APC/CFZR-1 Controls SAS-5 Levels To Regulate Centrosome Duplication in <i>Caenorhabditis elegans</i>

Abstract

As the primary microtubule-organizing center, centrosomes play a key role in establishing mitotic bipolar spindles that secure correct transmission of genomic content. For the fidelity of cell division, centrosome number must be strictly controlled by duplicating only once per cell cycle. Proper levels of centrosome proteins are shown to be critical for normal centrosome number and function. Overexpressing core centrosome factors leads to extra centrosomes, while depleting these factors results in centrosome duplication failure. In this regard, protein turnover by the ubiquitin-proteasome system provides a vital mechanism for the regulation of centrosome protein levels. Here, we report that FZR-1, the <i>Caenorhabditis elegans</i> homolog of Cdh1/Hct1/Fzr, a coactivator of the anaphase promoting complex/cyclosome (APC/C), an E3 ubiquitin ligase, functions as a negative regulator of centrosome duplication in the <i>C. elegans</i> embryo. During mitotic cell division in the early embryo, FZR-1 is associated with centrosomes and enriched at nuclei. Loss of <i>fzr-1</i> function restores centrosome duplication and embryonic viability to the hypomorphic <i>zyg-1(it25)</i> mutant, in part, through elevated levels of SAS-5 at centrosomes. Our data suggest that the APC/C^FZR-1 regulates SAS-5 levels by directly recognizing the conserved KEN-box motif, contributing to proper centrosome duplication. Together, our work shows that FZR-1 plays a conserved role in regulating centrosome duplication in <i>C. elegans</i>.