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Quantitative phosphoproteomic analysis reveals common regulatory mechanisms of immune components during effector- and PAMP-triggered immunity

ABSTRACT: The dataset for this project was to identify significantly regulated phosphorylation sites of membrane-associated proteins during RPS2-mediated effector-triggered immunity in Arabidopsis.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Arabidopsis Thaliana (mouse-ear Cress)

TISSUE(S): Plant Cell, Leaf

SUBMITTER: Thomas Liebrand

LAB HEAD: Gitta Coaker

PROVIDER: PXD010440 | Pride | 2018-10-11

REPOSITORIES: Pride

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			Action	DRS
	Raw_File_explanation.docx	Other
	andromeda_phosphoenriched.zip	Other
	andromeda_unenriched.zip	Other
	modificationSpecificPeptides_phosphoenriched.txt	Txt
	modificationSpecificPeptides_unenriched.txt	Txt

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Publications

Quantitative phosphoproteomic analysis reveals common regulatory mechanisms between effector- and PAMP-triggered immunity in plants.

Kadota Yasuhiro Y Liebrand Thomas W H TWH Goto Yukihisa Y Sklenar Jan J Derbyshire Paul P Menke Frank L H FLH Torres Miguel-Angel MA Molina Antonio A Zipfel Cyril C Coaker Gitta G Shirasu Ken K

The New phytologist 20181105 4

Plant immunity consists of two arms: pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI), induced by surface-localized receptors, and effector-triggered immunity (ETI), induced by intracellular receptors. Despite the little structural similarity, both receptor types activate similar responses with different dynamics. To better understand phosphorylation events during ETI, we employed a phosphoproteomic screen using an inducible expression system of the bacterial effector avrRpt ...[more]

PMID: 30300945

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