Protein phosphatase AP2C1 negatively regulates basal resistance and defense responses to Pseudomonas syringae

© The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology.

Bibliographische Detailangaben
Veröffentlicht in:Journal of experimental botany. - 1985. - 68(2017), 5 vom: 01. Feb., Seite 1169-1183
1. Verfasser: Shubchynskyy, Volodymyr (VerfasserIn)
Weitere Verfasser: Boniecka, Justyna, Schweighofer, Alois, Simulis, Justinas, Kvederaviciute, Kotryna, Stumpe, Michael, Mauch, Felix, Balazadeh, Salma, Mueller-Roeber, Bernd, Boutrot, Freddy, Zipfel, Cyril, Meskiene, Irute
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2017
Zugriff auf das übergeordnete Werk:Journal of experimental botany
Schlagworte:Journal Article Callose MAPK MAPK phosphatase PAMP PP2C phosphatase Pseudomonas syringae defense genes salicylic acid transcription factors. mehr... Arabidopsis Proteins Mitogen-Activated Protein Kinases EC 2.7.11.24 AP2C1 protein, Arabidopsis EC 3.1.3.16 Phosphoprotein Phosphatases MKP1 protein, Arabidopsis EC 3.1.3.48 Protein Tyrosine Phosphatases
Beschreibung
Zusammenfassung:© The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology.
Mitogen-activated protein kinases (MAPKs) mediate plant immune responses to pathogenic bacteria. However, less is known about the cell autonomous negative regulatory mechanism controlling basal plant immunity. We report the biological role of Arabidopsis thaliana MAPK phosphatase AP2C1 as a negative regulator of plant basal resistance and defense responses to Pseudomonas syringae. AP2C2, a closely related MAPK phosphatase, also negatively controls plant resistance. Loss of AP2C1 leads to enhanced pathogen-induced MAPK activities, increased callose deposition in response to pathogen-associated molecular patterns or to P. syringae pv. tomato (Pto) DC3000, and enhanced resistance to bacterial infection with Pto. We also reveal the impact of AP2C1 on the global transcriptional reprogramming of transcription factors during Pto infection. Importantly, ap2c1 plants show salicylic acid-independent transcriptional reprogramming of several defense genes and enhanced ethylene production in response to Pto. This study pinpoints the specificity of MAPK regulation by the different MAPK phosphatases AP2C1 and MKP1, which control the same MAPK substrates, nevertheless leading to different downstream events. We suggest that precise and specific control of defined MAPKs by MAPK phosphatases during plant challenge with pathogenic bacteria can strongly influence plant resistance
Beschreibung:Date Completed 16.11.2017
Date Revised 29.01.2022
published: Print
Citation Status MEDLINE
ISSN:1460-2431
DOI:10.1093/jxb/erw485