Securin degradation is mediated by fzy and fzr, and is required for complete chromatid separation but not for cytokinesis

• Published in: The EMBO journal Vol. 20; no. 4; pp. 792 - 801
• Main Authors: Zur, Amit, Brandeis, Michael
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 15.02.2001; Blackwell Publishing Ltd; Oxford University Press
• Subjects: APC; Cdc20 Proteins; Cdh1 Proteins; Cell Cycle; Cell Cycle Proteins - metabolism; Cell Line; Chromatids; Chromosomes; Cyclin B - metabolism; Cyclin B1; cyclosome; fizzy; fzr protein; fzy protein; Humans; Hydrolysis; Neoplasm Proteins - metabolism; PTTG; Securin; Signal Transduction; sister chromatids; ubiquitination; Yeasts
• ISSN: 0261-4189; 1460-2075; 1460-2075
• DOI: 10.1093/emboj/20.4.792

We have studied the ubiquitination and degradation patterns of the human securin/PTTG protein. We show that, in contrast to budding yeast pds1, securin degradation is catalyzed by both fzy (fizzy/cdc20) and fzr (fizzy‐related/cdh1/hct1). Both fzy and fzr also induce the APC/C to ubiquitinate securin in vitro. Securin degradation is mediated by an RXXL destruction box and a KEN box, and is inhibited only when both sequences are mutated. Interestingly, the non‐degradable securin mutant is also partially ubiquitinated by fzy and fzr in vitro. Expressing the non‐degradable securin mutant in cells frequently resulted in incomplete chromatid separation and gave rise to daughter cells connected by a thin chromatin fiber, presumably of chromosomes that failed to split completely. Strikingly, the mutant securin did not prevent the majority of sister chromatids from separating completely, nor did it prevent mitotic cyclin degradation and cytokinesis. This phenotype, reminiscent of the fission yeast cut (cells untimely torn) phenotype, is reported here for the first time in mammals.