1Ottawa Institute of Systems Biology, University of Ottawa, Ottawa, Ontario, Canada; Department of Biology, Carleton University, Ottawa, Ontario, Canada.

Gene
|May 15, 2022
PubMed

Insights

Researchers identified three new genes, GAL7, YMR130W, and YHI9, involved in DNA double-strand break (DSB) repair pathways like Homologous Recombination (HR) and Non-Homologous End Joining (NHEJ) in yeast.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • DNA double-strand breaks (DSBs) are critical DNA lesions that threaten cellular integrity.
  • Defects in DSB repair are common in cancer cells, leading to genomic instability.
  • While DSB repair mechanisms are known, novel contributing genes are continuously being discovered.

Purpose of the Study:

  • To computationally identify novel genes involved in DNA damage repair pathways.
  • To investigate the roles of previously uncharacterized genes in DSB repair in Saccharomyces cerevisiae.

Main Methods:

  • Utilized a computational approach to predict novel DNA repair genes.
  • Selected candidate genes GAL7, YMR130W, and YHI9 for experimental validation.
  • Performed laboratory testing on deletion strains (gal7Δ, ymr130wΔ, yhi9Δ).
  • Conducted genetic interaction analysis, including with chromatin regulators SIR2, SIR3, and SIR4.

Main Results:

  • GAL7, YMR130W, and YHI9 were implicated in Homologous Recombination (HR) and/or Non-Homologous End Joining (NHEJ) pathways.
  • Deletion mutants exhibited increased sensitivity to DNA damage-inducing agents.
  • These genes interact with chromatin regulators (SIR2, SIR3, SIR4) within the DNA damage repair network.

Conclusions:

  • GAL7, YMR130W, and YHI9 are novel participants in yeast DNA double-strand break repair.
  • These findings expand our understanding of the complex DNA damage repair machinery.
  • The study highlights the interconnectedness of DNA repair and chromatin regulation.

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