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Sample GSM244911 Query DataSets for GSM244911
Status Public on Nov 26, 2007
Title 40_SLO.M2W3.CEL, Experimental replicate 3
Sample type RNA
 
Source name Soybean cultivar SLOAN - Mock Inoculated (Inoculated with water + agar): 48 hours post inoculation
Organism Glycine max
Characteristics cultivar - SLOAN
Tissue/Cell Type: Soybean root/hypocotyls - P.sojae mycelium from minimal medium
total Soybean RNA Plus 1 % P.sojae RNA added
Treatment protocol Inoculation assays were performed using the slant board technique (Olah and Schmitthenner, 1985).[ Briefly, 7-day-old soybean seedlings were thoroughly rinsed under tap water and placed in an inoculation tray (10 plants per tray, 3 trays per inoculation replication). The plants were wounded at 2 cm below the beginning of the root zone by scraping the epidermis with a scalpel and then inoculated with a mycelial slurry from a 7-day-old culture or agar alone. Samples of root tissues were collected at 3 and 5 days post inoculation (dpi) from 7.5 mm below and above the lesion margin from each seedling with characteristic lesions. For the mock-inoculated plants, tissue sections were taken 7.5 mm below and above the position corresponding to the average lesion length measured from the inoculated samples. The lesion length (mm) from the inoculation point up to the edge of the lesion margin was also measured 3 and 5 dpi. For each experimental replication, 2 replicates of 30 seedlings per condition were inoculated and harvested separately. All the plants for an experiment were grown in the same environmental growth chamber (Chagrin Falls, Ohio; Model M-48 with TC2 microcontroller unit) with day and night temperatures settings of 27C and 21C and relative humidity averaging 75 to 90%.
Growth protocol Soybean plants were grown in growth chambers and later transferred to trays with clothes soaked in water
Extracted molecule total RNA
Extraction protocol QIAGEN RNeasy Kit : As recommended by manufacturer
Label biotin
Label protocol The RNA samples isolated from each of the two inoculation replications were pooled in equal amounts before subjecting to microarray assay. RNA samples from mock inoculated tissue contain 0.03125-4% spike-in RNA from Phytophthora sojae mycellium grown in liquid sucrose-salts medium , depending upon resistance level and sampling time. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from total RNA. RNA is is first reverse transcribed using a T7-Oligo(dT) Promoter Primer in the first-strand cDNA synthesis reaction. Following RNase H-mediated second-strand cDNA synthesis, the double-stranded cDNA is purified and serves as a template in the subsequent in vitro transcription (IVT) reaction. The IVT reaction is carried out in the presence of T7 RNA Polymerase and a biotinylated nucleotide analog/ribonucleotide mix for complementary RNA (cRNA) amplification and biotin labeling. The biotinylated cRNA targets are then cleaned up, fragmented, and hybridized to GeneChip expression arrays(Affymetrix Technical manual - 2004)
 
Hybridization protocol hybridization cocktail is prepared, including the fragmented target, probe array controls, BSA, and herring sperm DNA. It is then hybridized to the probe array during a 16-hour incubation(Affymetrix technical manual - 2004)
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneChip Scanner 3000
Description SLOAN - Mock inoculated; 48 hrs; ExpRep3
Data was collected from the hypocotyl regions of Soybean plants at different time points
Data processing The data were analyzed with RMA suite from R package version 2.4.0. Background correction was using RMA followed by quantile normalization and data was summarized using median polish method
 
Submission date Nov 26, 2007
Last update date Aug 14, 2011
Contact name sucheta Tripathy
E-mail(s) sutripa@vbi.vt.edu
Phone 5402318138
Organization name Virginia Tech
Department Virginia Bioinformatics Institute
Lab Tyler lab
Street address 1, Washington street
City Blacksburg
State/province VA
ZIP/Postal code 24061
Country USA
 
Platform ID GPL4592
Series (1)
GSE9687 Expression patterns in time and space during P.sojae infection of soybean cultivars differing in quantitative resistance

Data table header descriptions
ID_REF Gene IDs
VALUE RMA processed value

Data table
ID_REF VALUE
AFFX-BioB-3_at 6.46024409810711
AFFX-BioB-5_at 6.70266073702572
AFFX-BioB-M_at 6.65147169886279
AFFX-BioC-3_at 7.70018235168107
AFFX-BioC-5_at 8.03646502336775
AFFX-BioDn-3_at 10.5281345674523
AFFX-BioDn-5_at 9.33491173422986
AFFX-CreX-3_at 12.6719127855064
AFFX-CreX-5_at 12.3220166448622
AFFX-DapX-3_at 2.91116865127719
AFFX-DapX-5_at 2.8721002583725
AFFX-DapX-M_at 2.84718282969833
AFFX-Gm_18SrRNA_at 9.02852153751926
AFFX-Gm_Actin_3_at 9.99209132959016
AFFX-Gm_Actin_5_at 5.02402202107877
AFFX-Gm_Actin_M_at 9.0078504815618
AFFX-Gm_GlutTrans_3_r_at 8.86302728444337
AFFX-Gm_GlutTrans_5_s_at 9.70994867694042
AFFX-Gm_GlutTrans_M_at 7.88939131594177
AFFX-Gm_P450_3_s_at 12.5332907210828

Total number of rows: 61170

Table truncated, full table size 2240 Kbytes.




Supplementary file Size Download File type/resource
GSM244911.CEL.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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