Where are the limits of the centrosome?

Irina B Alieva, Rustem E Uzbekov
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引用次数: 8

Abstract

The centrosome is a key component of the cell is involved in the processes of cell division, cell motility, intracellular transport, organization of the microtubules (MT) network and the production of cilia and flagella. The peculiarity of this organelle is that its boundaries are not clearly defined, the centrioles at the center of the centrosome are surrounded by electron dense pericentriolar material, the size and protein composition of this centrosome component experiences significant transformation during the cell cycle. It has been shown in this study that within the centrosome different proteins occupy different areas corresponding to: MT nucleation region (defined as gamma-tubulin-stained area), regulatory region (defined as kinase pEg2-stained area) and motor proteins region (kinesin-like motor XlEg5-stained area). The boundary of pEg2 is near 1.3 times greater while XlEg5 is 3.0 times greater than that of gamma-tubulin. Thus, the size of the centrosome, determined according to the structural electron microscopy (EM) analysis (about 1 µm) corresponds to the regulatory proteins area, but the actual functional centrosome size defined at the motor proteins region, is more than twice the size.

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中心体的界限在哪里?
中心体是细胞的关键组成部分,参与细胞分裂、细胞运动、细胞内运输、微管网络的组织以及纤毛和鞭毛的产生。该细胞器的特点是其边界不明确,中心体中心的中心粒被电子密集的中心粒周围物质包围,该中心体成分的大小和蛋白质组成在细胞周期中发生了显著的变化。本研究表明,在中心体内,不同的蛋白占据不同的区域,对应于:MT成核区(定义为γ -微管蛋白染色区域),调控区(定义为激酶peg2染色区域)和运动蛋白区(运动蛋白样运动xleg5染色区域)。pEg2的边界比γ -微管蛋白大1.3倍,XlEg5的边界比γ -微管蛋白大3.0倍。因此,根据结构电子显微镜(EM)分析确定的中心体大小(约1µm)对应于调节蛋白区域,但在运动蛋白区域定义的实际功能中心体大小是其大小的两倍以上。
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Letter from the editors. The impact of tropomyosins on actin filament assembly is isoform specific. Geometric control and modeling of genome reprogramming. Post-polymerization crosstalk between the actin cytoskeleton and microtubule network. Where are the limits of the centrosome?
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