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Sample GSM1543562 Query DataSets for GSM1543562
Status Public on Jun 30, 2016
Title C24 WT at 48h after chilling rep1
Sample type RNA
 
Source name Col WT, chilling treatment for 48h, replicate 1
Organism Arabidopsis thaliana
Characteristics tissue: leaf
genotype/variation: wildtype
ecotype: Col
Treatment protocol Two-week-old seedlings were transferred to 4 degree for 0, 3, and 48 h. Plant materials were then collected for RNA extraction.
Growth protocol Arabidopsis seeds of rdm4 mutant and Col WT were sown in MS plates and grown at 23/18°C in a growth room with a 16-h light/8-h dark cycle at 150 μmol m-2s-1 and 70% relative humidity
Extracted molecule total RNA
Extraction protocol Total RNA was extracted and purified from leaves of at least 30 seedlings per plate using QIAGEN-RNeasy Mini Kit (Qiagen, Valencia, CA, USA) according to guidelines specified by the manufacturer. Two biological replicates were prepared for each combination. RNA was quantified using a Nanodrop-ND 8000 spectrophotometer (Thermo Fisher Scientific) and RNA quality was assessed by agarose gel analysis and using a 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA) according to the manufacturer’s protocol. Samples with the RNA integrity number of 7.5 and above were chosen for further analysis.
Label biotin
Label protocol Total RNA from rdm4 and C24 WT seedlings with or without cold treatment (0, 3 or 48 h) was and used to make biotin-labeled cRNA targets. Two biological replicates from different growth chambers were prepared for each combination of ecotype and cold treatment.
 
Hybridization protocol Fragmented cRNAs (15 μg) were hybridized to the 24K GeneChip Arabidopsis ATH1 Genome Array (Affymetrix) according to the manufacturer’s instructions.
Scan protocol The arrays were scanned with a GeneChip® Scanner 3000 (Affymetrix), and raw image files were converted to probe set data (*.CEL files), using the Affymetrix GeneChip® Operating Software according to the manufacturer’s instructions.
Description Gene expression after 48h of chilling treatment
Data processing All of the raw data (*.CEL files) were then analyzed using the affylmGUI package in the statistical computing environment R
All genes with a P value < 0.05 and a fold-change > 2 were chosen for further analysis
 
Submission date Nov 12, 2014
Last update date Jun 30, 2016
Contact name Zhulong Chan
E-mail(s) zhulongch@wbgcas.cn
Organization name Chinese Academy of Sciences
Department Wuhan Botanic Garden
Street address Moshan, Wuchang District
City Wuhan, Hubei Province
ZIP/Postal code 430074
Country China
 
Platform ID GPL198
Series (2)
GSE63185 RNA-DIRECTED DNA METHYLATION 4 modulates cold stress resistance in Arabidopsis through the C-REPEAT-BINDING FACTOR-mediated pathway [Affymetrix]
GSE63186 RNA-DIRECTED DNA METHYLATION 4 modulates cold stress resistance in Arabidopsis through the C-REPEAT-BINDING FACTOR-mediated pathway

Data table header descriptions
ID_REF
VALUE RMA

Data table
ID_REF VALUE
244901_at 4.671036498
244902_at 4.722788825
244903_at 6.659297655
244904_at 6.386580535
244905_at 4.482647109
244906_at 6.28602561
244907_at 3.752922088
244908_at 3.909404316
244909_at 4.065974324
244910_s_at 3.810217226
244911_at 3.464500325
244912_at 9.643974808
244913_at 4.591782082
244914_at 3.459776632
244915_s_at 4.272768328
244916_at 4.276550742
244917_at 3.832575658
244918_at 3.472521163
244919_at 4.579823734
244920_s_at 5.352483113

Total number of rows: 22810

Table truncated, full table size 490 Kbytes.




Supplementary file Size Download File type/resource
GSM1543562_03_C24_48h1_ATH1-121501_.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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