摘要
The p27^Kipl protein was initially identified due to its ability to bind and inhibit cyclin/cdk2 complexes leading to an arrest in the G1-phase of the cell cycle. In line with the cyclin kinase inhibitory function of p27, knockout mice show a 30% increase in body size and a higher cyclin kinase activity in thymocytes leading to an accelerated passage through the cell cycle. The generation of p27 knockout mice helped to formally establish p27 function as a tumor suppressor protein.
