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植物胞质分裂和成膜体结构的分子解析:对绿色荧光蛋白标记蛋白的综述

Molecular dissection of plant cytokinesis and phragmoplast structure: a survey of GFP-tagged proteins.

作者信息

Van Damme Daniël, Bouget François-Yves, Van Poucke Kris, Inzé Dirk, Geelen Danny

机构信息

Department of Plant Systems Biology, Flanders Interuniversity Institute for Biotechnology, Ghent University, Technologiepark 927, B-9052 Gent, Belgium.

出版信息

Plant J. 2004 Nov;40(3):386-98. doi: 10.1111/j.1365-313X.2004.02222.x.

Abstract

To identify molecular players implicated in cytokinesis and division plane determination, the Arabidopsis thaliana genome was explored for potential cytokinesis genes. More than 100 open reading frames were selected based on similarity to yeast and animal cytokinesis genes, cytoskeleton and polarity genes, and Nicotiana tabacum genes showing cell cycle-controlled expression. The subcellular localization of these proteins was determined by means of GFP tagging in tobacco Bright Yellow-2 cells and Arabidopsis plants. Detailed confocal microscopy identified 15 proteins targeted to distinct regions of the phragmoplast and the cell plate. EB1- and MAP65-like proteins were associated with the plus-end, the minus-end, or along the entire length of microtubules. The actin-binding protein myosin, the kinase Aurora, and a novel cell cycle protein designated T22, accumulated preferentially at the midline. EB1 and Aurora, in addition to other regulatory proteins (homologs of Mob1, Sid1, and Sid2), were targeted to the nucleus, suggesting that this organelle operates as a coordinating hub for cytokinesis.

摘要

为了鉴定参与胞质分裂和分裂平面确定的分子因子,对拟南芥基因组进行了探索,以寻找潜在的胞质分裂基因。基于与酵母和动物胞质分裂基因、细胞骨架和极性基因以及显示细胞周期控制表达的烟草基因的相似性,选择了100多个开放阅读框。通过在烟草Bright Yellow-2细胞和拟南芥植物中进行绿色荧光蛋白(GFP)标记,确定了这些蛋白质的亚细胞定位。详细的共聚焦显微镜观察鉴定出15种蛋白质定位于成膜体和细胞板的不同区域。EB1和类MAP65蛋白与微管的正端、负端或整个长度相关。肌动蛋白结合蛋白肌球蛋白、激酶极光激酶和一种名为T22的新型细胞周期蛋白优先聚集在中线处。EB1和极光激酶,以及其他调节蛋白(Mob1、Sid1和Sid2的同源物)定位于细胞核,这表明该细胞器作为胞质分裂的协调中心发挥作用。

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