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Links from GEO DataSets

Items: 8

1.

Expression profile of Yeast Frataxin Mutants

(Submitter supplied) Yeast Frataxin Homologue 1 has been involved in oxidative stress and iron-sulfur biogenesis within the mitochondria. We have investigated the expression profile of conditional Yfh1 mutants. Yfh1 depletion leads to activation of iron uptake and repression
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL10039
6 Samples
Download data: GPR
Series
Accession:
GSE44871
ID:
200044871
2.

GRX5, PET117 and MLP1 yeast mutants

(Submitter supplied) Transcriptome comparisons between grx5, pet117 and mlp1 mutants. All of them are referenced to the same parental wild type sample using three independent samples and three independent nylon macroarrays. Each replicate pair (wt/mutant), hybridized on the same membrane, was normalized by lowess method. z-tests were performed to evaluate differential gene expression. Keywords = yeast Keywords = GRX5 Keywords = PET117 Keywords: other
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Dataset:
GDS529
Platform:
GPL772
12 Samples
Download data
Series
Accession:
GSE910
ID:
200000910
3.
Full record GDS529

Oxidative stress and glutaredoxin 5-deficient mutant

Transcriptome analysis of glutaredoxin 5-deficient (grx5) mutant, a model for continuous moderate oxidative stress. Respiratory petite (pet117) mutants and wild type also examined.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array, count, 3 strain sets
Platform:
GPL772
Series:
GSE910
9 Samples
Download data
DataSet
Accession:
GDS529
ID:
529
4.

Deficiency of the RNA-binding protein Cth2 extends yeast replicative lifespan by alleviating its repressive effects on mitochondrial function

(Submitter supplied) Iron dyshomeostasis contributes to aging, but little information is available about the molecular mechanisms. Here, we provide evidence that, in Saccharomyces cerevisiae, aging is associated with altered expression of genes involved in iron homeostasis. We further demonstrate that defects in the conserved mRNA-binding protein Cth2, which controls stability and translation of mRNAs encoding iron-containing proteins, increase lifespan by alleviating its repressive effects on mitochondrial function. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13821
15 Samples
Download data: TXT
Series
Accession:
GSE189306
ID:
200189306
5.

Cooperation of two mRNA-binding proteins drives metabolic adaptation to iron deficiency

(Submitter supplied) Expression of the yeast Cth2 protein stimulates degradation of mRNAs encoding proteins with Fe-dependent functions in metabolism, in iron storage and in other cellular processes. We demonstrate that in response to Fe deprivation, the Cth2-homologue, Cth1, stimulates specific degradation of mRNAs involved in mitochondrially localized activities that include respiration and amino acid biosynthesis. Furthermore, yeast cells grown under Fe deprivation accumulate mRNAs encoding proteins that function in glucose metabolism. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL90
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE11236
ID:
200011236
6.

Chemical potentiator of copper-accumulation and -toxicity: Probing iron- regulons of Saccharomyces cerevisiae

(Submitter supplied) RNA-seq was used to assess mRNA transcript abundance in wild type and fra2Δ S. cerevisiae (BY4741) cells treated with 2-(6-benzyl-2-pyridyl)quinazoline (BPQ) and CuSO4. BPQ potentiates copper toxicity and in yeast, in common with other organisms, a major cause of copper toxicity is damage of iron-sulphur clusters. Iron sensing within yeast relies on mitochondrial iron-sulphur cluster biosynthesis and therefore treatment with BPQ and copper can be used to mimic iron deficiency. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17342
18 Samples
Download data: TXT
Series
Accession:
GSE54045
ID:
200054045
7.

The metabolic responce to iron deficiency in Saccharomyces cerevisiae

(Submitter supplied) Iron is an essential cofactor for enzymes involved in numerous cellular processes. We analyzed the metabolomes and transcriptomes of yeast grown in iron-rich and iron-poor media to determine which biosynthetic processes are altered when iron availability falls.
Organism:
Schizosaccharomyces pombe; Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL2529
8 Samples
Download data: CEL
Series
Accession:
GSE19016
ID:
200019016
8.

Iron uptake experiments in yeast

(Submitter supplied) The budding yeast S. cerevisiae responds to depletion of iron in the environment by activating Aft1p, the major iron-dependent transcription factor, and by transcribing systems involved in the uptake of iron. Here we have studied the transcriptional response to iron deprivation, and have identified new Aft1p target genes. We find that other metabolic pathways are regulated by iron: biotin uptake and biosynthesis, nitrogen assimilation, and purine biosynthesis. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platforms:
GPL58 GPL59 GPL64
6 Samples
Download data
Series
Accession:
GSE4196
ID:
200004196
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