微管生长速率的调控及其对染色体不稳定性的影响。

IF 3.4 3区 生物学 Q3 CELL BIOLOGY
Lia Mara Gomes Paim, Susanne Bechstedt
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引用次数: 0

摘要

微管是α/β微管蛋白二聚体的聚合物,它们构建有丝分裂纺锤体,在细胞分裂过程中分离复制的染色体。微管的功能是由动态不稳定性控制的,因此生长和收缩的周期有助于染色体运动所必需的力量。微管生长速度的调节需要细胞周期依赖性的微管相关蛋白(MAPs)的表达、定位和活性变化,以及调节微管动力学的微管蛋白翻译后修饰。很明显,适当的染色体分离和倍性维持需要最佳的微管生长速度。微管生长速度的次优可能是由于map活性的改变,并可能导致非整倍性,可能是由于破坏了着丝点微管束的建立和改变了姐妹染色单体分离所需的机械力。未来使用高分辨率,低光毒性显微镜和新型荧光标记的工作将在获得微管过程如何促进染色体分离的更深入的机制见解方面具有不可估量的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of microtubule growth rates and their impact on chromosomal instability.

Microtubules are polymers of α/β tubulin dimers that build the mitotic spindle, which segregates duplicated chromosomes during cell division. Microtubule function is governed by dynamic instability, whereby cycles of growth and shrinkage contribute to the forces necessary for chromosome movement. Regulation of microtubule growth velocity requires cell cycle-dependent changes in expression, localization and activity of microtubule-associated proteins (MAPs) as well as tubulin post-translational modifications that modulate microtubule dynamics. It has become clear that optimal microtubule growth velocities are required for proper chromosome segregation and ploidy maintenance. Suboptimal microtubule growth rates can result from altered activity of MAPs and could lead to aneuploidy, possibly by disrupting the establishment of microtubule bundles at kinetochores and altering the mechanical forces required for sister chromatid segregation. Future work using high-resolution, low-phototoxicity microscopy and novel fluorescent markers will be invaluable in obtaining deeper mechanistic insights into how microtubule processes contribute to chromosome segregation.

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来源期刊
Cell Cycle
Cell Cycle 生物-细胞生物学
CiteScore
7.70
自引率
2.30%
发文量
281
审稿时长
1 months
期刊介绍: Cell Cycle is a bi-weekly peer-reviewed journal of high priority research from all areas of cell biology. Cell Cycle covers all topics from yeast to man, from DNA to function, from development to aging, from stem cells to cell senescence, from metabolism to cell death, from cancer to neurobiology, from molecular biology to therapeutics. Our goal is fast publication of outstanding research.
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