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前期核周肌动蛋白协调中心体分离和定位,以确保染色体准确分离。

Prophase-Specific Perinuclear Actin Coordinates Centrosome Separation and Positioning to Ensure Accurate Chromosome Segregation.

机构信息

Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton BN19RQ, UK.

GiCentre, Department of Computer Science, City, University of London, London EC1V 0HB, UK.

出版信息

Cell Rep. 2020 May 26;31(8):107681. doi: 10.1016/j.celrep.2020.107681.

Abstract

Centrosome separation in late G2/ early prophase requires precise spatial coordination that is determined by a balance of forces promoting and antagonizing separation. The major effector of centrosome separation is the kinesin Eg5. However, the identity and regulation of Eg5-antagonizing forces is less well characterized. By manipulating candidate components, we find that centrosome separation is reversible and that separated centrosomes congress toward a central position underneath the flat nucleus. This positioning mechanism requires microtubule polymerization, as well as actin polymerization. We identify perinuclear actin structures that form in late G2/early prophase and interact with microtubules emanating from the centrosomes. Disrupting these structures by breaking the interactions of the linker of nucleoskeleton and cytoskeleton (LINC) complex with perinuclear actin filaments abrogates this centrosome positioning mechanism and causes an increase in subsequent chromosome segregation errors. Our results demonstrate how geometrical cues from the cell nucleus coordinate the orientation of the emanating spindle poles before nuclear envelope breakdown.

摘要

中心体在晚 G2/早前期的分离需要精确的空间协调,这种协调由促进和拮抗分离的力的平衡决定。中心体分离的主要效应物是驱动蛋白 Eg5。然而,Eg5 拮抗力的身份和调节作用还不太清楚。通过操纵候选成分,我们发现中心体分离是可逆的,并且分离的中心体向核下的中心位置聚集。这种定位机制需要微管聚合以及肌动蛋白聚合。我们发现核周肌动蛋白结构在晚 G2/早前期形成,并与从中心体发出的微管相互作用。通过破坏核骨架和细胞骨架(LINC)复合体与核周肌动蛋白丝的连接来破坏这些结构,会破坏这种中心体定位机制,并导致随后的染色体分离错误增加。我们的结果表明,细胞核的几何线索如何在核膜破裂前协调纺锤体极的发射方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a02c/7262599/af3540c36416/fx1.jpg

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