The p38-like MAP kinase modulated H2O2 accumulation in wounding signaling pathways of sweet potato

Copyright © 2018 Elsevier B.V. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Plant science : an international journal of experimental plant biology. - 1985. - 280(2019) vom: 01. März, Seite 305-313
1. Verfasser: Lin, Hsin-Hung (VerfasserIn)
Weitere Verfasser: King, Yu-Chi, Li, Yu-Chi, Lin, Chih-Ching, Chen, Yu-Chi, Lin, Jeng-Shane, Jeng, Shih-Tong
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2019
Zugriff auf das übergeordnete Werk:Plant science : an international journal of experimental plant biology
Schlagworte:Journal Article Hydrogen peroxide Ipomoelin Sweet potato Wounding p38-like MAPK Enzyme Inhibitors Flavonoids Imidazoles Onium Compounds mehr... Plant Proteins Pyridines Okadaic Acid 1W21G5Q4N2 diphenyleneiodonium 6HJ411TU98 Hydrogen Peroxide BBX060AN9V p38 Mitogen-Activated Protein Kinases EC 2.7.11.24 SB 203580 OU13V1EYWQ 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one SJE1IO5E3I
Beschreibung
Zusammenfassung:Copyright © 2018 Elsevier B.V. All rights reserved.
In sweet potato (Ipomoea batatas cv Tainung 57), MAPK cascades are involved in the regulation of Ipomoelin (IPO) expression upon wounding. p38 MAPK plays an important role in plant's responses to various environmental stresses. However, the role of p38-like MAPK in wounding response is still unknown. In this study, the levels of phosphorylated-p38-like MAPK (pp38-like MAPK) in sweet potato were noticeably reduced after wounding. In addition, SB203580 (SB), a specific inhibitor blocking p38 MAPK phosphorylation, considerably decreased the accumulation of pp38-like MAPK. Expression of a wound-inducible gene IPO was elevated by SB. Moreover, it stimulated hydrogen peroxide (H2O2) production rather than cytosolic Ca2+ elevation in sweet potato leaves. However, NADPH oxidase (NOX) inhibitor diphenyleneiodonium could not inhibit IPO induction stimulated by SB. These results indicated a p38-like MAPK mechanism was involved in the regulation of IPO expression through NOX-independent H2O2 generation. In addition, the presence of the protein phosphatase inhibitor okadaic acid or the MEK1/ERK inhibitor PD98059 repressed the H2O2- or SB-induced IPO expression, demonstrating phosphatase(s) and MEK1/ERK functioning in the downstream of H2O2 and pp38-like MAPK in the signal transduction pathway stimulating IPO. Conclusively, wounding decreased the amount of pp38-like MAPK, stimulated H2O2 production, and then induced IPO expression
Beschreibung:Date Completed 18.03.2019
Date Revised 30.09.2020
published: Print-Electronic
Citation Status MEDLINE
ISSN:1873-2259
DOI:10.1016/j.plantsci.2018.12.011