多倍体酵母的染色体分离依赖于Mps1水平的提高。

Régis E Meyer, Ashlea Sartin, Madeline Gish, Jillian Harsha, Emily Wilkie, Dawson Haworth, Rebecca LaVictoire, Isabel Alberola, Olivia Bowles, Hoa H Chuong, Gary J Gorbsky, Dean S Dawson
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引用次数: 0

摘要

染色体数量增加的肿瘤细胞系通常具有相关的Mps1表达增加,并且这些肿瘤比对照细胞系更依赖Mps1活性来生存。Mps1是一种保守的激酶,参与控制有丝分裂和减数分裂中染色体分离的各个方面。非整倍体细胞对Mps1成瘾的机制解释尚不清楚。为了解决这个问题,我们在染色体组增加的酵母细胞中探索了Mps1依赖性。这些实验表明,在酵母中,倍性的增加会导致染色体在有丝分裂纺锤体上定向的延迟和失败。染色体数量增加的酵母细胞被证明容易受到Mps1活性降低的影响。Mps1活性降低的细胞表现出延长的前分裂期,纺锤体更长,染色体定向延迟。Mps1的一个已知作用是在减数分裂中将Bub1募集到动粒。我们发现多倍体酵母细胞的Mps1成瘾部分是由于其在Bub1募集中的作用。总之,这里的实验表明,倍性的增加使细胞更依赖Mps1在纺锤体上定向染色体。这里描述的现象可能与理解为什么超二倍体癌症细胞表现出对Mps1表达的高度依赖以成功进行染色体分离有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Yeast with elevated chromosome numbers are addicted to high levels of Mps1.

Yeast with elevated chromosome numbers are addicted to high levels of Mps1.

Yeast with elevated chromosome numbers are addicted to high levels of Mps1.

Yeast with elevated chromosome numbers are addicted to high levels of Mps1.

Tumor cell lines with elevated chromosome numbers frequently exhibit elevated expression of Mps1. These tumors are also dependent on high Mps1 activity for their survival. Mps1 is a conserved kinase involved in controlling aspects of chromosome segregation in mitosis and meiosis. The mechanistic explanation for the Mps1-addiction of aneuploid cells is unknown. To address this question, we explored Mps1-dependence in yeast cells with increased sets of chromosomes. These experiments revealed that in yeast, increasing ploidy leads to delays and failures in orienting chromosomes on the mitotic spindle. Yeast cells with elevated numbers of chromosomes proved vulnerable to reductions of Mps1 activity. Cells with reduced Mps1 activity exhibit an extended prometaphase with longer spindles and delays in orienting the chromosomes. One known role of Mps1 is in recruiting Bub1 to the kinetochore in meiosis. We found that the Mps1-addiction of polyploid yeast cells is due in part to its role in Bub1 recruitment. Together, the experiments presented here demonstrate that increased ploidy renders cells more dependent on Mps1 for orienting chromosomes on the spindle. The phenomenon described here may be relevant in understanding why high-ploidy cancer cells exhibit elevated reliance on Mps1 expression for successful chromosome segregation.

Author summary: Losing or gaining chromosomes during cell division leads to aneuploidy (an abnormal number of chromosomes) and can contribute to cancer and other diseases. Indeed, most cells in solid tumors carry abnormally elevated numbers of chromosomes. Mps1 is a regulator of the machinery that distributes chromosomes to daughter cells. In tumors with elevated chromosome numbers, the expression of Mps1 is often also elevated. In some aneuploid tumor cell lines these elevated Mps1 levels have been shown to be critical for tumor survival. To determine how cells with higher ploidy become dependent on Mps1, we explored Mps1-dependence in yeast cells with increased numbers of chromosomes. We report that yeast cells with elevated chromosome number are sensitive to reductions Mps1 expression. In cells with high ploidy and reduced levels of Mps1, the progression of the cell cycle is delayed and the ability of the cells to properly orient and segregate their chromosomes on the spindle is greatly reduced.

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