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染色体大小、力学、数量、位置取向和极向逐出力对纺锤体准确性的相互影响:一项 3D 计算研究。

Interrelated effects of chromosome size, mechanics, number, location-orientation and polar ejection force on the spindle accuracy: a 3D computational study.

机构信息

Department of Chemistry, University of Massachusetts, Lowell, MA 01854.

Courant Institute for Mathematical Sciences and Department of Biology, New York University, New York, NY 10012.

出版信息

Mol Biol Cell. 2023 May 15;34(6):ar57. doi: 10.1091/mbc.E22-11-0507. Epub 2023 Feb 15.

DOI:10.1091/mbc.E22-11-0507
PMID:36790911
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10208101/
Abstract

The search-and-capture model of spindle assembly has been a guiding principle for understanding prometaphase for decades. The computational model presented allows one to address two questions: how rapidly the microtubule-kinetochore connections are made, and how accurate these connections are. In most previous numerical simulations, the model geometry was drastically simplified. Using the computational platform, we previously introduced a geometrically and mechanically realistic 3D model of the prometaphase mitotic spindle, and used it to evaluate thermal noise and microtubule kinetics effects on the capture of a single chromosome. Here, we systematically investigate how geometry and mechanics affect a spindle assembly's speed and accuracy, including nuanced distinctions between , , and chromosomes. We find that softening of the centromere spring improves accuracy for short chromosome arms, but accuracy disappears for long chromosome arms. Initial proximity of chromosomes to one spindle pole makes assembly accuracy worse, while initial chromosome orientation matters less. Chromokinesins, added onto flexible chromosome arms, allow modeling of the polar ejection force, improving a spindle assembly's accuracy for a single chromosome. However, spindle space crowding by multiple chromosomes worsens assembly accuracy. Our simulations suggest that the complex microtubule network of the early spindle is key to rapid and accurate assembly.

摘要

几十年来,纺锤体组装的搜索-捕获模型一直是理解前期的指导原则。所提出的计算模型允许人们解决两个问题:微管-动粒连接的形成速度有多快,以及这些连接的准确性如何。在大多数先前的数值模拟中,模型几何形状被大大简化。在之前的研究中,我们使用计算平台引入了一个具有几何和机械真实性的前期有丝分裂纺锤体的 3D 模型,并使用它来评估热噪声和微管动力学对单个染色体捕获的影响。在这里,我们系统地研究了几何形状和力学如何影响纺锤体组装的速度和准确性,包括 、 和 染色体之间的细微区别。我们发现,着丝粒弹簧的软化可以提高短染色体臂的准确性,但长染色体臂的准确性会消失。染色体与一个纺锤体极的初始接近会使组装的准确性变差,而初始染色体的方向则不太重要。添加到柔性染色体臂上的染色体运动蛋白可以模拟极射出力,从而提高单个染色体的组装准确性。然而,多个染色体在纺锤体空间中的拥挤会降低组装的准确性。我们的模拟表明,早期纺锤体的复杂微管网络是快速准确组装的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51cc/10208101/95e87abdd7a7/mbc-34-ar57-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51cc/10208101/95e87abdd7a7/mbc-34-ar57-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51cc/10208101/95e87abdd7a7/mbc-34-ar57-g002.jpg

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