4.5 Article

RB-dependent S-phase response to DNA damage

期刊

MOLECULAR AND CELLULAR BIOLOGY
卷 20, 期 20, 页码 7751-7763

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AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.20.20.7751-7763.2000

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  1. NCI NIH HHS [CA82525, F32 CA082034, CA58320, R01 CA082525, CA82034, R01 CA058320] Funding Source: Medline

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The retinoblastoma tumor suppressor protein (RB) is a potent inhibitor of cell proliferation. RB is expressed throughout the cell cycle, but its antiproliferative activity is neutralized by phosphorylation during the G(1)/S transition. RB plays an essential role in the G(1) arrest induced by a variety of growth inhibitory signals. In this report, RB is shown to also be required for an intra-S-phase response to DNA damage. Treatment with cisplatin, etoposide, or mitomycin C inhibited S-phase progression in Rb+/+ but not in Rb-/- mouse embryo fibroblasts. Dephosphorylation of RB in S-phase cells temporally preceded the inhibition of DNA synthesis. This S-phase dephosphorylation of RB and subsequent inhibition of DNA replication was observed in p21(Cip1)-deficient cells. The induction of the RB-dependent intra-S-phase arrest persisted for days and correlated with a protection against DNA damage-induced cell death. These results demonstrate that RB plays a protective role in response to genotoxic stress by inhibiting cell cycle progression in G(1) and in S phase.

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