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四倍体细胞的多极有丝分裂:p53 的抑制作用和 Mos 的依赖性。

Multipolar mitosis of tetraploid cells: inhibition by p53 and dependency on Mos.

机构信息

INSERM, Villejuif, France.

出版信息

EMBO J. 2010 Apr 7;29(7):1272-84. doi: 10.1038/emboj.2010.11. Epub 2010 Feb 25.

Abstract

Tetraploidy can constitute a metastable intermediate between normal diploidy and oncogenic aneuploidy. Here, we show that the absence of p53 is not only permissive for the survival but also for multipolar asymmetric divisions of tetraploid cells, which lead to the generation of aneuploid cells with a near-to-diploid chromosome content. Multipolar mitoses (which reduce the tetraploid genome to a sub-tetraploid state) are more frequent when p53 is downregulated and the product of the Mos oncogene is upregulated. Mos inhibits the coalescence of supernumerary centrosomes that allow for normal bipolar mitoses of tetraploid cells. In the absence of p53, Mos knockdown prevents multipolar mitoses and exerts genome-stabilizing effects. These results elucidate the mechanisms through which asymmetric cell division drives chromosomal instability in tetraploid cells.

摘要

四倍体可以构成正常二倍体和致癌非整倍体之间的亚稳态中间状态。在这里,我们表明,p53 的缺失不仅允许四倍体细胞的存活,还允许其进行多极不对称分裂,从而产生具有近二倍体染色体含量的非整倍体细胞。当 p53 下调且 Mos 癌基因产物上调时,多极有丝分裂(将四倍体基因组减少到亚四倍体状态)更为频繁。Mos 抑制多余中心体的融合,从而允许四倍体细胞的正常两极有丝分裂。在没有 p53 的情况下,Mos 敲低可防止多极有丝分裂并发挥基因组稳定作用。这些结果阐明了不对称细胞分裂在四倍体细胞中驱动染色体不稳定性的机制。

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