| Literature DB >> 25505175 |
Laura A Diaz-Martinez1, Wei Tian1, Bing Li2, Ross Warrington2, Luying Jia1, Chad A Brautigam3, Xuelian Luo4, Hongtao Yu5.
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.Entities:
Keywords: APC/C; Cell Cycle; Kinetochore; Mitosis; Mitotic Checkpoint Complex; Protein-Protein Interaction; Spindle Checkpoint; Ubiquitylation (Ubiquitination)
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Year: 2014 PMID: 25505175 PMCID: PMC4303692 DOI: 10.1074/jbc.M114.616490
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157