|
| Status |
Public on Jun 01, 2015 |
| Title |
Dexamethasone inducible amiAP3 2 |
| Sample type |
RNA |
| |
|
| Channel 1 |
| Source name |
whole infloresence
|
| Organism |
Arabidopsis thaliana |
| Characteristics |
treatment: Mock
genotype: FIS (ap1 cal1 AP1-GR) LhG4-GR:amiAP3
|
| Treatment protocol |
For all experiments, ~4 week-old plants were used. For experiments using the FIS (35S:AP1-GR ap1-1 cal-1 plants), flower development was induced using a solution containing 10 μM dexamethasone (Sigma-Aldrich), 0.01% (v/v) ethanol and 0.015% (v/v) Silwet L-77 (De Sangosse) – as described in Wellmer F, et al. (2006) Genome-Wide Analysis of Gene Expression during Early Arabidopsis Flower Development. PLoS Genetics 2(7):e117.
|
| Growth protocol |
Plants were grown on a soil:vermiculite:perlite (3:1:1) mixture at 20 degrees (16 degrees for plants used for temperature-sensitive perturbation experiments) under constant illumination with cool white fluorescent light
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Total RNA was isolated from tissue samples using the Plant Total RNA kit (Sigma-Aldrich), according to the manufacturer's instructions
|
| Label |
Cy3
|
| Label protocol |
500ng of total RNA were primed with 0.6µl of T7 DNA primer at 65°C for 10 min, then reverse transcribed at 40°C for 2 hrs in the presence of 300 U MMLV Reverse Transcriptase and 10mM dNTP mix, with Cy3-label and Cy5- label.
|
| |
|
| Channel 2 |
| Source name |
whole infloresence
|
| Organism |
Arabidopsis thaliana |
| Characteristics |
treatment: Dexamethazone
genotype: FIS (ap1 cal1 AP1-GR) LhG4-GR:amiAP3
|
| Treatment protocol |
For all experiments, ~4 week-old plants were used. For experiments using the FIS (35S:AP1-GR ap1-1 cal-1 plants), flower development was induced using a solution containing 10 μM dexamethasone (Sigma-Aldrich), 0.01% (v/v) ethanol and 0.015% (v/v) Silwet L-77 (De Sangosse) – as described in Wellmer F, et al. (2006) Genome-Wide Analysis of Gene Expression during Early Arabidopsis Flower Development. PLoS Genetics 2(7):e117.
|
| Growth protocol |
Plants were grown on a soil:vermiculite:perlite (3:1:1) mixture at 20 degrees (16 degrees for plants used for temperature-sensitive perturbation experiments) under constant illumination with cool white fluorescent light
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Total RNA was isolated from tissue samples using the Plant Total RNA kit (Sigma-Aldrich), according to the manufacturer's instructions
|
| Label |
Cy5
|
| Label protocol |
500ng of total RNA were primed with 0.6µl of T7 DNA primer at 65°C for 10 min, then reverse transcribed at 40°C for 2 hrs in the presence of 300 U MMLV Reverse Transcriptase and 10mM dNTP mix, with Cy3-label and Cy5- label.
|
| |
|
| |
| Hybridization protocol |
Fragmentation buffer and Hybridization Buffer HI-RPM (Agilent Gene Expression Hybridization Kit) were added and samples were applied to microarrays enclosed in Agilent SureHyb-enabled hybridization chambers and hybridized for 16 hrs at 65°C. After hybridization, slides were washed sequentially according to the manufacturer's instruction.
|
| Scan protocol |
Scanned on an Agilent G2565AA scanner. Images were quantified using Agilent Feature Extraction Software (v 10.5.1).
|
| Description |
Biological replicate 2
|
| Data processing |
Agilent Feature Extraction Software (v 10.5.1) was used for background subtraction and LOWESS normalization
|
| |
|
| Submission date |
Apr 22, 2015 |
| Last update date |
Jun 01, 2015 |
| Contact name |
Pat Ryan |
| E-mail(s) |
[email protected]
|
| Organization name |
TCD
|
| Street address |
College Green
|
| City |
Dublin |
| ZIP/Postal code |
na |
| Country |
Ireland |
| |
|
| Platform ID |
GPL20094 |
| Series (1) |
| GSE68157 |
Gene network analysis in Arabidopsis thaliana flower development through dynamic gene perturbations |
|
