NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE75377 Query DataSets for GSE75377
Status Public on Nov 24, 2018
Title Antagonistic Regulation of Abscisic Acid Inhibited Root Growth By Brassinosteroid is Partially Mediated by BRASSINAZOLE RESISTENT 1 suppressed ABSCISIC ACID INSENSITIVE 5 expression
Organism Arabidopsis thaliana
Experiment type Expression profiling by high throughput sequencing
Summary Plant hormone brassinosteroids (BRs) and abscisic acids (ABA) antagonistically regulate many aspects of plant growth and responses. This study analyzes the molecular mechanisms by which regulate the crosstalk between BR and ABA signaling.Various BR deficient and gain-of-function signaling mutants were used to analyze their responses to ABA inhibited primary root growth. RNA sequencing was performed to identify the ABA regulated root genes that are also regulated by BR signaling components.Our result demonstrated that BR signaling negative regulates plant ABA response, and the crosstalk is mediated by BIN2 and BZR1. RNA sequencing has identified subsets of ABA responsive root genes that were regulated by BIN2 and/or BZR1. ChIP-qPCR and EMSA assays showed that BZR1 could bind directly with several G-box cis-elements on ABI5 promoter, suppress the expression of ABI5 and makes plant insensitive to ABA.These data demonstrated that ABI5 is a BZR1 direct targeted gene. Regulation of ABI5 expression by BZR1 plays important roles in regulating the crosstalk between BR and ABA signaling pathways.
 
Overall design Arabidopsis Col, bin2-1 and bzr1-D/bin2-1 were grown vertically on 1/2 MS in chamber for 7 days and then treated with or without 100 μM ABA for 3 h . The roots about 1 cm from the tips were excised and collected for RNA extraction. Total RNA was extracted using a RNeasy Plant Mini Kit (Qiagen) and the concentration was quantified on Nanodrop 1000 (Thermo). The mRNA sequencing libraries were constructed with barcodes using the TruSeq RNA Sample Preparation Kit (Illumina). Six barcoded libraries were pooled together and sequenced by Illumina HiSeq2000.
 
Contributor(s) Yang X, Tang W
Citation(s) 27149247
Submission date Nov 24, 2015
Last update date May 17, 2021
Contact name Wenqiang Tang
E-mail(s) tangwq2015@163.com
Organization name Hebei Normal University
Department College of Life Sciences
Street address East 20 NanErHuang Road
City Shijiazhuang
State/province Hebei Province
ZIP/Postal code 050024
Country China
 
Platforms (1)
GPL13222 Illumina HiSeq 2000 (Arabidopsis thaliana)
Samples (8)
GSM1954212 Col-ABA
GSM1954213 Col+ABA
GSM1954214 bin2-1
Relations
BioProject PRJNA304022
SRA SRP066634

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
GSE75377_Col+ABA_vs_Col-ABA_original_data.xls.gz 1.8 Mb (ftp)(http) XLS
GSE75377_bin2-1_vs_Col-ABA_original_data.xls.gz 1.8 Mb (ftp)(http) XLS
GSE75377_bzr1-Dbin2-1_vs_bin2-1_original_data.xls.gz 1.8 Mb (ftp)(http) XLS
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap