The Arabidopsis mitogen-activated protein kinase 6 is associated with γ-tubulin on microtubules, phosphorylates EB1c and maintains spindle orientation under nitrosative stress
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
BB/F00964X/1
Biotechnology and Biological Sciences Research Council - United Kingdom
BBS/B/13314
Biotechnology and Biological Sciences Research Council - United Kingdom
PubMed
26061286
DOI
10.1111/nph.13501
Knihovny.cz E-resources
- Keywords
- Arabidopsis, EB1c, MPK6, cell division, microtubules, mitogen-activated protein kinase, nitrosative stress, γ-tubulin,
- MeSH
- Anaphase drug effects MeSH
- Spindle Apparatus drug effects metabolism MeSH
- Arabidopsis cytology drug effects enzymology MeSH
- Butadienes pharmacology MeSH
- Cytokinesis drug effects MeSH
- Extracellular Signal-Regulated MAP Kinases metabolism MeSH
- Phosphorylation drug effects MeSH
- Stress, Physiological * drug effects MeSH
- Kinetochores drug effects metabolism MeSH
- Meristem cytology drug effects metabolism MeSH
- Microtubules drug effects metabolism MeSH
- Mitogen-Activated Protein Kinases metabolism MeSH
- Nitriles pharmacology MeSH
- Nitrosation drug effects MeSH
- Cell Proliferation drug effects MeSH
- Microtubule-Associated Proteins metabolism MeSH
- Arabidopsis Proteins metabolism MeSH
- Plant Cells drug effects metabolism MeSH
- Chromosome Segregation drug effects MeSH
- Telophase drug effects MeSH
- Tubulin metabolism MeSH
- Tyrosine analogs & derivatives pharmacology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 3-nitrotyrosine MeSH Browser
- Butadienes MeSH
- EB1c protein, Arabidopsis MeSH Browser
- Extracellular Signal-Regulated MAP Kinases MeSH
- Mitogen-Activated Protein Kinases MeSH
- MPK6 protein, Arabidopsis MeSH Browser
- Nitriles MeSH
- Microtubule-Associated Proteins MeSH
- Arabidopsis Proteins MeSH
- Tubulin MeSH
- Tyrosine MeSH
- U 0126 MeSH Browser
Stress-activated plant mitogen-activated protein (MAP) kinase pathways play roles in growth adaptation to the environment by modulating cell division through cytoskeletal regulation, but the mechanisms are poorly understood. We performed protein interaction and phosphorylation experiments with cytoskeletal proteins, mass spectrometric identification of MPK6 complexes and immunofluorescence analyses of the microtubular cytoskeleton of mitotic cells using wild-type, mpk6-2 mutant and plants overexpressing the MAP kinase-inactivating phosphatase, AP2C3. We showed that MPK6 interacted with γ-tubulin and co-sedimented with plant microtubules polymerized in vitro. It was the active form of MAP kinase that was enriched with microtubules and followed similar dynamics to γ-tubulin, moving from poles to midzone during the anaphase-to-telophase transition. We found a novel substrate for MPK6, the microtubule plus end protein, EB1c. The mpk6-2 mutant was sensitive to 3-nitro-l-tyrosine (NO2 -Tyr) treatment with respect to mitotic abnormalities, and root cells overexpressing AP2C3 showed defects in chromosome segregation and spindle orientation. Our data suggest that the active form of MAP kinase interacts with γ-tubulin on specific subsets of mitotic microtubules during late mitosis. MPK6 phosphorylates EB1c, but not EB1a, and has a role in maintaining regular planes of cell division under stress conditions.
Institute of Biotechnology University of Vilnius Vilnius Lithuania
Institute of Microbiology AS CR v v i Vídeňská 1083 142 20 Prague 4 Czech Republic
Max F Perutz Laboratories University of Vienna Vienna Austria
School of Biological Sciences Royal Holloway University of London Egham Surrey TW20 0EX UK
Technical Analytical Research Group of HAS Szent Gellért tér 4 H 1111 Budapest Hungary
References provided by Crossref.org
Microtubular and Nuclear Functions of γ-Tubulin: Are They LINCed?
Phosphorylation of Plant Microtubule-Associated Proteins During Cell Division