TY - JOUR T1 - Checkpoint signaling and error correction require regulation of the MPS1 T-loop by PP2A-B56 JF - bioRxiv DO - 10.1101/626937 SP - 626937 AU - Daniel Hayward AU - James Bancroft AU - Davinderpreet Mangat AU - Tatiana Alfonso-Pérez AU - Sholto Dugdale AU - Julia McCarthy AU - Francis A. Barr AU - Ulrike Gruneberg Y1 - 2019/01/01 UR - http://biorxiv.org/content/early/2019/05/03/626937.abstract N2 - During mitosis, the formation of microtubule-kinetochore attachments is monitored by the serine/threonine kinase Mono-Polar Spindle 1 (MPS1). MPS1 is recruited to unattached kinetochores where it phosphorylates KNL1, BUB1 and MAD1 to initiate the spindle checkpoint. This arrests the cell cycle until all kinetochores have been stably captured by microtubules. MPS1 also contributes to the error correction process rectifying incorrect kinetochore attachments. MPS1 activity at kinetochores requires auto-phosphorylation at multiple sites including T676 in the activation segment or “T-loop”. We now demonstrate that a BUBR1-bound pool of PP2A-B56 regulates MPS1 T-loop autophosphorylation and hence activation status in mammalian cells. Overriding this regulation using phospho-mimetic mutations in the MPS1 T-loop to generate a constitutively active kinase results in a prolonged mitotic arrest with continuous turn-over of microtubule-kinetochore attachments. Dynamic regulation of MPS1 catalytic activity by kinetochore-localized PP2A-B56 is thus critical for controlled MPS1 activity and timely cell cycle progression. ER -