Interaction of the S-phase cyclin Clb5 with an "RXL" docking sequence in the initiator protein Orc6 provides an origin-localized replication control switch.
Cyclin-dependent kinases are critical regulators of eukaryotic DNA replication. We show that the S-phase cyclin Clb5 binds stably and directly to the origin recognition complex (ORC). This interaction is mediated by an "RXL" target sequence, or "Cy" motif, in the Orc6 subunit that is recognized by the "hydrophobic patch" region ... on Clb5. The Clb5-Orc6 interaction requires replication initiation, and is maintained throughout the remainder of S phase and into M phase. Eliminating the Clb5-Orc6 interaction has no effect on initiation of replication but instead sensitizes cells to lethal overreplication. We propose that Clb5 binding to ORC provides an origin-localized replication control switch that specifically prevents reinitiation at replicated origins.
Mesh Terms:
Amino Acid Sequence, Binding Sites, Cell Cycle Proteins, Cyclin B, DNA Replication, DNA-Binding Proteins, Enzyme Stability, Mutation, Origin Recognition Complex, S Phase, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Two-Hybrid System Techniques
Amino Acid Sequence, Binding Sites, Cell Cycle Proteins, Cyclin B, DNA Replication, DNA-Binding Proteins, Enzyme Stability, Mutation, Origin Recognition Complex, S Phase, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Two-Hybrid System Techniques
Genes Dev.
Date: May. 01, 2004
PubMed ID: 15105375
View in: Pubmed Google Scholar
Download Curated Data For This Publication
19947
Switch View:
- Interactions 3