Inhibition of DNA replication factor RPA by p53
- 2 September 1993
- journal article
- research article
- Published by Springer Nature in Nature
- Vol. 365 (6441) , 79-82
- https://doi.org/10.1038/365079a0
Abstract
THE tumour suppressor p53 specifically interferes with the onset of S phase. The mechanism of the growth suppression action of the protein is unclear, though recent evidence points to transcriptional activation and repression functions of the protein1. A competing hypothesis suggests that p53 interacts with the DNA replication apparatus and directly interferes with DNA replication. The major evidence for this hypothesis is that p53 interacts with the simian virus 40 (SV40)-encoded protein T antigen and interferes with the ability of T antigen to unwind the SV40 origin of DNA replication, and recruit DNA polymerase α to the replication initiation complex2,3. Here we report that p53 physically interacts with and inhibits the function of a cellular DNA replication factor, the single-stranded DNA-binding protein complex RPA.Keywords
This publication has 23 references indexed in Scilit:
- Analysis of a protein-binding domain of p53.Molecular and Cellular Biology, 1993
- p53 function and dysfunctionCell, 1992
- Wild-type p53 is a cell cycle checkpoint determinant following irradiation.Proceedings of the National Academy of Sciences, 1992
- p53 functions as a cell cycle control protein in osteosarcomas.Molecular and Cellular Biology, 1990
- Frequent mutations in the p53 tumor suppressor gene in human leukemia T-cell lines.Molecular and Cellular Biology, 1990
- Binding and unwinding—How T antigen engages the SV40 origin of DNA replicationCell, 1990
- Mutations in the p53 gene occur in diverse human tumour typesNature, 1989
- Initiation of Eukaryotic DNA Replication In VitroAnnual Review of Cell Biology, 1989
- Yeast replication factor-A functions in the unwinding of the SV40 origin of DNA replicationNature, 1989
- The murine p53 protein blocks replication of SV40 DNA in vitro by inhibiting the initiation functions of SV40 large T antigenCell, 1989