端粒引导的减数分裂染色体运动:结构和功能的最新进展。

C Y Lee, C G Bisig, M N Conrad, Y Ditamo, L Previato de Almeida, M E Dresser, R J Pezza
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引用次数: 4

摘要

酿酒酵母减数分裂前期染色体通过细胞质产生的力移动,并通过位于核膜上的蛋白质复合体转导到端粒。我们知道染色体运动需要肌动蛋白细胞骨架[13,31]和蛋白质Ndj1、Mps3和Csm4。直到最近,连接Ndj1-Mps3与细胞骨架成分的蛋白质的身份还不清楚。也不知道细胞质马达负责与肌动蛋白细胞骨架和外核膜蛋白相互作用的身份。我们最近的工作[36]发现Mps2是连接Ndj1-Mps3与细胞骨架成分的蛋白质;Myo2作为细胞质马达与Mps2相互作用;和Cms4作为Mps2和Myo2相互作用和活性的调节剂(图1)。下面我们提出了Mps2、Csm4和Myo2如何通过LINC复合体提供端粒与肌动蛋白细胞骨架连接的主要连接来促进染色体运动的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Telomere-led meiotic chromosome movements: recent update in structure and function.

In S. cerevisiae prophase meiotic chromosomes move by forces generated in the cytoplasm and transduced to the telomere via a protein complex located in the nuclear membrane. We know that chromosome movements require actin cytoskeleton [13,31] and the proteins Ndj1, Mps3, and Csm4. Until recently, the identity of the protein connecting Ndj1-Mps3 with the cytoskeleton components was missing. It was also not known the identity of a cytoplasmic motor responsible for interacting with the actin cytoskeleton and a protein at the outer nuclear envelope. Our recent work [36] identified Mps2 as the protein connecting Ndj1-Mps3 with cytoskeleton components; Myo2 as the cytoplasmic motor that interacts with Mps2; and Cms4 as a regulator of Mps2 and Myo2 interaction and activities (Figure 1). Below we present a model for how Mps2, Csm4, and Myo2 promote chromosome movements by providing the primary connections joining telomeres to the actin cytoskeleton through the LINC complex.

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