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USP11 deubiquitinates RAE1 and plays a key role in bipolar spindle formation
journal contributionposted on 2020-09-14, 10:20 authored by Anna Stockum, Ambrosius P Snijders, Goedele N Maertens
Correct segregation of the mitotic chromosomes into daughter cells is a highly regulated process critical to safeguard genome stability. During M phase the spindle assembly checkpoint (SAC) ensures that all kinetochores are correctly attached before its inactivation allows progression into anaphase. Upon SAC inactivation, the anaphase promoting complex/cyclosome (APC/C) E3 ligase ubiquitinates and targets cyclin B and securin for proteasomal degradation. Here, we describe the identification of Ribonucleic Acid Export protein 1 (RAE1), a protein previously shown to be involved in SAC regulation and bipolar spindle formation, as a novel substrate of the deubiquitinating enzyme (DUB) Ubiquitin Specific Protease 11 (USP11). Lentiviral knock-down of USP11 or RAE1 in U2OS cells drastically reduces cell proliferation and increases multipolar spindle formation. We show that USP11 is associated with the mitotic spindle, does not regulate SAC inactivation, but controls ubiquitination of RAE1 at the mitotic spindle, hereby functionally modulating its interaction with Nuclear Mitotic Apparatus protein (NuMA).
Cell Line, TumorCell ProliferationGene Knockdown TechniquesHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsNuclear Matrix-Associated ProteinsNucleocytoplasmic Transport ProteinsProtein BindingSpindle ApparatusSubstrate SpecificityThiolester HydrolasesUbiquitinationPRTLM-ackGeneral Science & Technology