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出芽酵母细胞皮层中的肌动蛋白和隔膜蛋白超微结构。

Actin and septin ultrastructures at the budding yeast cell cortex.

作者信息

Rodal Avital A, Kozubowski Lukasz, Goode Bruce L, Drubin David G, Hartwig John H

机构信息

Department of Biology, Rosenstiel Basic Medical Science Research Center, Brandeis University, Waltham, MA 02454, USA.

出版信息

Mol Biol Cell. 2005 Jan;16(1):372-84. doi: 10.1091/mbc.e04-08-0734. Epub 2004 Nov 3.

Abstract

Budding yeast has been a powerful model organism for studies of the roles of actin in endocytosis and septins in cell division and in signaling. However, the depth of mechanistic understanding that can be obtained from such studies has been severely hindered by a lack of ultrastructural information about how actin and septins are organized at the cell cortex. To address this problem, we developed rapid-freeze and deep-etch techniques to image the yeast cell cortex in spheroplasted cells at high resolution. The cortical actin cytoskeleton assembles into conical or mound-like structures composed of short, cross-linked filaments. The Arp2/3 complex localizes near the apex of these structures, suggesting that actin patch assembly may be initiated from the apex. Mutants in cortical actin patch components with defined defects in endocytosis disrupted different stages of cortical actin patch assembly. Based on these results, we propose a model for actin function during endocytosis. In addition to actin structures, we found that septin-containing filaments assemble into two kinds of higher order structures at the cell cortex: rings and ordered gauzes. These images provide the first high-resolution views of septin organization in cells.

摘要

芽殖酵母一直是一种强大的模式生物,用于研究肌动蛋白在胞吞作用中的作用以及隔膜蛋白在细胞分裂和信号传导中的作用。然而,由于缺乏关于肌动蛋白和隔膜蛋白在细胞皮层中如何组织的超微结构信息,从这些研究中获得的机制理解深度受到了严重阻碍。为了解决这个问题,我们开发了快速冷冻和深度蚀刻技术,以高分辨率对原生质球化细胞中的酵母细胞皮层进行成像。皮层肌动蛋白细胞骨架组装成由短的、交联的细丝组成的锥形或丘状结构。Arp2/3复合物定位于这些结构的顶端附近,这表明肌动蛋白斑的组装可能从顶端开始。在内吞作用中具有明确缺陷的皮层肌动蛋白斑成分的突变体破坏了皮层肌动蛋白斑组装的不同阶段。基于这些结果,我们提出了一个胞吞作用期间肌动蛋白功能的模型。除了肌动蛋白结构外,我们还发现含隔膜蛋白的细丝在细胞皮层组装成两种更高阶的结构:环和有序的网。这些图像提供了细胞中隔膜蛋白组织的首批高分辨率视图。

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