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锚定启动:基于肌动蛋白的核定位机制

ANChors away: an actin based mechanism of nuclear positioning.

作者信息

Starr Daniel A, Han Min

机构信息

Howard Hughes Medical Institute and Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.

出版信息

J Cell Sci. 2003 Jan 15;116(Pt 2):211-6. doi: 10.1242/jcs.00248.

Abstract

Mechanisms for nuclear migration and nuclear anchorage function together to control nuclear positioning. Both tubulin and actin networks play important roles in nuclear positioning. The actin cytoskeleton has been shown to position nuclei in a variety of systems from yeast to plants and animals. It can either act as a stable skeleton to anchor nuclei or supply the active force to move nuclei. Two C. elegans genes and their homologues play important roles in these processes. Syne/ANC-1 anchors nuclei by directly tethering the nuclear envelope to the actin cytoskeleton, and UNC-84/SUN functions at the nuclear envelope to recruit Syne/ANC-1.

摘要

核迁移和核锚定机制共同作用以控制细胞核定位。微管蛋白和肌动蛋白网络在细胞核定位中都发挥着重要作用。在从酵母到植物和动物的各种系统中,肌动蛋白细胞骨架已被证明可定位细胞核。它既可以作为稳定的骨架来锚定细胞核,也可以提供使细胞核移动的作用力。两种秀丽隐杆线虫基因及其同源物在这些过程中发挥重要作用。Syne/ANC-1通过将核膜直接连接到肌动蛋白细胞骨架来锚定细胞核,而UNC-84/SUN在核膜处发挥作用以招募Syne/ANC-1。

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