Cdk phosphorylation triggers sequential intramolecular interactions that progressively block Rb functions as cells move through G1.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 10499802.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
We present evidence that phosphorylation of the C-terminal region of Rb by Cdk4/6 initiates successive intramolecular interactions between the C-terminal region and the central pocket. The initial interaction displaces histone deacetylase from the pocket, blocking active transcriptional repression by Rb. This facilitates a second interaction that leads to phosphorylation of the pocket by Cdk2 and disruption of pocket structure. These intramolecular interactions provide a molecular basis for sequential phosphorylation of Rb by Cdk4/6 and Cdk2. Cdk4/6 is activated early in G1, blocking active repression by Rb. However, it is not until near the end of G1, when cyclin E is expressed and Cdk2 is activated, that Rb is prevented from binding and inactivating E2F.
Medical subject headings
- CDC2-CDC28 Kinases
- Carrier Proteins
- Cell Cycle Proteins
- Cyclin-Dependent Kinases
- DNA-Binding Proteins
- G1 Phase
- Gene Expression Regulation
- Peptide Fragments
- Proto-Oncogene Proteins
- Retinoblastoma Protein