Publication | Open Access
RanGTP aids anaphase entry through Ubr5-mediated protein turnover
19
Citations
55
References
2015
Year
Molecular RegulationCell CycleSpindle Assembly CheckpointTranscriptional RegulationSignaling PathwayCell RegulationSac Protein Bub3Ubr5-mediated Protein TurnoverProtein DegradationCell SignalingSecretory PathwayProtein Quality ControlProtein FunctionCell DivisionProtein TransportCell BiologyChromatin FunctionChromatinChromosome DynamicsSignal TransductionMetaphase Rangtp LevelsNatural SciencesCellular BiochemistrySystems BiologyMedicineCell Development
RanGTP is known to regulate the spindle assembly checkpoint (SAC), but the underlying molecular mechanism is unclear. BuGZ stabilizes SAC protein Bub3 through direct interaction and facilitates its mitotic function. Here we show that RanGTP promotes the turnover of BuGZ and Bub3 in metaphase, which in turn facilitates metaphase-to-anaphase transition. BuGZ and Bub3 interact with either importin-β or an E3 ubiquitin ligase, Ubr5. RanGTP promotes the dissociation of importin-β from BuGZ and Bub3 in metaphase. This results in increased binding of BuGZ and Bub3 to Ubr5, leading to ubiquitination and subsequent turnover of both proteins. We propose that elevated metaphase RanGTP levels use Ubr5 to couple overall chromosome congression to SAC silencing.
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