Analysis of cyclin D3-cdk4 complexes in fibroblasts expressing and lackingp27(kip1) and p21(cip1)

Our studies examined the effects of p27(kip1) and p21(cip1) on the assembly and activity of cyclin D3-cdk4 complexes and determined the composition of the cyclin D3 pool in cells containing and lacking these cyclin-dependent kinase inhibitors. We found that catalytically active cyclin D3-cdk4 comple xes were present in fibroblasts derived from p27(kip1)-p21(cip1)-null mice and that immunodepletion of extracts of wild-type cells dth antibody to p27 (kip1) and/or p21(cip1) removed cyclin D3 protein but not cyclin D3 associa ted activity. Similar results were observed in experiments assaying cyclin D1-cdk4 activity. Data obtained using mixed cell extracts demonstrated that p27(kip1) interacted with cyclin D3-cdk4 complexes in vitro and that this interaction was paralleled by a loss of cyclin D3-cdk4 activity. In p27(kip 1)-p21(cip1)-deficient cells, the cyclin D3 pool consisted primarily of cyc lin D3 monomers, whereas in mild-type cells, the majority of cyclin D3 mole cules were complexed to cdk4 and either p27(kip1) or p21(cip1) or were mono meric. We conclude that neither p27(kip1) nor p21(cip1) is required for the formation of cyclin D3-cdk4 complexes and that cyclin D3-cdk4 complexes co ntaining p27(kip1) or p21(cip1) are inactive. We suggest that only a minor portion of the total cyclin D3 pool accounts for all of the cyclin D3-cdk4 activity in the cell regardless of whether the cell contains p27(kip1) and p21(cip1).