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Series GSE20566 Query DataSets for GSE20566
Status Public on Mar 02, 2010
Title Glucose uptake is required for glucose-stimulated transcriptional response in Saccharomyces cerevisiae
Platform organisms Schizosaccharomyces pombe; Saccharomyces cerevisiae
Sample organism Saccharomyces cerevisiae
Experiment type Expression profiling by array
Summary Saccharomyces cerevisiae developed elegant mechanisms to monitor nutrient availability and trigger adaptative responses to nutrient deficiency. Nutrient sensing requires close coordination of cell surface sensors with intracellular mechanisms. This yeast senses the presence of glucose by two modified hexose transporters, Rgt2 and Snf3 (regulating expression of genes encoding hexose transporters) and the G-protein coupled receptor Gpr1 (modulating Protein Kinase A (PKA) activity).. It has been difficult to differentiate between cellular responses mediated by cell surface and intracellular sensors, respectively. Using a strain that is devoid of glucose uptake, we show that the mere presence of glucose does not elicit any glucose-dependent transcriptional responses. This indicates that signals generated by surface sensors are not sufficient to mediate glucose-dependent transcriptional responses. Instead, intracellular glucose or metabolites derived from it are required for transcriptional changes associated with glucose exposure.
We used microarrays from biological triplicate samples to measure the global transcriptional response to sudden addition of glucose to yeast cells growing at steady state on ethanol. The experiment was conducted using a strain that is devoid of glucose uptake and compared with an isogenic strain.
 
Overall design The CEN.PK strain was used in this research. A strain with all known hexose transporters deleted (Null strain) was compared with an isogenic reference. The two strains were grown in a chemostat (D = 0.1 h-1) using ethanol as the carbon source. Transcriptional responses between the strains were measured in biological triplicates at steady state and then pulsed with glucose at time t = 0. Transcriptional response was measured again after t = 20 min to determine changes in gene expression chanes only in response to the presence of glucose.
 
Contributor(s) Vemuri GN
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Submission date Mar 01, 2010
Last update date Feb 21, 2017
Contact name Goutham N Vemuri
E-mail(s) goutham@chalmers.se
Phone +46 031 772 3882
Fax +46 031 772 3801
Organization name Chalmers University of Technology
Department Chemical and Biological Engineering
Lab Systems Biology
Street address Kemivagen 10
City Göteborg
ZIP/Postal code 412 96
Country Sweden
 
Platforms (1)
GPL2529 [Yeast_2] Affymetrix Yeast Genome 2.0 Array
Samples (12)
GSM516818 REF0_1
GSM516819 REF0_2
GSM516820 REF0_3
Relations
BioProject PRJNA125219

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE20566_RAW.tar 12.1 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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