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Sample GSM476033 Query DataSets for GSM476033
Status Public on Apr 01, 2010
Title Roots: Champagne acclimated 5 days
Sample type RNA
 
Channel 1
Source name roots of Champagne acclimated 5 days
Organism Pisum sativum
Characteristics variety: Champagne
tissue: roots
Biomaterial provider UMR1281 USTL INRA
Treatment protocol Low temperature treatment 5 days
Growth protocol Plants were grown under greenhouse conditions 19°C day/12°C night, 10h light/day and 300µmol/m²s (phase of nursery) following of 5 days of culture to 10°C day/2°C night 10h light/day and 250µmol/m²s (phase of acclimation).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using a Tri reagent kit (Euromedex). RNA quantification was done by capillary electrophoresis (Experion, Biorad).
Label CY5,CY3
Label protocol Twenty-five μg of total RNA were used for each experiment. Reverse transcription and fluorochrome incorporation were performed in a MJ PTC-200 Peltier Thermal Cycler, using oligo-dT (Roche), the Superscript II Kit (Invitrogen) and CY3- and CY5-labelled d-CTP (Amersham). The QIAquick PCR Purification Kit (Qiagen) was used for target purification.
 
Channel 2
Source name roots of Champagne without treatment (d0)
Organism Pisum sativum
Characteristics variety: Champagne
tissue: roots
Biomaterial provider UMR1281 USTL INRA
Treatment protocol Without temperature treatment (d0)
Growth protocol Plants were grown under greenhouse conditions 19°C day/12°C night, 10h light/day and 300µmol/m²s (phase of nursery).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using a Tri reagent kit (Euromedex). RNA quantification was done by capillary electrophoresis (Experion, Biorad).
Label CY3,CY5
Label protocol Twenty-five μg of total RNA were used for each experiment. Reverse transcription and fluorochrome incorporation were performed in a MJ PTC-200 Peltier Thermal Cycler, using oligo-dT (Roche), the Superscript II Kit (Invitrogen) and CY3- and CY5-labelled d-CTP (Amersham). The QIAquick PCR Purification Kit (Qiagen) was used for target purification.
 
 
Hybridization protocol 14-18 h hybridization (DigEasy hybridization buffer; Roche) at 42°C in a Corning chamber. Slides were washed successively in 4x, 2x (with SDS 0.1x), 0.2x, and 0.1x SSC.
Scan protocol Images were acquired with a GenePix4000B scanner (Molecular Devices, Sunnyvale, CA, USA)
Description Images were analyzed with GenePix Pro 6.0 software (Axon).
Data processing Artefactual, saturated, or low-signal spots were eliminated from the analysis and the background subtracted median intensities used for calculations. For each slide a global lowess followed by a print-tip median normalization was performed using R (http://cran.r-project.org/) packages as implemented in Goulphar (Lemoine et al. 2006). In order to exclude possible dye effects, all probes exhibiting an opposite behaviour in the swapped-dye experiment were eliminated from the final analysis. To identify genes displaying a change in expression over repetitions, a script utilizing libraries functions in R with a false discovery rate (FDR) less than 5% was used for all experimental conditions. Only genes with smooth expression profiles were retained. The SAM (Tusher et al. 2001) was used to identify differentially expressed genes over different conditions and log2(ratio) ≥1 and ≤ -1 were used for filtering gene expression profiles. Three biological replicates were mixed and used for two individual hybridizations.
 
Submission date Nov 26, 2009
Last update date Dec 10, 2009
Contact name Lucau Anca
E-mail(s) Anca.Lucau@univ-lille1.fr
Phone +33320434428
URL http://www.univ-lille1.fr/pdv/labo/microarray.htm
Organization name UMR USTL / INRA 1281
Department Stress Abiotiques et Différenciation des Végétaux Cultivés
Lab Adaptation au froid du pois protéagineux
Street address Cité Scientifique SN2/302
City Villeneuve d'Ascq
ZIP/Postal code 59000
Country France
 
Platform ID GPL8288
Series (1)
GSE19209 Cold acclimation in pea

Data table header descriptions
ID_REF
VALUE log2-transformed Lowess ratio representing treated/untreated (d0)

Data table
ID_REF VALUE
Alien1 null
Alien10 null
Alien2 null
Alien3 null
Alien4 null
Alien5 null
Alien6 null
Alien7 null
Alien8 null
Alien9 null
BAR -0.1480
empty null
GFP -0.3747
GUS -1.0664
HPH -0.0514
LUC -0.2345
NCPS01 -0.0847
NCPS02 null
NCPS03 -0.6215
NCPS04 null

Total number of rows: 5278

Table truncated, full table size 93 Kbytes.




Supplementary file Size Download File type/resource
GSM476033-CY3_Roots_Champagne_day_5_vs_CY5-Champagne_day_0-repetition2.gpr.gz 1.3 Mb (ftp)(http) GPR
GSM476033-CY5_Roots_Champagne_day_5_vs_CY3-Champagne_day_0-repetition1.gpr.gz 1.3 Mb (ftp)(http) GPR
Processed data included within Sample table

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