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Sample GSM352208 Query DataSets for GSM352208
Status Public on Jun 22, 2009
Title CJD21/PMK + Benomyl (expt 3)
Sample type RNA
 
Source name CAP1-deficient strain, benomyl-treated
Organism Candida albicans
Characteristics strain: CJD21/PMK
experimental treatment: benomyl, 25 mcg/ml, 30min
Biomaterial provider Martine Raymond
Treatment protocol Cultures were grown to saturation overnight in YPD at 30deg Celsius with agitation. Optical density was then adjusted to 0.2, and cultures were grown an additional 3hrs as before in YPD. Benomyl was then added to the culture to a final concentration of 25 mcg/ml, and cells were incubated for 30min as before.
Extracted molecule total RNA
Extraction protocol Cells were collected by centrifugation, and cell pellets were stored at -80 deg Celsius at least 30min until RNA was isolated. TOtal RNA was isolated using the hot phenol method.
Label biotin
Label protocol First and second strand cDNA was synthesized from 15 μg total RNA using the SuperScript Double-Stranded cDNA Synthesis Kit (Invitrogen) and oligo-dT24-T7 primer (PrOligo) according to the manufacturer's instructions. cRNA was synthesized and labelled with biotinylated UTP and CTP by in vitro transcription using the T7 promoter-coupled double stranded cDNA as template and the Bioarray HighYield RNA Transcript Labelling Kit (ENZO Diagnostics). Double stranded cDNA synthesized from the previous steps was washed twice with 70% ethanol and suspended in 22 μl of RNase-free water. The cDNA was incubated as recommended with reaction buffer, biotin-labeled ribonucleotides, dithtiothreitol, RNase inhibitor mix, and T7 RNA polymerase for 5 h at 37°C. The labeled cRNA was separated from unincorporated ribonucleotides with a CHROMA SPIN-100 column (Clontech) and ethanol precipitated at −20°C overnight.
 
Hybridization protocol The cRNA pellet was suspended in 10 μl of RNase-free water and 10 μg was fragmented at 95°C for 35 min in 200 mM Tris-acetate (pH 8.1), 500 mM potassium acetate, 150 mM magnesium acetate. The fragmented cRNA was hybridized for 16 h at 45°C to C. albicans NimbleExpress GeneChip arrays (Affymetrix). Arrays were washed at 25°C with 6 × SSPE, 0.01% Tween 20 followed by a stringent wash at 50°C with 100 mM MES, 0.1 M NaCl, 0.01% Tween 20. Hybridizations and washes employed the Affymetrix Fluidics Station 450 using their standard EukGE-WS2v5 protocol. The arrays were then stained with phycoerythrein-conjugated streptavidin (Molecular Probes).
Scan protocol The fluorescence intensities were determined using the GCS 3000 high-resolution confocal laser scanner (Affymetrix). The scanned images were analyzed using software resident in GeneChip Operating System v2.0 (GCOS; Affymetrix). Sample loading and variations in staining were standardized by scaling the average of the fluorescent intensities of all genes on an array to a constant target intensity of 250. The signal intensity for each gene was calculated as the average intensity difference, represented by [Σ(PM – MM)/(number of probe pairs)], where PM and MM denote perfect-match and mismatch probes, respectively.
Description first-generation custom C. albicans Affymetrix chips manufactured by NimbleGen.
Data processing The scaled gene expression values from GCOS software were imported into GeneSpring 7.2 software (Agilent Technologies) for preprocessing and data analysis. Probesets were deleted from subsequent analysis if they were called absent by the Affymetrix criterion and displayed an absolute value below 20 in all experiments. The expression value of each gene was normalized to the median expression of all genes in each chip as well as the median expression for that gene across all chips in the study. Pairwise comparison of gene expression was performed for each matched experiment.
 
Submission date Dec 17, 2008
Last update date Jun 04, 2010
Contact name Katherine S Barker
E-mail(s) [email protected]
Organization name University of Tennessee Health Science Center
Department Clinical Pharmacy
Lab David Rogers laboratory
Street address 881 Madison Avenue, Room 305
City Memphis
State/province TN
ZIP/Postal code 38163
Country USA
 
Platform ID GPL5723
Series (1)
GSE14258 Identification of the Candida albicans CAP1 regulon

Data table header descriptions
ID_REF
VALUE signal intensity value
DETECTION P-VALUE detection p-value

Data table
ID_REF VALUE DETECTION P-VALUE
AFFX-BioB-5_at 66.2 0.000127
AFFX-BioB-M_at 53.4 0.000127
AFFX-BioB-3_at 43 0.000662
AFFX-BioC-5_at 115 0.000081
AFFX-BioC-3_at 91.8 0.000127
AFFX-BioDn-5_at 149.4 0.000044
AFFX-BioDn-3_at 596.5 0.000044
AFFX-CreX-5_at 1627.9 0.00007
AFFX-CreX-3_at 1337.2 0.000044
AFFX-DapX-5_at 3.5 0.300606
AFFX-DapX-M_at 6.3 0.300606
AFFX-DapX-3_at 1 0.699394
AFFX-LysX-5_at 1.8 0.39692
AFFX-LysX-M_at 5.6 0.368438
AFFX-LysX-3_at 3.5 0.544587
AFFX-PheX-5_at 0.9 0.843268
AFFX-PheX-M_at 4.4 0.327079
AFFX-PheX-3_at 4.4 0.60308
AFFX-ThrX-5_at 1.3 0.772364
AFFX-ThrX-M_at 1.3 0.712257

Total number of rows: 10781

Table truncated, full table size 291 Kbytes.




Supplementary file Size Download File type/resource
GSM352208.CEL.gz 2.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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