Abstract
NIPA (Nuclear Interaction Partner of Alk kinase) is an F-box like protein that targets nuclear Cyclin B1 for degradation. Integrity and therefore activity of the SCF NIPA E3 ligase is regulated by cell-cycle-dependent phosphorylation of NIPA, restricting substrate ubiquitination to interphase. Here we show that phosphorylated NIPA is degraded in late mitosis in an APC/C Cdh1-dependent manner. Binding of the unphosphorylated form of NIPA to Skp1 interferes with binding to the APC/C-adaptor protein Cdh1 and therefore protects unphosphorylated NIPA from degradation in interphase. Our data thus define a novel mode of regulating APC/C-mediated ubiquitination. © 2011 von Klitzing et al.
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CITATION STYLE
von Klitzing, C., Huss, R., Illert, A. L., Fröschl, A., Wötzel, S., Peschel, C., … Duyster, J. (2011). APC/C Cdh1-mediated degradation of the F-box protein NIPA is regulated by its association with Skp1. PLoS ONE, 6(12). https://doi.org/10.1371/journal.pone.0028998
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