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Sample GSM843196 Query DataSets for GSM843196
Status Public on May 09, 2012
Title PPT 0h nodules biological rep 2
Sample type RNA
 
Source name 20 dpi nodules harvested from Medicago truncatula plants
Organism Medicago truncatula
Characteristics tissue: Root nodule
genotype: Jemalong A17
age: 20 days
agent: untreated
time: 0 hrs
Treatment protocol Nodulated plants (20 days post inoculation) were treated with a volume of the herbicide BASTA® corresponding to 0.25 mM of PPT. The herbicide was added to the nutrient solution of the aeroponic container. Root nodules were harvested just before the PPT treatment (control; PPT 0h), and at 4, 8 and 24 hours after PPT application (PPT 4h, PPT 8h, and PPT 24h) The root nodule were separated from roots at 4 ºC, pooled and immediately frozen in liquid nitrogen and stored at -80ºC.
Growth protocol Medicago truncatula Gaertn cv Jemalong genotype A17 seeds were surface-sterilized and scarified. Plants were grown aeroponically in a climate chamber (photosynthetic photon flux: 150 to 200 μmol m-2 s-1) at a 16 h light (22 °C) and 8 h dark (19 °C) regime. One month-old plants were inoculated with Sinorhizobium meliloti strain Rm1021 pXLGD4 RCR 2011(GMI51) under nitrogen limiting conditions.
Extracted molecule total RNA
Extraction protocol Root nodule samples were ground using a chilled mortal and pestle prior to RNA extractions. Total RNA extraction was performed via RNeasy kits (Qiagen) according to the manufacturer’s instructions. RNA preparations were quality-checked both via spectrophotometry (NanoDrop ND-1000) and via capillary electrophoresis in RNA Nano chips (Agilent Bioanalyzer), as recommended by the manufacturers.
Label biotin
Label protocol RNA was processed for use on Affymetrix (Santa Clara, CA, USA) GeneChip Medicago Genome Arrays, according to the manufacturer’s GeneChip 3’ IVT Express kit user manual. Briefly, 100 ng of total RNA with by a RIN number (Agilent 2100 Bioanalyzer, Agilent, Böblingen, Germany) of at least 8.5 containing spiked-in poly-A+ RNA controls was used in a reverse transcription reaction (GeneChip 3’ IVT Express Kit; Affymetrix) to generate first-strand cDNA. After secondstrand synthesis, double-stranded cDNA was used in a 16 h in vitro transcription (IVT) reaction to generate aRNA (GeneChip 3’ IVT Express Kit; Affymetrix). Size distribution of in vitro transcribed aRNA and fragmented aRNA, respectively, was assessed via an Agilent 2100 Bioanalyzer, using an RNA 6000 Nano Assay.
 
Hybridization protocol 12.5 µg of fragmented aRNA was used in a 250-µl hybridization cocktail containing added hybridization controls. 200 µl of mixture was hybridized on arrays for 16 h at 45°C. Standard post hybridization wash and double-stain protocols (FS450_0001; GeneChip HWS kit, Affymetrix) were used on an Affymetrix GeneChip Fluidics Station 450
Scan protocol GeneChips were scanned on an Affymetrix GeneChip scanner 3000 7G.
Description PPT 0.2
Mt_MtGeneChip0161_A072_jbecker_IGC_PP.CEL
Gene expression data from 20 dpi nodules before PPT treatment
Data processing CEL files of the 12 arrays were normalized to a baseline array with median CEL intensity by applying an Invariant Set Normalization Method available in DNA-Chip Analyzer 2010 (http://www.dchip.org, Cheng Li Lab, Harvard). Normalized CEL intensities of the arrays were used to obtain model-based gene expression indices based on a PM (Perfect Match)-only model. Subsequently log2 transformed expression data for the 50963 probe sets on the array representing Medicago truncatula transcripts were imported into Partek Genomics Suite 6.5.
 
Submission date Dec 05, 2011
Last update date May 09, 2012
Contact name Helena Carvalho
E-mail(s) mhcarval@ibmc.up.pt
URL http://www.ibmc.up.pt
Organization name Instituto de Biologia Molecular e Celular
Department MBNA
Street address Rua do Campo Alegre,823
City Porto
ZIP/Postal code 4150-180
Country Portugal
 
Platform ID GPL4652
Series (1)
GSE34155 Gene expression data from phosphinothricin (PPT) treated Medicago truncatula root nodules

Data table header descriptions
ID_REF
VALUE Log2 transformed expression values after model-based expression value computation in DNA-Chip Analyzer.
ABS_CALL

Data table
ID_REF VALUE ABS_CALL
AFFX-BioB-5_at 9.37 P
AFFX-BioB-M_at 9.52 P
AFFX-BioB-3_at 9.25 P
AFFX-BioC-5_at 10.3 P
AFFX-BioC-3_at 10.55 P
AFFX-BioDn-5_at 11.35 P
AFFX-BioDn-3_at 12.02 P
AFFX-CreX-5_at 13.35 P
AFFX-CreX-3_at 13.58 P
AFFX-DapX-5_at 7.13 P
AFFX-DapX-M_at 8.06 P
AFFX-DapX-3_at 8.32 P
AFFX-LysX-5_at 4.29 P
AFFX-LysX-M_at 5.11 P
AFFX-LysX-3_at 5.38 P
AFFX-PheX-5_at 5.57 P
AFFX-PheX-M_at 5.42 P
AFFX-PheX-3_at 6.17 P
AFFX-ThrX-5_at 5.01 P
AFFX-ThrX-M_at 5.9 P

Total number of rows: 61278

Table truncated, full table size 1486 Kbytes.




Supplementary file Size Download File type/resource
GSM843196.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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