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Sample GSM947264 Query DataSets for GSM947264
Status Public on Nov 28, 2012
Title 996-P-2hr-2
Sample type RNA
 
Source name rice spikelets of developmental stage7-9,2hr after 40 degree centigrade,replicate 2
Organism Oryza sativa
Characteristics cultivar: Heat-tolerant rice cultivar 996
developmental stage: phase 7-9 of panicle development with half length of mature spikelets
tissue: Young spikelets with the phase 7-9 at the middle of main panicles
stress: heat shock
time: 2hr
Treatment protocol The proper rice plants transplanted into pots were moved in a growth chamber (Binder, Tuttlingen, Germany) under the condition of 32°C with 80% humidity at day, and 28°C with 80% relative humidity at night for one day, and then at 40°C with 80% relative humidity and 600 μmol m-2 s-1 of photosynthetically active radiation for 8hr.
Growth protocol Heat-tolerant rice cultivar 996 was cultivated in the field until phase 7-9 of panicle development with half length of mature spikelets.
Extracted molecule total RNA
Extraction protocol Young spikelets with the phase 7-9 at the middle of main panicles were collected at the time point of 0min (as control), 20min, 1hr, 2hr, 4hr, and 8hr, respectively, after heat treatment, and frozen in liquid nitrogen immediately, and stored at -80°C for microarray hybridization.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 2μg RNA using the One-Color Low RNA Input Linear Amplification PLUS kit (Agilent) according to the manufacturer's instructions, followed by QIAGEN RNeasy Mini Kit (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 875 ng of Cy3-labelled cRNA was fragmented at 60°C for 30 minutes in a reaction volume of 55μl containing 25x Agilent fragmentation buffer and 10x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 55μl of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Whole Rice Genome Oligo Microarrays (015241) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried immediately by brief centrifugation.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2565BA) using one color scan setting for 4x44k array slides (Scan Area 61x21.6 mm, Scan resolution 5μm, Dye channel is set to Green and Green PMT is set to 100% and 10%, respectively), and the scan data with 100% and 10% PMT were merged automatically.
Description Gene expression of rice spikelets of developmental stage7-9,2hr after 40 degree centigrade
rice spikelets of developmental stage7-9 at the middle of main panicle
Data processing The above hybridization signal data files in text format from the Feature Extraction Software were imported into GeneSpring GX (Agilent Technologies). The data were marked with specific flag such as P, A, M (representing detected, not detected and compromised, respectively) using the default parameter and algorithm, and then normalized by Quantile algorithm followed by the process of baseline to median of all samples. The normalized data from two replicates of each sample were log2 transformed, and the correlation coefficient of replicates was determined through hierarchical clustering using complete linkage algorithm as implemented TIGR MeV version 4.0.
 
Submission date Jun 12, 2012
Last update date Nov 28, 2012
Contact name Xianwen Zhang
E-mail(s) zhangxianwen@yahoo.com.cn
Organization name Hunan Agricultural University
Street address 1 Nongda Road, Furong District
City Changsha
State/province Hunan
ZIP/Postal code 410128
Country China
 
Platform ID GPL8852
Series (1)
GSE38665 Dynamic profile of gene expression in rice panicle under high temperature

Data table header descriptions
ID_REF
VALUE Log2 transformed Normalized signal intensity

Data table
ID_REF VALUE
Os01g0100100|COMBINER_EST|CI448596|0 -0.14598465
Os01g0100200|mRNA|AK059894|CDS+3'UTR -3.49E-04
Os01g0100400|mRNA|AK101455|CDS+3'UTR -0.23281384
Os01g0100500|mRNA|AK067316|CDS+3'UTR 0.10011196
Os01g0100600|mRNA|AK121362|CDS+3'UTR 0.08372879
Os01g0100700|mRNA|AK059844|CDS+3'UTR -0.20293045
Os01g0100700|mRNA|AK121523|CDS+3'UTR -0.1251421
Os01g0100800|mRNA|AK122012|CDS+3'UTR 0.14955711
Os01g0100900|COMBINER_EST|CI015509|0 0.5654688
Os01g0101200|mRNA|AK067866|CDS+3'UTR -0.06264973
Os01g0101200|mRNA|AK104517|CDS+3'UTR -0.061080933
Os01g0101200|mRNA|AK104625|CDS+3'UTR 0.084321976
Os01g0101200|mRNA|AK104752|CDS+3'UTR -0.004232407
Os01g0101200|mRNA|AK119457|CDS+3'UTR 0.07699537
Os01g0101300|COMBINER_EST|CI016681|6 -0.032850266
Os01g0101600|mRNA|AK099952|CDS+3'UTR 0.07565689
Os01g0101600|mRNA|AK103820|CDS+3'UTR -0.22907734
Os01g0101600|mRNA|AK122118|CDS+3'UTR -0.0905962
Os01g0101700|COMBINER_EST|CI525185|3 0.17672634
Os01g0101800|mRNA|AK103498|CDS+3'UTR -0.81722164

Total number of rows: 42475

Table truncated, full table size 1998 Kbytes.




Supplementary file Size Download File type/resource
GSM947264_US80803205_251524111336_S01_GE1-v5_95_Feb07_1_4.txt.gz 7.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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