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Series GSE6832 Query DataSets for GSE6832
Status Public on Jan 22, 2007
Title Cytokinin treatment on aerial parts of seedlings
Organism Arabidopsis thaliana
Experiment type Expression profiling by array
Summary In Arabidopsis thaliana, the immediate early response of plants to cytokinin is formulated as the multistep AHK-AHP-ARR phosphorelay signaling circuitry, which is initiated by the cytokinin-receptor histidine protein kinases. In the hope of finding components (or genes) that function downstream of the cytokinin-mediated His-Asp phosphorelay signaling circuitry, we carried out genome-wide microarray analyses. To this end, we focused on a pair of highly homologous ARR10 and ARR12 genes by constructing an arr10 arr12 double null mutant. The mutant alleles used in this study were arr10-5 and arr12-1. arr10-5 is the SALK_098604 T-DNA insertion line, whose mutation was determined to be located in the fifth exon of the ARR10 coding sequence. Arr12-1 is the SALK_054752 T-DNA insertion line, whose mutation was determined to be located in the third exon of the ARR12 coding sequence. The resulting mutant exhibits a characteristic phenotype with regard to the cytokinin-mediated His-Asp phosphorelay. Here we, therefore, compared response to cytokinin in wild type with that in arr10 arr12 double mutant. In this study, wild type and the arr10 arr12 double mutant grown vertically on MS agar plates for 2 weeks were treated with 20uM t-zeatin or 0.02% DMSO (solvent for t-zetion solution) for 1h. These treated plant samples were divided into three portions, from which RNA samples were prepared separately from aerial parts of seedlings with use of RNeasy Plant Mini Kit (Qiagen, Valencia, CA, U.S.A.). The Quality of RNAs prepared was analyzed by Bioanalyzer 2100 (Agilent Technologies). These RNA samples were processed as recommended by the Affymetrix instruction (Affymetrix GeneChip Expression Analysis Technical Manual, Affymetrix). These dataset will provide us with bases for understanding the early response to cytokinin on aerial parts of seedlings in Arabidopsis thaliana.
Experimenter name: Hitoshi SAKAKIBARA
Experimenter phone: 81455039576
Experimenter fax: 81455039609
Experimenter address: Biodynamics Research Team
Experimenter address: RIKEN Plant Science Center
Experimenter address: 1-7-22 Suehiro, Tsurumi
Experimenter address: Yokohama
Experimenter zip/postal_code: 230-0045
Experimenter country: JAPAN
Keywords: compound_treatment_design;
 
Overall design 12 samples were used in this experiment
 
Contributor(s) SAKAKIBARA H, Townsend H, Emmerson Z, Schildknecht B
Citation(s) 17132632
Submission date Jan 22, 2007
Last update date Aug 28, 2018
Contact name Nottingham Arabidopsis Stock Centre (NASC)
E-mail(s) [email protected]
Phone +44 (0)115 951 3237
Fax +44 (0)115 951 3297
URL http://arabidopsis.info/
Organization name Nottingham Arabidopsis Stock Centre (NASC)
Department School of Biosciences, University of Nottingham
Street address Sutton Bonington Campus
City Loughborough
ZIP/Postal code LE12 5RD
Country United Kingdom
 
Platforms (1)
GPL198 [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array
Samples (12)
GSM157382 Sakakibara_1-1_TZ-treatment-wild_Rep1_ATH1
GSM157383 Sakakibara_1-2_TZ-treatment-wild_Rep2_ATH1
GSM157384 Sakakibara_1-3_TZ-treatment-wild_Rep3_ATH1
Relations
Affiliated with GSE69995
BioProject PRJNA99159

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE6832_RAW.tar 26.3 Mb (http)(custom) TAR (of CEL)

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