1. Arabidopsis thaliana MAP65-1 and MAP65-2 function redundantly with MAP65-3/PLEIADE in cytokinesis downstream of MPK4.
- Author
-
Sasabe M, Kosetsu K, Hidaka M, Murase A, and Machida Y
- Subjects
- Arabidopsis genetics, Arabidopsis Proteins genetics, Flowers genetics, Gene Expression Regulation, Plant, Microtubule-Associated Proteins genetics, Mutation genetics, Phosphorylation, Plant Leaves genetics, Protein Transport, RNA, Messenger genetics, RNA, Messenger metabolism, Arabidopsis cytology, Arabidopsis enzymology, Arabidopsis Proteins metabolism, Cytokinesis, Microtubule-Associated Proteins metabolism
- Abstract
Plant cytokinesis occurs by the growth of cell plates from the interior to the periphery of the cell. These dynamic events in cytokinesis are mediated by a plant-specific microtubule (MT) array called the phragmoplast, which consists of bundled antiparallel MTs between the two daughter nuclei. The NACK-PQR pathway, a NACK1 kinesin-like protein and mitogen activated protein kinase (MAPK) cascade, is a key regulator of plant cytokinesis through the regulation of phragmoplast MTs. The MT-associated protein MAP65 has been identified as one of the structural components of MT assays involved in cell division, and we recently showed that Arabidopsis AtMAP65-3/PLEIADE (PLE) is a substrate of MPK4 that is a component of the NACK-PQR pathway in Arabidopsis. Here we show that AtMAP65-1 and AtMAP65-2 are also phosphorylated by MPK4. AtMAP65-1 and AtMAP65-2 that localize to the phragmoplast were phosphorylated by MPK4 in vitro. Although mutants of the Arabidopsis AtMAP65-1 and AtMAP65-2 genes exhibited a wild-type phenotype, double mutations of AtMAP65-3 and AtMAP65-1 or AtMAP65-2 caused more severe growth and cytokinetic defects than the single atmap65-3/ple mutation. These results suggest that AtMAP65-1 and AtMAP65-2 also function in cytokinesis downstream of MPK4.
- Published
- 2011
- Full Text
- View/download PDF