Killer double-stranded ribonucleic acid synthesis in cell division cycle mutants of Saccharomyces cerevisiae

Journal of Bacteriology
|September 1, 1977
PubMed

Insights

Killer yeast strains with defects in initiating DNA replication or nuclear division overproduce double-stranded RNA (dsRNA) at restrictive temperatures. This overproduction requires the complete dsRNA genome, highlighting its role in DNA replication control.

Area of Science:

  • Molecular Biology
  • Yeast Genetics
  • RNA Synthesis

Background:

  • Killer Saccharomyces cerevisiae possess double-stranded RNA (dsRNA) viruses.
  • Cell division cycle (cdc) mutants affect DNA replication and nuclear division.
  • Understanding dsRNA synthesis regulation is crucial for yeast genetics.

Purpose of the Study:

  • Investigate the relationship between cell division cycle mutations and killer dsRNA synthesis.
  • Determine which stages of DNA replication and nuclear division impact dsRNA overproduction.
  • Identify the role of the complete dsRNA genome in this phenomenon.

Main Methods:

  • Utilized seven distinct Saccharomyces cerevisiae cell division cycle mutants.
  • Assessed dsRNA synthesis levels at restrictive temperatures.
  • Examined killer sensitive strains to confirm genome requirements.

Main Results:

  • Overproduction of killer dsRNA observed in mutants defective in DNA replication initiation (cdc28, cdc4, cdc7) and nuclear division (cdc23, cdc14).
  • No dsRNA overproduction occurred in mutants defective in DNA chain elongation (cdc8, cdc21).
  • Complete killer dsRNA genome essential for temperature-induced overproduction.

Conclusions:

  • Specific defects in DNA replication initiation and nuclear division trigger killer dsRNA overproduction.
  • DNA replication elongation stages are not linked to this dsRNA overproduction.
  • The killer dsRNA genome plays a critical role in regulating its own synthesis in response to cell cycle perturbations.

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