Abstract
PPM1D phosphatase, also called wild-type p53-induced phosphatase 1, promotes tumor development by inactivating the p53 tumor suppressor pathway. RBM38 RNA-binding protein, also called RNPC1 and a target of p53, inhibits p53 messenger RNA (mRNA) translation, which can be reversed by GSK3 protein kinase via phosphorylation of RBM38 at serine 195. Here we showed that ectopic expression of RBM38 increases, whereas knockdown of RBM38 inhibits, PPM1D mRNA translation. Consistent with this, we found that RBM38 directly binds to PPM1D 3′-untranslated region (3′-UTR) and promotes expression of a heterologous reporter gene that carries PPM1D 3′-UTR in a dose-dependent manner. Interestingly, we showed that PPM1D directly interacts with and dephosphorylates RBM38 at serine 195. Furthermore, we showed that PPM1D modulates p53 mRNA translation and p53-dependent growth suppression through dephosphorylation of RBM38. These findings provide evidence that the crosstalk between PPM1D and RBM38, both of which are targets and modulators of p53, has a critical role in p53 expression and activity.
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Acknowledgements
This work is supported in part by NIH grants CA076069, CA081237 and CA121137.
Author Contributions
MZ and EX did the experiments; MZ, EX and JZ analyzed the data; XC supervised the project and analyzed the data; MZ and XC wrote the manuscript. All the authors read and commented on the draft version of the manuscript and approved the final version.
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Zhang, M., Xu, E., Zhang, J. et al. PPM1D phosphatase, a target of p53 and RBM38 RNA-binding protein, inhibits p53 mRNA translation via dephosphorylation of RBM38. Oncogene 34, 5900–5911 (2015). https://doi.org/10.1038/onc.2015.31
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DOI: https://doi.org/10.1038/onc.2015.31