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.
Originalsprache | Englisch |
---|---|
Aufsatznummer | e28998 |
Fachzeitschrift | PLoS ONE |
Jahrgang | 6 |
Ausgabenummer | 12 |
DOIs | |
Publikationsstatus | Veröffentlicht - 20 Nov. 2011 |