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Sample GSM307246 Query DataSets for GSM307246
Status Public on Oct 01, 2008
Title DNA damage decay profile, t=40min
Sample type RNA
 
Source name MMS treatment, 40 min following transcription inhibition
Organism Saccharomyces cerevisiae
Characteristics strain Y262
Treatment protocol In the oxidative stress and DNA damage experiments, cells were treated with 0.3mM H2O2 or 0.1% MMS, 25 or 40 minutes prior to transcription inhibition. At time point 0, the temperature of the culture was raised to 37 degrees by adding an equal amount of medium prewarmed to 49 degrees. This step inactivated the temperature-sensitive RNA polymerase II and therefore stopped transcription. Following transcription inhibition, 10 samples were taken for each time course (0, 5 min, 10 min, 15 min, 20 min, 30 min, 40 min, 50 min, 60 min) and a technical replicate of time point zero. In the second reference decay profile, the three last time points (40 min, 50 min, and 60 min) turned out to be outliers, and thus were not used and not submitted.
Growth protocol Yeast strain Y262 (carrying a temperature-sensitive mutation in RNA polymerase II) was grown in YPD to mid-log phase in 26 degrees.
Extracted molecule polyA RNA
Extraction protocol Total RNA was extracted using MasterPureā„¢ (EPICENTER Biotechnologies).
Label biotin
Label protocol cDNA was prepared using poly(T) primers, labeled cRNA was prepared using the GeneChip system according to manufacturer instructions.
 
Hybridization protocol GeneChip system according to manufacturer instructions.
Scan protocol GeneChip system according to manufacturer instructions.
Description Decay profile following DNA damage, t=40 min
Data processing RMA algorithm followed by normalization using spiked-in RNA as explained in detail in the supplementary of the paper (Shalem et al.).
 
Submission date Jul 23, 2008
Last update date Jul 24, 2008
Contact name Ophir Shalem
E-mail(s) ophir.shalem@weizmann.ac.il
Organization name Weizmann Inst.
Street address Hertzel
City Rehovot
ZIP/Postal code 76100
Country Israel
 
Platform ID GPL2529
Series (2)
GSE12221 Decay profiles of Saccharomyces cerevisiae mRNAs following oxidative stress and DNA damage
GSE12222 Transient transcriptional responses to stress are generated by opposing effects of mRNA production and degradation

Data table header descriptions
ID_REF
VALUE Signal intensity calculated by RMA followed by normalization using spiked-in RNA
RATIO Normalized decay profile; the whole time course is divided by the mean of the two replicates at time point zero. Data is not in log scale.

Data table
ID_REF VALUE RATIO
1769308_at 10.93559643 0.426054943
1769311_at 11.48506665 0.152357099
1769312_at 12.14914285 0.694251248
1769313_at 11.5961129 0.510096859
1769314_at 12.51908863 0.447941244
1769317_at 9.059329776 0.290530202
1769319_at 12.69597088 0.489169194
1769320_at 10.13231336 0.477173053
1769321_at 14.08723128 0.556057237
1769322_s_at 9.582051575 0.360043897
1769323_at 12.57911524 0.662319791
1769324_at 9.445231639 0.30584605
1769325_at 10.7630806 0.747169725
1769329_at 11.49466782 0.414574927
1769331_at 11.10125267 0.25939828
1769333_at 9.80275291 0.693164977
1769335_at 11.68816579 0.249005524
1769336_at 9.262515527 0.299428641
1769338_at 7.615562961 0.131009434
1769339_at 11.36295881 0.341683975

Total number of rows: 5900

Table truncated, full table size 202 Kbytes.




Supplementary file Size Download File type/resource
GSM307246.CEL.gz 1019.6 Kb (ftp)(http) CEL
Processed data included within Sample table

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