Department of Internal Medicine ΙΙΙ, Technical University of Munich, Munich, Germany.
PLoS One. 2011;6(12):e28998. doi: 10.1371/journal.pone.0028998. Epub 2011 Dec 20.
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.
NIPA(Alk 激酶的核相互作用伙伴)是一种 F-box 样蛋白,可将核细胞周期蛋白 B1 靶向降解。SCF(NIPA)E3 连接酶的完整性和活性受到 NIPA 的细胞周期依赖性磷酸化调节,从而将底物泛素化限制在细胞间期中。在这里,我们表明磷酸化的 NIPA 在后期有丝分裂中以 APC/C(Cdh1)依赖性方式降解。NIPA 的未磷酸化形式与 Skp1 的结合干扰与 APC/C 衔接蛋白 Cdh1 的结合,从而保护未磷酸化的 NIPA 免受细胞间期的降解。因此,我们的数据定义了一种调节 APC/C 介导的泛素化的新方式。