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SRX7894906: GSM4407131: A33 exp6 rep2 [AT_an.A33.d204023]; Saccharomyces cerevisiae; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 4M spots, 197.9M bases, 113.7Mb downloads

Submitted by: NCBI (GEO)
Study: The environmental stress response causes ribosome loss in aneuploid yeast cells.
show Abstracthide Abstract
Aneuploidy, a condition characterized by whole chromosome gains and losses, is often associated with significant cellular stress and decreased fitness. However, whether and how cells respond to the aneuploid state has remained controversial. In aneuploid budding yeast, two opposing gene expression patterns have been reported: an environmental stress response (ESR) and a “common aneuploidy gene-expression” (CAGE) signature, in which many ESR genes are oppositely regulated. Here, we investigate and bring clarity to this controversy. We show that the CAGE signature is not an aneuploidy-specific gene expression signature but is the result of euploid control cells, but not aneuploid cells, having grown into stationary phase. Because growth into stationary phase is amongst the strongest inducers of the ESR, the ESR in aneuploid cells was masked when stationary phase euploid cells were used for normalization in transcriptomic studies. When exponentially growing euploid cells are used in gene expression comparisons with aneuploid cells, the CAGE signature is no longer evident in aneuploid cells. Instead, aneuploid cells are found to exhibit the ESR. We further show that the ESR causes a selective loss of ribosomes in aneuploid cells, providing an explanation for the decreased cellular density in aneuploid cells. We conclude that aneuploid budding yeast cells mount the ESR, rather than a CAGE signature, in response to aneuploidy-induced cellular stresses that results in selective ribosome loss. Overall design: Examination of gene expression signatures in euploid and aneuploid yeast strains under different growth conditions.
Sample: A33 exp6 rep2 [AT_an.A33.d204023]
SAMN14354941 • SRS6303998 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: 3-5 mL samples of culture were taken, spun down at 3000rpm for 5 minutes, washed with 1 mL DEPC water, and transferred to a 2 mL RNase-free screw-cap tube. Samples were spun again at 8000rpm for 3 minutes, and supernatant was aspirated. Cells were snap frozen with liquid nitrogen and stored at -80C. RNA samples were prepared with RNeasy mini kit from Qiagen and treated with DNase on-column treatment (RNase-free) from Qiagen. Illumina Truseq or KAPA
Experiment attributes:
GEO Accession: GSM4407131
Links:
Runs: 1 run, 4M spots, 197.9M bases, 113.7Mb
Run# of Spots# of BasesSizePublished
SRR112892333,957,325197.9M113.7Mb2020-06-16

ID:
10326260

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