Killer double-stranded ribonucleic acid synthesis in cell division cycle mutants of Saccharomyces cerevisiae
Abstract:
The synthesis of killer double-stranded ribonucleic acid (dsRNA) in Saccharomyces cerevisiae was examined in seven different cell division cycle mutants (cdc) that are defective in nuclear deoxyribonucleic acid replication and contain the "killer character." In cdc28, cdc4, and cdc7, which are defective in the initiation of nuclear deoxyribonucleic acid synthesis, and in cdc23 or in cdc14, defective in medial or late nuclear division, an overproduction of dsRNA at the restrictive temperature was observed. In contrast to the above mutants, the synthesis of killer dsRNA is not enhanced at the restrictive temperature in either cdc8 or cdc21, which are defective in deoxyribonucleic acid chain elongation. Examination of killer sensitive strains (cdc7 K- and cdc4 K-) has shown that the complete killer dsRNA genome is essential for the overproduction of dsRNA at the restrictive temperature.
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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