RB-Dependent S-Phase Response to DNA Damage

Author:

Knudsen Karen E.1,Booth Dana23,Naderi Soheil23,Sever-Chroneos Zvjezdana1,Fribourg Anne F.1,Hunton Irina C.23,Feramisco James R.34,Wang Jean Y. J.23,Knudsen Erik S.1

Affiliation:

1. Department of Cell Biology, University of Cincinnati, Cincinnati, Ohio 45267-0521, 1 and

2. Department of Biology,2

3. Cancer Center, 3 and

4. School of Medicine, 4 University of California, San Diego, La Jolla, California 92093

Abstract

ABSTRACT 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.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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