| Literature DB >> 28441529 |
John Maciejowski1, Hauke Drechsler2, Kathrin Grundner-Culemann3, Edward R Ballister4, Jose-Antonio Rodriguez-Rodriguez5, Veronica Rodriguez-Bravo6, Mathew J K Jones5, Emily Foley7, Michael A Lampson4, Henrik Daub3, Andrew D McAinsh2, Prasad V Jallepalli8.
Abstract
The spindle assembly checkpoint kinase Mps1 not only inhibits anaphase but also corrects erroneous attachments that could lead to missegregation and aneuploidy. However, Mps1's error correction-relevant substrates are unknown. Using a chemically tuned kinetochore-targeting assay, we show that Mps1 destabilizes microtubule attachments (K fibers) epistatically to Aurora B, the other major error-correcting kinase. Through quantitative proteomics, we identify multiple sites of Mps1-regulated phosphorylation at the outer kinetochore. Substrate modification was microtubule sensitive and opposed by PP2A-B56 phosphatases that stabilize chromosome-spindle attachment. Consistently, Mps1 inhibition rescued K-fiber stability after depleting PP2A-B56. We also identify the Ska complex as a key effector of Mps1 at the kinetochore-microtubule interface, as mutations that mimic constitutive phosphorylation destabilized K fibers in vivo and reduced the efficiency of the Ska complex's conversion from lattice diffusion to end-coupled microtubule binding in vitro. Our results reveal how Mps1 dynamically modifies kinetochores to correct improper attachments and ensure faithful chromosome segregation.Entities:
Keywords: Mps1; Ska complex; Ska1; kinetochore; mass spectrometry; microtubule; mitosis; mitotic spindle; phosphorylation; protein kinase
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Year: 2017 PMID: 28441529 PMCID: PMC5477644 DOI: 10.1016/j.devcel.2017.03.025
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270