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Spatiotemporal regulation of mitotic kinase activity underlies the extensive rearrangement of cellular components required for cell division. One highly dynamic mitotic kinase is Aurora-B (AurB), which has multiple roles defined by the changing localisation of the chromosome passenger complex (CPC) as cells progress through mitosis, including regulation of cytokinesis and abscission. Like other mitotic kinases, AurB is a target of the anaphase-promoting complex (APC/C) ubiquitin ligase during mitotic exit, but it is not known if APC/C-mediated destruction plays any specific role in controlling AurB activity. We have examined the contribution of the Cdh1 coactivator-associated APC/C(Cdh1) to the organization of AurB activity as cells exit mitosis and re-enter interphase. We report that APC/C(Cdh1)-dependent proteolysis restricts a cell-cortex-associated pool of active AurB in space and time. In early G1 phase this pool of AurB is found at protrusions associated with cell spreading. AurB retention at the cortex depends on a formin, FHOD1, critically required to organize the cytoskeleton after division. We identify AurB phosphorylation sites in FHOD1 and show that phosphomutant FHOD1 is impaired in post-mitotic assembly of oriented actin cables. We propose that Cdh1 contributes to spatiotemporal organization of AurB activity and that organization of FHOD1 activity by AurB contributes to daughter cell spreading after mitosis.

Original publication




Journal article


Journal of cell science

Publication Date





2845 - 2856


University of Cambridge Department of Genetics, Downing Street, Cambridge CB2 3EH, UK.


Cell Line, Tumor, Cytoskeleton, Humans, Actins, Fetal Proteins, Nuclear Proteins, Ubiquitin, Signal Transduction, Anaphase, G1 Phase, Cell Movement, Gene Expression Regulation, Phosphorylation, Time Factors, Time-Lapse Imaging, Proteolysis, Aurora Kinase B, Cdh1 Proteins, Formins