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Publication : Mitogen requirement for cell cycle progression in the absence of pocket protein activity.

First Author  Foijer F Year  2005
Journal  Cancer Cell Volume  8
Issue  6 Pages  455-66
PubMed ID  16338659 Mgi Jnum  J:123444
Mgi Id  MGI:3718308 Doi  10.1016/j.ccr.2005.10.021
Citation  Foijer F, et al. (2005) Mitogen requirement for cell cycle progression in the absence of pocket protein activity. Cancer Cell 8(6):455-66
abstractText  Primary mouse embryonic fibroblasts lacking expression of all three retinoblastoma protein family members (TKO MEFs) have lost the G1 restriction point. However, in the absence of mitogens these cells become highly sensitive to apoptosis. Here, we show that TKO MEFs that survive serum depletion pass G1 but completely arrest in G2. p21CIP1 and p27KIP1 inhibit Cyclin A-Cdk2 activity and sequester Cyclin B1-Cdk1 in inactive complexes in the nucleus. This response is alleviated by mitogen restimulation or inactivation of p53. Thus, our results disclose a cell cycle arrest mechanism in G2 that restricts the proliferative capacity of mitogen-deprived cells that have lost the G1 restriction point. The involvement of p53 provides a rationale for the synergism between loss of Rb and p53 in tumorigenesis.
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