Kendrin Is a Novel Substrate for Separase Involved in the Licensing of Centriole Duplication

• DOI: 10.1016/j.cub.2012.03.048
• Publication Date: 2012-04-26T16:17:39Z
• Authors: Kazuhiko Matsuo; Keita Ohsumi; Mari Iwabuchi; Toshio Kawamata; Yoshitaka Ono; Mikiko Takahashi
• Keywords: 0301 basic medicine; Agricultural and Biological Sciences(all); Biochemistry, Genetics and Molecular Biology(all); Xenopus; Mitosis; Cell Cycle Proteins; 03 medical and health sciences; COS Cells; Chlorocebus aethiops; Endopeptidases; Animals; Humans; Calmodulin-Binding Proteins; Separase; Centrioles; HeLa Cells

The centrosome, consisting of a pair of centrioles surrounded by pericentriolar material, directs the formation of bipolar spindles during mitosis. Aberrant centrosome number can promote chromosome instability, which is implicated in tumorigenesis. Thus, centrosome duplication needs to be tightly regulated to occur only once per cell cycle. Separase, a cysteine protease that triggers sister chromatid separation, is involved in centriole disengagement, which licenses centrosomes for the next round of duplication. However, at least two questions remain unsolved: what is the substrate relevant to the disengagement, and how does separase, activated at anaphase onset, act on the disengagement that occurs during late mitosis. Here, we show that kendrin, also named pericentrin, is cleaved by activated separase at a consensus site in vivo and in vitro, and this leads to the delayed release of kendrin from the centrosome later in mitosis. Furthermore, we demonstrate that expression of a noncleavable kendrin mutant suppresses centriole disengagement and subsequent centriole duplication. Based on these results, we propose that kendrin is a novel and crucial substrate for separase at the centrosome, protecting the engaged centrioles from premature disengagement and thereby blocking reduplication until the cell passes through mitosis.