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细胞板相关 PI4Kβ 在植物体细胞胞质分裂过程中对胞吞作用和胞质环动态的双重作用。

A dual role for cell plate-associated PI4Kβ in endocytosis and phragmoplast dynamics during plant somatic cytokinesis.

机构信息

Department of Cellular Biochemistry, Institute of Biochemistry and Biotechnology, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.

Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Seeland, Germany.

出版信息

EMBO J. 2019 Feb 15;38(4). doi: 10.15252/embj.2018100303. Epub 2019 Jan 7.

Abstract

Plant cytokinesis involves membrane trafficking and cytoskeletal rearrangements. Here, we report that the phosphoinositide kinases PI4Kβ1 and PI4Kβ2 integrate these processes in () roots. Cytokinetic defects of an double mutant are accompanied by defects in membrane trafficking. Specifically, we show that trafficking of the proteins KNOLLE and PIN2 at the cell plate, clathrin recruitment, and endocytosis is impaired in double mutants, accompanied by unfused vesicles at the nascent cell plate and around cell wall stubs. Interestingly, plants also display ectopic overstabilization of phragmoplast microtubules, which guide membrane trafficking at the cell plate. The overstabilization of phragmoplasts in the double mutant coincides with mislocalization of the microtubule-associated protein 65-3 (MAP65-3), which cross-links microtubules and is a downstream target for inhibition by the MAP kinase MPK4. Based on similar cytokinetic defects of the and mutants and genetic and physical interaction of PI4Kβ1 and MPK4, we propose that PI4Kβ and MPK4 influence localization and activity of MAP65-3, respectively, acting synergistically to control phragmoplast dynamics.

摘要

植物胞质分裂涉及膜运输和细胞骨架重排。在这里,我们报告说,磷酸肌醇激酶 PI4Kβ1 和 PI4Kβ2 在 () 根中整合了这些过程。双突变体的胞质分裂缺陷伴随着膜运输缺陷。具体而言,我们表明,KNOLLE 和 PIN2 蛋白在细胞板处的运输、网格蛋白募集和内吞作用受损,在 双突变体中,未融合的小泡在新形成的细胞板和细胞壁残余物周围。有趣的是, 植物还表现出初生细胞板处膜运输的桥粒微管的异位过度稳定。双突变体中桥粒的过度稳定与微管相关蛋白 65-3(MAP65-3)的定位错误同时发生,MAP65-3 交联微管,是 MAP 激酶 MPK4 抑制的下游靶标。基于 和 突变体类似的胞质分裂缺陷以及 PI4Kβ1 和 MPK4 的遗传和物理相互作用,我们提出 PI4Kβ 和 MPK4 分别影响 MAP65-3 的定位和活性,协同作用以控制桥粒动力学。

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