YCR095C
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| Systematic name | YCR095C |
| Gene name | OCA4 |
| Aliases | |
| Feature type | ORF, Uncharacterized |
| Coordinates | Chr III:289258..288170 |
| Primary SGDID | S000000691 |
Description of YCR095C: Cytoplasmic protein required for replication of Brome mosaic virus in S. cerevisiae, which is a model system for studying replication of positive-strand RNA viruses in their natural hosts[1][2]
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Contents
Community Commentary
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Ethanol
YCR095C cell growth started off at a higher growth rate but decreased at an earlier rate. The doubling time is 60.40. Ethanol might have affected the growth of the cells during the end, but not early growth.
Caffeine
Interpretation
The average doubling time for the YCR095C (C6) gene in standard conditions was 99 minutes. Under caffeine stress, the average doubling time was 344 minutes. That is a 237% increase in doubling time which means that cell growth was negatively affected (slowed down) by this type of stress.
Hydrogen Peroxide
This is the link to the protocol page: UW-Stout/Hydrogen Peroxide FA22.
The doubling time for the YCR095C under stressed conditions is 432 minutes and with no stress it is 204 minutes. The BY4375 under stress had a 598 minute doubling time and with no stress there was a 229 minute doubling time. The YCR095 gene had a faster doubling time than the wild type yeast, therefore is more resistant to the hydrogen peroxide stress. There is a chance this was due to experimental error such as not vortexing the wild type yeast or having other microorganisms on your gloves.
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References
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- ↑ Huh WK, et al. (2003) Global analysis of protein localization in budding yeast. Nature 425(6959):686-91 SGD PMID 14562095
- ↑ Kushner DB, et al. (2003) Systematic, genome-wide identification of host genes affecting replication of a positive-strand RNA virus. Proc Natl Acad Sci U S A 100(26):15764-9 SGD PMID 14671320
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UW Stout/FA 2022 Glycerol Media
Introduction
Following the UW-Stout/Glycerol FA22 protocol, 5 knockout strains of yeast cell were tortured within a glycerol media solution.
Results
The following doubling times were calculated:
- Glycerol Trial 1: NA
- Negative Control Trial 1: 202 min
- Glycerol Trial 2: 689 min
- Negative Control Trial 2: 176 min
- Glycerol Trial 3: 2868 min
- Negative Control Trial 3: 264 min
Analysis/Conclusion
In the strains of yeast where the YCR095C gene was knocked out, a significant increase in doubling time can be seen. Disregarding trial 1 due to an unexpected collection error, the doubling times in the 2nd and 3rd trials, where the sample was kept in a 3% gliserol growth medium, showed significant results. In the second trial, the negative control had a doubling time of 176 while the glycerol sample had a doubling time of 689 min; this is an increase that is comparable to the pilot, where the doubling time doubled from the negative control to the glycerol sample. What we can conclude from this is that the samples in the glycerol media are only able to divide at a rate of about ½ to ⅓ of the rate of the glucose samples. Trial 3 shows a very exaggerated form of the data seen in Trial 2. This can be written up to error in preparing the samples, but the fact that the negative control for Trial 3 has a doubling time of 264 min while the one for the glycerol sample is 2868 min still shows that the cells have a much harder time dividing in the glycerol solution.
UW Stout/FA 2022 Bud Scars
Cells that had the gene YCR095C had an average of 2.12 scars per cell. Out of 100 cells counted, 212 bud scars were counted. The wild yeast BY4735 had an average of 2.46 bud scars per cell (100 cells counted, 246 bud scars). This indicates that the knocked-out gene slightly slowed down the reproduction rate of these cells.
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"picture does not include all cells that were counted"
