4.8 Article

Distinct phosphatases antagonize the p53 response in different phases of the cell cycle

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.1322021111

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  1. Netherlands Genomic Initiative of the Nederlandse organisatie voor Wetenschappelijk Onderzoek (Cancer Genomics Center)
  2. Dutch Cancer Society [UU2009-4478]
  3. National Cancer Institute [R01CA142698]
  4. National Institute of Allergy and Infectious Diseases [R01AI101897-01]
  5. American Cancer Society

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The basic machinery that detects DNA damage is the same throughout the cell cycle. Here, we show, in contrast, that reversal of DNA damage responses (DDRs) and recovery are fundamentally different in G1 and G2 phases of the cell cycle. We find that distinct phosphatases are required to counteract the checkpoint response in G1 vs. G2. Whereas WT p53-induced phosphatase 1 (Wip1) promotes recovery in G2-arrested cells by antagonizing p53, it is dispensable for recovery from a G1 arrest. Instead, we identify phosphoprotein phosphatase 4 catalytic subunit (PP4) to be specifically required for cell cycle restart after DNA damage in G1. PP4 dephosphorylates Krupple-associated box domain-associated protein 1-S473 to repress p53-dependent transcriptional activation of p21 when the DDR is silenced. Taken together, our results show that PP4 and Wip1 are differentially required to counteract the p53-dependent cell cycle arrest in G1 and G2, by antagonizing early or late p53-mediated responses, respectively.

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