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有丝分裂原激活的蛋白激酶 4 参与拟南芥有丝分裂和胞质分裂过程中微管的转变调控。

Mitogen-activated protein kinase 4 is involved in the regulation of mitotic and cytokinetic microtubule transitions in Arabidopsis thaliana.

机构信息

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.

出版信息

New Phytol. 2011 Mar;189(4):1069-1083. doi: 10.1111/j.1469-8137.2010.03565.x. Epub 2010 Dec 14.

DOI:10.1111/j.1469-8137.2010.03565.x
PMID:21155826
Abstract

• 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.

摘要

• 一种丝裂原活化蛋白激酶激酶激酶(MAPKKK)双突变体,拟南芥核和质膜相关激酶(anp)同源物 anp2anp3,以及拟南芥的丝裂原活化蛋白激酶(MAPK)4 突变体 mpk4,表现出明显的胞质分裂缺陷。这促使我们分析了有丝分裂和胞质分裂的进展作为 MAPK 信号传导的功能。将突变体与未处理或用特定 MAPKK 抑制剂 PD98059 处理的野生型进行比较。• 本研究包括表型分析、MPK4 启动子的表达分析、MPK4、微管蛋白和 MAP65-1 的免疫荧光定位,以及对照、突变体和抑制剂处理细胞中有丝分裂微管(MT)转变的延时显微镜可视化。• 突变体和抑制剂处理的细胞表现出有丝分裂和胞质分裂缺陷,包括纺锤体和质膜形成异常以及有丝分裂和胞质分裂明显延迟或中止。结果,形成了双核和多核细胞,最终扰乱了营养组织的模式。MPK4 定位于扩展质膜的所有阶段,其模式与假定的底物 MAP65-1 相似。• 在本研究中,通过调节细胞分裂平面和胞质分裂进展,MPK4 被证明参与了有丝分裂/胞质分裂的调节。

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