Stable MCC binding to the APC/C is required for a functional spindle assembly checkpoint

24 Citations (Scopus)

Abstract

The spindle assembly checkpoint (SAC) delays progression into anaphase until all chromosomes have aligned on the metaphase plate by inhibiting Cdc20, the mitotic co-activator of the APC/C. Mad2 and BubR1 bind and inhibit Cdc20, thereby forming the mitotic checkpoint complex (MCC), which can bind stably to the APC/C. Whether MCC formation per se is sufficient for a functional SAC or MCC association with the APC/C is required remains unclear. Here, we analyze the role of two conserved motifs in Cdc20, IR and C-Box, in binding of the MCC to the APC/C. Mutants in both motifs assemble the MCC normally, but IR motif integrity is particularly important for stable binding to the APC/C. Cells expressing Cdc20 with a mutated IR motif have a compromised SAC, as uninhibited Cdc20 can compete with the MCC for APC/C binding and activate it. We thus show that stable MCC association with the APC/C is critical for a functional SAC.
Original languageEnglish
JournalE M B O Reports
Volume15
Pages (from-to)264-272
ISSN1469-221X
DOIs
Publication statusPublished - Mar 2014

Fingerprint

Dive into the research topics of 'Stable MCC binding to the APC/C is required for a functional spindle assembly checkpoint'. Together they form a unique fingerprint.

Cite this