2014
DOI: 10.1007/978-1-4939-0922-3_12
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Bimolecular Fluorescent Complementation (BiFC) by MAP Kinases and MAPK Phosphatases

Abstract: The adaptation of plants to the environment is a key property for survival. Adaptation responses to environmental cues are generated in cells by signaling initiated from cell receptors. Signal transduction is based on protein phosphorylation that is employed in mitogen-activated protein kinase (MAPK) cascades to integrate signals from receptors to cellular responses. MAPK activity is determined by phosphorylation of amino acid residues within the kinase activation loop and their dephosphorylation by phosphatas… Show more

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Cited by 6 publications
(4 citation statements)
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“…These observations are also consistent with a recent comprehensive analysis of the Arabidopsis proteome, which covers more than 14 000 proteins and where in ambient conditions the overall MKP1 abundance exceeds by far that of AP2C1 ( http://athena.proteomics.wzw.tum.de/ ) ( Mergner et al , 2020 ), underlining the rather specific role of AP2C1 under stress conditions. The AP2C1 paralogues AP2C2 and AP2C3 ( Umbrasaite et al , 2010 ; Umbrasaite et al , 2011 ; Schweighofer et al , 2014 ) as well as MKP1 and PTP1 interact with the same MAPKs and dephosphorylate them to various extents ( Bartels et al , 2009 ). However, the rather mild phenotypes of ap2c2 mkp1 and ap2c3 mkp1 plants, and the WT-like appearance of ap2c1 ptp1 ( Fig.…”
Section: Discussionmentioning
confidence: 99%
“…These observations are also consistent with a recent comprehensive analysis of the Arabidopsis proteome, which covers more than 14 000 proteins and where in ambient conditions the overall MKP1 abundance exceeds by far that of AP2C1 ( http://athena.proteomics.wzw.tum.de/ ) ( Mergner et al , 2020 ), underlining the rather specific role of AP2C1 under stress conditions. The AP2C1 paralogues AP2C2 and AP2C3 ( Umbrasaite et al , 2010 ; Umbrasaite et al , 2011 ; Schweighofer et al , 2014 ) as well as MKP1 and PTP1 interact with the same MAPKs and dephosphorylate them to various extents ( Bartels et al , 2009 ). However, the rather mild phenotypes of ap2c2 mkp1 and ap2c3 mkp1 plants, and the WT-like appearance of ap2c1 ptp1 ( Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Arabidopsis thaliana cell suspension cultures (ACSC) are an amenable, simplified model in which to study specific signaling mechanisms that would be too complex in plant tissues or organs. For instance, ACSC were recently used to study sugar signaling (Kunz et al, 2014), MAPK kinase and phosphatase signaling (Schweighofer et al, 2014), chitosan and galacturonide elicitor signaling (Ledoux et al, 2014), photooxidative damage (Gutiérrez et al, 2014), auxin transmembrane transport (Seifertová et al, 2014) and ion channel activity (Haapalainen et al, 2012). ACSC are easily labeled which is convenient for studying metabolic fluxes (Tjellström et al, 2012) like those in lipid phospholipid signaling.…”
Section: Introductionmentioning
confidence: 99%
“…These observations are also consistent with a recent comprehensive analysis of the Arabidopsis proteome, which covers more than 14,000 proteins and where in ambient conditions the overall MKP1 abundance outnumbers by far that of AP2C1 (http://athena.proteomics.wzw.tum.de/) (Mergner et al ., 2020), underlining the rather specific role of AP2C1 under stress conditions. The AP2C1 paralogues AP2C2 and AP2C3 (Schweighofer et al ., 2014; Umbrasaite et al ., 2010; Umbrasaite et al ., 2011) as well as MKP1 and PTP1 interact with the same MAPKs and dephosphorylate them to various extents (Bartels et al ., 2009). However, the rather mild phenotypes of ap2c2 mkp1 and ap2c3 mkp1 plants and the WT-like appearance of ap2c1 ptp1 (this work) compared to ap2c1 mkp1 plants clearly indicate specific genetic interactions and redundant functions of the evolutionary distant AP2C1 and MKP1 phosphatases in the regulation of signalling pathways.…”
Section: Discussionmentioning
confidence: 99%