Mitogen-activated protein kinase 4 is involved in the regulation of mitotic and cytokinetic microtubule transitions in Arabidopsis thaliana
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- aparát dělícího vřeténka účinky léků metabolismus MeSH
- Arabidopsis cytologie účinky léků enzymologie MeSH
- buněčné jádro účinky léků metabolismus MeSH
- cytokineze * účinky léků MeSH
- fenotyp MeSH
- flavonoidy farmakologie MeSH
- fluorescenční mikroskopie MeSH
- fluorescenční protilátková technika MeSH
- inhibitory proteinkinas farmakologie MeSH
- meristém cytologie účinky léků enzymologie MeSH
- mikrotubuly účinky léků metabolismus MeSH
- mitogenem aktivované proteinkinasy antagonisté a inhibitory metabolismus MeSH
- mitóza * účinky léků MeSH
- mutace genetika MeSH
- proteiny asociované s mikrotubuly metabolismus MeSH
- proteiny huseníčku antagonisté a inhibitory metabolismus MeSH
- viabilita buněk účinky léků MeSH
- zobrazování trojrozměrné MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one MeSH Prohlížeč
- AtMPK4 protein, Arabidopsis MeSH Prohlížeč
- flavonoidy MeSH
- inhibitory proteinkinas MeSH
- MAP65-1 protein, Arabidopsis MeSH Prohlížeč
- mitogenem aktivované proteinkinasy MeSH
- proteiny asociované s mikrotubuly MeSH
- proteiny huseníčku MeSH
• A mitogen-activated protein kinase kinase kinase (MAPKKK) double mutant, Arabidopsis homologue of nucleus and phragmoplast associated kinase (anp) anp2anp3, and the mitogen-activated protein kinase (MAPK) 4 mutant mpk4 of Arabidopsis thaliana show prominent cytokinetic defects. This prompted the analysis of mitotic and cytokinetic progression as a function of MAPK signalling. Mutants were compared with wild types untreated or treated with the specific MAPKK inhibitor PD98059. • This study included phenotype analysis, expression analysis of the MPK4 promoter, immunofluorescent localization of MPK4, tubulin and MAP65-1, and time-lapse microscopic visualization of the mitotic microtubule (MT) transitions in control, mutant and inhibitor-treated cells. • Mutant and inhibitor-treated cells showed defects in mitosis and cytokinesis, including aberrant spindle and phragmoplast formation and drastically delayed or abortive mitosis and cytokinesis. As a result, bi- and multinucleate cells were formed, ultimately disturbing the vegetative tissue patterning. MPK4 was localized to all stages of the expanding phragmoplast, in a pattern similar to that of its putative substrate MAP65-1. • In this study, MPK4 is shown to be involved in the regulation of mitosis/cytokinesis through modulation of the cell division plane and cytokinetic progression.
Institut für Zelluläre und Molekulare Botanik Universität Bonn Kirschallee 1 D53115 Bonn Germany
Institute of General Botany Faculty of Biology University of Athens GR15784 Greece
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