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Involvement of YODA and mitogen activated protein kinase 6 in Arabidopsis post-embryogenic root development through auxin up-regulation and cell division plane orientation
V. Smékalová, I. Luptovčiak, G. Komis, O. Šamajová, M. Ovečka, A. Doskočilová, T. Takáč, P. Vadovič, O. Novák, T. Pechan, A. Ziemann, P. Košútová, J. Šamaj,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1902 to 1 year ago
Wiley Free Content
from 1997 to 1 year ago
PubMed
24923680
DOI
10.1111/nph.12880
Knihovny.cz E-resources
- MeSH
- Arabidopsis cytology drug effects embryology enzymology MeSH
- Cell Division * drug effects MeSH
- Cytokinesis drug effects MeSH
- Plant Epidermis cytology MeSH
- Phenotype MeSH
- Fluorescent Antibody Technique MeSH
- Phosphorylation drug effects MeSH
- Interphase MeSH
- Plant Roots anatomy & histology cytology embryology MeSH
- Indoleacetic Acids metabolism pharmacology MeSH
- MAP Kinase Kinase Kinases metabolism MeSH
- Meristem cytology drug effects MeSH
- Microtubules drug effects metabolism MeSH
- Mitogen-Activated Protein Kinases metabolism MeSH
- Mitosis drug effects MeSH
- Mutation genetics MeSH
- Arabidopsis Proteins metabolism MeSH
- Proteomics MeSH
- Protein Transport drug effects MeSH
- Up-Regulation * drug effects MeSH
- Protein Binding drug effects MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The role of YODA MITOGEN ACTIVATED PROTEIN KINASE KINASE KINASE 4 (MAPKKK4) upstream of MITOGEN ACTIVATED PROTEIN KINASE 6 (MPK6) was studied during post-embryonic root development of Arabidopsis thaliana. Loss- and gain-of-function mutants of YODA (yda1 and ΔNyda1) were characterized in terms of root patterning, endogenous auxin content and global proteomes. We surveyed morphological and cellular phenotypes of yda1 and ΔNyda1 mutants suggesting possible involvement of auxin. Endogenous indole-3-acetic acid (IAA) levels were up-regulated in both mutants. Proteomic analysis revealed up-regulation of auxin biosynthetic enzymes tryptophan synthase and nitrilases in these mutants. The expression, abundance and phosphorylation of MPK3, MPK6 and MICROTUBULE ASSOCIATED PROTEIN 65-1 (MAP65-1) were characterized by quantitative polymerase chain reaction (PCR) and western blot analyses and interactions between MAP65-1, microtubules and MPK6 were resolved by quantitative co-localization studies and co-immunoprecipitations. yda1 and ΔNyda1 mutants showed disoriented cell divisions in primary and lateral roots, abortive cytokinesis, and differential subcellular localization of MPK6 and MAP65-1. They also showed deregulated expression of TANGLED1 (TAN1), PHRAGMOPLAST ORIENTING KINESIN 1 (POK1), and GAMMA TUBULIN COMPLEX PROTEIN 4 (GCP4). The findings that MPK6 localized to preprophase bands (PPBs) and phragmoplasts while the mpk6-4 mutant transformed with MPK6AEF (alanine (A)-glutamic acid (E)-phenylanine (F)) showed a root phenotype similar to that of yda1 demonstrated that MPK6 is an important player downstream of YODA. These data indicate that YODA and MPK6 are involved in post-embryonic root development through an auxin-dependent mechanism regulating cell division and mitotic microtubule (PPB and phragmoplast) organization.
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