PML bodies control the nuclear dynamics and function of the CHFR mitotic checkpoint protein

被引:27
作者
Daniels, MJ
Marson, A
Venkitaraman, AR
机构
[1] Univ Cambridge, Canc Res UK Dept Oncol, Cambridge CB2 2XZ, England
[2] MRC, Canc Cell Unit, Cambridge CB2 2XZ, England
基金
英国医学研究理事会;
关键词
D O I
10.1038/nsmb837
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nuclear foci containing the promyelocytic leukemia protein (PML bodies), which occur in most cells, play a role in tumor suppression. Here, we demonstrate that CHFR, a mitotic checkpoint protein frequently inactivated in human cancers, is a dynamic component of PML bodies. Intermolecular fluorescence resonance energy transfer analysis identified a distinct fraction of CHFR that interacts with PML in living cells. This interaction modulates the nuclear distribution and mobility of CHFR. A trans-dominant mutant of CHFR that inhibits checkpoint function also prevents colocalization and interaction with PML. Conversely, the distribution and mobility of CHFR are perturbed in PML-/- cells, accompanied by aberrations in mitotic entry and the response to spindle depolymerization. Thus, PML bodies control the distribution, dynamics and function of CHFR. Our findings implicate the interaction between these tumor suppressors in a checkpoint response to microtubule poisons, an important class of anticancer drugs.
引用
收藏
页码:1114 / 1121
页数:8
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