A novel motif governs APC-dependent degradation of Drosophila ORC1 in vivo
A novel motif governs APC-dependent degradation of Drosophila ORC1 in vivo
Regulated degradation plays a key role in setting the level of many factors that govern cell cycle progression. In Drosophila, the largest subunit of the origin recognition complex protein 1 (ORC1) is degraded at the end of M phase and throughout much of G1 by anaphase-promoting complexes (APC) activated by Fzr/Cdh1. We show here that none of the previously identified APC motifs targets ORC1 for degradation. Instead, a novel sequence, the O-box, is necessary and sufficient to direct Fzr/Cdh1-dependent polyubiquitylation in vitro and degradation in vivo. The O-box is similar to but distinct from the well characterized D-box. Finally, we show that O-box motifs in two other proteins, Drosophila Abnormal Spindle and Schizosaccharomyces pombe Cut2, contribute to Cdh1-dependent polyubiquitylation in vitro, suggesting that the O-box may mediate degradation of a variety of cell cycle factors.
- Duke University United States
- The University of Texas Southwestern Medical Center United States
- Duke University Hospital United States
- Duke Medical Center United States
- Philips United Kingdom
Ubiquitin, Amino Acid Motifs, G1 Phase, Origin Recognition Complex, Ubiquitin-Protein Ligase Complexes, Cell Cycle Proteins, Anaphase-Promoting Complex-Cyclosome, Cdh1 Proteins, Securin, Schizosaccharomyces, Animals, Drosophila Proteins, Drosophila, Schizosaccharomyces pombe Proteins, Protein Processing, Post-Translational
Ubiquitin, Amino Acid Motifs, G1 Phase, Origin Recognition Complex, Ubiquitin-Protein Ligase Complexes, Cell Cycle Proteins, Anaphase-Promoting Complex-Cyclosome, Cdh1 Proteins, Securin, Schizosaccharomyces, Animals, Drosophila Proteins, Drosophila, Schizosaccharomyces pombe Proteins, Protein Processing, Post-Translational
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