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BUB1 对于纺锤体组装检查点受到损害的人类细胞的存活是必需的。

BUB1 Is Essential for the Viability of Human Cells in which the Spindle Assembly Checkpoint Is Compromised.

机构信息

Oncode Institute, Divisions of Cell Biology and Biochemistry, the Netherlands Cancer Institute, Amsterdam, the Netherlands.

Oncode Institute, Divisions of Cell Biology and Biochemistry, the Netherlands Cancer Institute, Amsterdam, the Netherlands.

出版信息

Cell Rep. 2018 Feb 6;22(6):1424-1438. doi: 10.1016/j.celrep.2018.01.034.

Abstract

The spindle assembly checkpoint (SAC) ensures faithful segregation of chromosomes. Although most mammalian cell types depend on the SAC for viability, we found that human HAP1 cells can grow SAC independently. We generated MAD1- and MAD2-deficient cells and mutagenized them to identify synthetic lethal interactions, revealing that chromosome congression factors become essential upon SAC deficiency. Besides expected hits, we also found that BUB1 becomes essential in SAC-deficient cells. We found that the BUB1 C terminus regulates alignment as well as recruitment of CENPF. Second, we found that BUBR1 was not essential in SAC-deficient HAP1 cells. We confirmed that BUBR1 does not regulate chromosome alignment in HAP1 cells and that BUB1 does not regulate chromosome alignment through BUBR1. Taken together, our data resolve some long-standing questions about the interplay between BUB1 and BUBR1 and their respective roles in the SAC and chromosome alignment.

摘要

纺锤体组装检查点 (SAC) 确保染色体的正确分离。虽然大多数哺乳动物细胞类型都依赖 SAC 来维持存活,但我们发现人类 HAP1 细胞可以在没有 SAC 的情况下生长。我们生成了 MAD1 和 MAD2 缺陷细胞,并对其进行诱变以鉴定合成致死相互作用,结果表明 SAC 缺陷时染色体汇聚因子变得必不可少。除了预期的命中外,我们还发现 BUB1 在 SAC 缺陷细胞中变得必不可少。我们发现 BUB1 的 C 端调节着着丝粒的对齐以及 CENPF 的募集。其次,我们发现 BUBR1 在 SAC 缺陷的 HAP1 细胞中不是必需的。我们证实 BUBR1 不会调节 HAP1 细胞中的染色体对齐,并且 BUB1 不会通过 BUBR1 调节染色体对齐。总之,我们的数据解决了一些关于 BUB1 和 BUBR1 之间相互作用及其在 SAC 和染色体对齐中的各自作用的长期存在的问题。

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