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Series GSE80422 Query DataSets for GSE80422
Status Public on Dec 11, 2017
Title Time course RNA-seq analysis of expression changes upon MLACC expression in Arabidopsis using a dexamethasone-inducible system which mirrors NLR activation
Organism Arabidopsis thaliana
Experiment type Expression profiling by high throughput sequencing
Summary Innate immune responses of plant cells confer the first line of defence against pathogens. Signals generated by activated receptors are integrated inside the cell and converge on transcriptional programmes in the nucleus. The barley NLR intracellular receptor MLA is fully functionnal in Arabidopsis and the MLA N-terminal coiled-coil domain (MLACC) is sufficient for initiating the MLA-dependent immune signalling. Using RNA-seq, we analyzed the early MLACC-mediated transcriptional changes over time in a dexamethasone-inducible and pathogen-independent system.
 
Overall design We used transgenic Arabidopsis plants expressing MLACC-mYFP under a dexamethasone-inducible promoter (DEXp), a genetic background in which an immune-like response can be turned on rapidly and synchronously in leaf cells after dexamethasone treatment. We used transgenic lines in WT and in the phytohormone-depleted and partially immunocompromised pen2 pad4 sag101 dde2 ein2 sid2 (ppsdes) sextuple mutant backgrounds to assess the contribution of the three main defense phytohormones (jasmonate, ethylene, salycilic acid) in the MLACC-mediated immune signalling. In order to substract defense-unrelated artifacts due to the dexamethasone treatment, we used plants expressing the mYFP under the dexamethasone-inducible promoter in WT background and non-transgenic sextuple mutant plants in parallel as negative control. Samples were collected at 0, 2, 4, 6, and 8 hours after dexamethasone infiltration into leaves. For each condition, three biological replicates were obtained.
 
Contributor(s) Jacob F, Kracher B, Maekawa T, Schulze-Lefert P
Citation(s) 29226970
Submission date Apr 19, 2016
Last update date May 15, 2019
Contact name Barbara Kracher
E-mail(s) [email protected]
Organization name Max Planck Institute for Plant Breeding Research
Department Plant-Microbe Interactions
Street address Carl-von-Linné-Weg 10
City Cologne
ZIP/Postal code 50829
Country Germany
 
Platforms (1)
GPL17639 Illumina HiSeq 2500 (Arabidopsis thaliana)
Samples (60)
GSM2127005 DEXp:mYFP plants infiltrated with dexamethasone, 0 h, rep1
GSM2127006 DEXp:mYFP plants infiltrated with dexamethasone, 0 h, rep2
GSM2127007 DEXp:mYFP plants infiltrated with dexamethasone, 0 h, rep3
Relations
BioProject PRJNA318880
SRA SRP073485

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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE80422_CountTable_At_1493_raw.txt.gz 1.1 Mb (ftp)(http) TXT
GSE80422_CountTable_At_1725_raw.txt.gz 1.1 Mb (ftp)(http) TXT
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