Literature DB >> 30632760

MPK4 Phosphorylation Dynamics and Interacting Proteins in Plant Immunity.

Tong Zhang, Jacqueline D Schneider, Chuwei Lin, Sisi Geng, Tianyi Ma, Sheldon R Lawrence, Craig P Dufresne1, Alice C Harmon, Sixue Chen.   

Abstract

Arabidopsis MAP kinase 4 (MPK4) has been proposed to be a negative player in plant immunity, and it is also activated by pathogen-associated molecular patterns (PAMPs), such as flg22. The molecular mechanisms by which MPK4 is activated and regulates plant defense remain elusive. In this study, we investigated Arabidopsis defense against a bacterial pathogen Pseudomonas syringae pv tomato ( Pst) DC3000 when Brassica napus MPK4 ( BnMPK4) is overexpressed. We showed an increase in pathogen resistance and suppression of jasmonic acid (JA) signaling in the BnMPK4 overexpressing (OE) plants. We also showed that the OE plants have increased sensitivity to flg22-triggered reactive oxygen species (ROS) burst in guard cells, which resulted in enhanced stomatal closure compared to wild-type (WT). During flg22 activation, dynamic phosphorylation events within and outside of the conserved TEY activation loop were observed. To elucidate how BnMPK4 functions during the defense response, we used immunoprecipitation coupled with mass spectrometry (IP-MS) to identify BnMPK4 interacting proteins in the absence and presence of flg22. Quantitative proteomic analysis revealed a shift in the MPK4-associated protein network, providing insight into the molecular functions of MPK4 at the systems level.

Entities:  

Keywords:  IP−MS; MPK4; flg22; innate immunity; kinase substrate; protein−protein interaction

Mesh:

Substances:

Year:  2019        PMID: 30632760     DOI: 10.1021/acs.jproteome.8b00345

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  12 in total

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Authors:  Klaas J van Wijk; Tami Leppert; Qi Sun; Sascha S Boguraev; Zhi Sun; Luis Mendoza; Eric W Deutsch
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3.  Proteomic characterization of MPK4 signaling network and putative substrates.

Authors:  Tong Zhang; Shweta Chhajed; Jacqueline D Schneider; Guanqiao Feng; Wen-Yuan Song; Sixue Chen
Journal:  Plant Mol Biol       Date:  2019-08-09       Impact factor: 4.076

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Journal:  Int J Mol Sci       Date:  2020-11-28       Impact factor: 5.923

7.  PhosPhAt 4.0: An Updated Arabidopsis Database for Searching Phosphorylation Sites and Kinase-Target Interactions.

Authors:  Lin Xi; Zhaoxia Zhang; Waltraud X Schulze
Journal:  Methods Mol Biol       Date:  2021

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Authors:  Xuemei Zhang; Bowen Tan; Dan Zhu; Daniel Dufresne; Tingbo Jiang; Sixue Chen
Journal:  Int J Mol Sci       Date:  2021-06-15       Impact factor: 5.923

9.  The Arabidopsis Proteins AtNHR2A and AtNHR2B Are Multi-Functional Proteins Integrating Plant Immunity With Other Biological Processes.

Authors:  Raksha Singh; Rohana Liyanage; Chirag Gupta; Jackson O Lay; Andy Pereira; Clemencia M Rojas
Journal:  Front Plant Sci       Date:  2020-03-04       Impact factor: 5.753

10.  Facile One-Pot Nanoproteomics for Label-Free Proteome Profiling of 50-1000 Mammalian Cells.

Authors:  Kendall Martin; Tong Zhang; Tai-Tu Lin; Amber N Habowski; Rui Zhao; Chia-Feng Tsai; William B Chrisler; Ryan L Sontag; Daniel J Orton; Yong-Jie Lu; Karin D Rodland; Bin Yang; Tao Liu; Richard D Smith; Wei-Jun Qian; Marian L Waterman; H Steven Wiley; Tujin Shi
Journal:  J Proteome Res       Date:  2021-08-05       Impact factor: 4.466

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