Cell cycle-dependent degradation of the Saccharomyces cerevisiae spindle motor Cin8p requires APC(Cdh1) and a bipartite destruction sequence

• Published in: Molecular biology of the cell 2001-11, Vol.12 (11), p.3402
• Main Authors: Hildebrandt, E R, Hoyt, M A
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Amino Acids; Anaphase-Promoting Complex-Cyclosome; Cell Cycle; Fungal Proteins - genetics; Fungal Proteins - metabolism; G1 Phase; Kinesin - genetics; Kinesin - metabolism; Ligases - genetics; Ligases - metabolism; Microtubule-Associated Proteins - genetics; Microtubule-Associated Proteins - metabolism; Molecular Sequence Data; Nuclear Localization Signals; Saccharomyces cerevisiae - metabolism; Saccharomyces cerevisiae Proteins; Spindle Apparatus; Ubiquitin-Protein Ligase Complexes; Ubiquitin-Protein Ligases
• ISSN: 1059-1524
• DOI: 10.1091/mbc.12.11.3402

Saccharomyces cerevisiae Cin8p belongs to the BimC family of kinesin-related motor proteins that are essential for spindle assembly. Cin8p levels were found to oscillate in the cell cycle due in part to a high rate of degradation imposed from the end of mitosis through the G1 phase. Cin8p degradation required the anaphase-promoting complex ubiquitin ligase and its late mitosis regulator Cdh1p but not the early mitosis regulator Cdc20p. Cin8p lacks a functional destruction box sequence that is found in the majority of anaphase-promoting complex substrates. We carried out an extensive mutagenesis study to define the cis-acting sequence required for Cin8p degradation in vivo. The C terminus of Cin8p contains two elements required for its degradation: 1) a bipartite destruction sequence composed of a KEN-box plus essential residues within the downstream 22 amino acids and 2) a nuclear localization signal. The bipartite destruction sequence appears in other BimC kinesins as well. Expression of nondegradable Cin8p showed very mild phenotypic effects, with an increase in the fraction of mitotic cells with broken spindles.