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| Status |
Public on Aug 17, 2020 |
| Title |
Aneuploidy-induced proteotoxic stress can be effectively tolerated without dosage compensation, genetic mutations or stress responses |
| Organism |
Saccharomyces cerevisiae |
| Experiment type |
Expression profiling by high throughput sequencing
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| Summary |
The protein homeostasis (proteostasis) network maintains balanced protein synthesis, folding, transport and degradation within a cell. Because failure to maintain proteostasis is associated with aging and disease, a concerted effort has been placed on studying how the proteostasis network responds to various stresses. Typically, this is accomplished using ectopic overexpression of well-characterized, model misfolded protein substrates; however, how cells tolerate large-scale, diverse burden to the proteostasis network is not understood. Aneuploidy, the state of imbalanced chromosome content, adversely affects the proteostasis network by dysregulating the expression of hundreds of proteins simultaneously. Using aneuploid yeast cells as a model, we address what compensatory adjustments enable cells to tolerate large-scale, diverse challenges to the proteostasis network. Here we show adapted aneuploid Saccharomyces cerevisiae strains that exhibit robust growth and enhanced stress tolerance associated with enhancement of translation, folding, and quality control systems without genetic changes or activation of canonical stress response pathways.
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| Overall design |
Total mRNA and ribosome-protected footprints were analyzed by RNA-Seq.total RNA and RPFs were extracted following manufacturer's instructions from the TruSeq Ribo Profile kit (formerly ARTseq) from Illumina Libraries were prepared with the TruSeq Ribo Profile kit (formerly ARTseq) from Illumina, according to manufacturer's instructions. In one run conducted in 2015, WT (RLY2626), D2 (NVY1) and D1/2 (NVY2) were run together (no biological replicates). Another run was conducted in 2017 in which one biological replicate each of D1/2/8 (NVY3) and D13 (KLY196), and two biological replicates each of D1/2/8/11(KLY193), D1/8 (KLY194) and D13 (KLY195) were run.
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| Contributor(s) |
Larrimore KE, Barattin-Voynova NS, Reid DW |
| Citation(s) |
32900371 |
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| Submission date |
Nov 20, 2019 |
| Last update date |
Sep 21, 2020 |
| Contact name |
Katherine Larrimore |
| Organization name |
Temasek Life Sciences Laboratory
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| Department |
Cell Biology
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| Street address |
1 Research Link
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| City |
Singapore |
| ZIP/Postal code |
117604 |
| Country |
Singapore |
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| Platforms (1) |
| GPL13821 |
Illumina HiSeq 2000 (Saccharomyces cerevisiae) |
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| Samples (24)
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| Relations |
| BioProject |
PRJNA590714 |
| SRA |
SRP230795 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE140733_RAW.tar |
1.3 Mb |
(http)(custom) |
TAR (of TXT) |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data provided as supplementary file |
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