E-GEOD-25134 - Transcription profiling by array of Arabidopsis mutant for bzr1 and bri1 or bri1 only

Released on 31 December 2010, last updated on 30 April 2015
Arabidopsis thaliana
Samples (9)
Array (1)
Protocols (8)
Molecular genetic analyses support a central role of BZR1 in Brassinosteroid (BR) regulation of plant development. The dominant bzr1-1D mutation, which stabilizes the BZR1 protein, completely suppresses the de-etiolated phenotype of the null bri1-116 mutant grown in the dark. Using microarray analysis, we identified genes differentially expressed in bri1-116 compared to wild type and genes differentially expressed in the bzr1-1D;bri1-116 double mutant compared to the bri1-116 single mutant. Consistent with the phenotypic suppression of bri1-116 by bzr1-1D, about 80% of the genes affected in bri1-116 were affected oppositely by bzr1-1D BZR1 regulated genes were generated from comparing genes differentially expressed by bzr1-1D;bri1-116 and bri1-116. Genes affected by BRI1 were generated from comparing differentially expressed genes of bri1-116 and Col control. ANOVA was used to find genes whose expression was different between bzr1-1D;bri1-116 and bri1-116 or between bri1-116 and Col samples [see Supplementary file below].
Experiment types
transcription profiling by array, genetic modification design
Integration of brassinosteroid signal transduction with the transcription network for plant growth regulation in Arabidopsis. Sun Y, Fan XY, Cao DM, Tang W, He K, Zhu JY, He JX, Bai MY, Zhu S, Oh E, Patil S, Kim TW, Ji H, Wong WH, Rhee SY, Wang ZY.
Investigation descriptionE-GEOD-25134.idf.txt
Sample and data relationshipE-GEOD-25134.sdrf.txt
Raw data (1)E-GEOD-25134.raw.1.zip
Processed data (1)E-GEOD-25134.processed.1.zip
Array designA-AFFY-2.adf.txt