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Borealin 与微管的结合为一种不依赖张力的动粒-微管错误修正途径提供了基础。

The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway.

机构信息

Department of Cell Biology, University of Virginia, Charlottesville, 22908, VA, USA.

Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, 19104, PA, USA.

出版信息

Nat Commun. 2019 Feb 8;10(1):682. doi: 10.1038/s41467-019-08418-4.

Abstract

Proper chromosome segregation depends upon kinetochore phosphorylation by the Chromosome Passenger Complex (CPC). Current models suggest the activity of the CPC decreases in response to the inter-kinetochore stretch that accompanies the formation of bi-oriented microtubule attachments, however little is known about tension-independent CPC phosphoregulation. Microtubule bundles initially lie in close proximity to inner centromeres and become depleted by metaphase. Here we find these microtubules control kinetochore phosphorylation by the CPC in a tension independent manner via a microtubule-binding site on the Borealin subunit. Disruption of Borealin-microtubule interactions generates reduced phosphorylation of prometaphase kinetochores, improper kinetochore-microtubule attachments and weakened spindle checkpoint signals. Experimental and modeling evidence suggests that kinetochore phosphorylation is greatly stimulated when the CPC binds microtubules that lie near the inner centromere, even if kinetochores have high inter-kinetochore stretch. We propose the CPC senses its local environment through microtubule structures to control phosphorylation of kinetochores.

摘要

正确的染色体分离依赖于着丝粒激酶复合物(CPC)对动粒的磷酸化。目前的模型表明,CPC 的活性会随着伴随双定向微管附着形成的动粒间拉伸而降低,但关于与张力无关的 CPC 磷酸化调节知之甚少。微管束最初与着丝粒内中心体紧密相邻,并在中期耗尽。在这里,我们发现这些微管通过着丝粒蛋白 Borealin 亚基上的微管结合位点以不依赖张力的方式控制 CPC 对动粒的磷酸化。破坏 Borealin-微管相互作用会导致前期动粒的磷酸化减少、动粒-微管附着不当和纺锤体检查点信号减弱。实验和建模证据表明,当 CPC 结合位于着丝粒内中心体附近的微管时,动粒的磷酸化会大大增强,即使动粒的动粒间拉伸较大。我们提出 CPC 通过微管结构感知其局部环境,以控制动粒的磷酸化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6d1/6368601/18864412a75e/41467_2019_8418_Fig1_HTML.jpg

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