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• W2110109595 abstract "The spindle checkpoint ensures accurate chromosome segregation by monitoring kinetochore-microtubule attachment. Unattached or tensionless kinetochores activate the checkpoint and enhance the production of the mitotic checkpoint complex (MCC) consisting of BubR1, Bub3, Mad2, and Cdc20. MCC is a critical checkpoint inhibitor of the anaphase-promoting complex/cyclosome, a ubiquitin ligase required for anaphase onset. The N-terminal region of BubR1 binds to both Cdc20 and Mad2, thus nucleating MCC formation. The middle region of human BubR1 (BubR1M) also interacts with Cdc20, but the nature and function of this interaction are not understood. Here we identify two critical motifs within BubR1M that contribute to Cdc20 binding and anaphase-promoting complex/cyclosome inhibition: a destruction box (D box) and a phenylalanine-containing motif termed the Phe box. A BubR1 mutant lacking these motifs is defective in MCC maintenance in mitotic human cells but is capable of supporting spindle-checkpoint function. Thus, the BubR1M-Cdc20 interaction indirectly contributes to MCC homeostasis. Its apparent dispensability in the spindle checkpoint might be due to functional duality or redundant, competing mechanisms.The spindle checkpoint protein BubR1 inhibits the anaphase-promoting complex through binding to Cdc20.ResultsWe identify a new Cdc20-binding motif within BubR1 termed the Phe box.ConclusionThe Phe box maintains steady-state levels of BubR1-containing checkpoint complexes in human cells.SignificanceOur study provides key insights into the homeostatic mechanisms of a key spindle checkpoint complex. The spindle checkpoint ensures accurate chromosome segregation by monitoring kinetochore-microtubule attachment. Unattached or tensionless kinetochores activate the checkpoint and enhance the production of the mitotic checkpoint complex (MCC) consisting of BubR1, Bub3, Mad2, and Cdc20. MCC is a critical checkpoint inhibitor of the anaphase-promoting complex/cyclosome, a ubiquitin ligase required for anaphase onset. The N-terminal region of BubR1 binds to both Cdc20 and Mad2, thus nucleating MCC formation. The middle region of human BubR1 (BubR1M) also interacts with Cdc20, but the nature and function of this interaction are not understood. Here we identify two critical motifs within BubR1M that contribute to Cdc20 binding and anaphase-promoting complex/cyclosome inhibition: a destruction box (D box) and a phenylalanine-containing motif termed the Phe box. A BubR1 mutant lacking these motifs is defective in MCC maintenance in mitotic human cells but is capable of supporting spindle-checkpoint function. Thus, the BubR1M-Cdc20 interaction indirectly contributes to MCC homeostasis. Its apparent dispensability in the spindle checkpoint might be due to functional duality or redundant, competing mechanisms.The spindle checkpoint protein BubR1 inhibits the anaphase-promoting complex through binding to Cdc20. We identify a new Cdc20-binding motif within BubR1 termed the Phe box. The Phe box maintains steady-state levels of BubR1-containing checkpoint complexes in human cells." @default.
• W2110109595 created "2016-06-24" @default.
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• W2110109595 date "2015-01-01" @default.
• W2110109595 modified "2023-10-15" @default.
• W2110109595 title "The Cdc20-binding Phe Box of the Spindle Checkpoint Protein BubR1 Maintains the Mitotic Checkpoint Complex During Mitosis" @default.
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• W2110109595 doi "https://doi.org/10.1074/jbc.m114.616490" @default.
• W2110109595 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4303692" @default.
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