Repression of PTEN phosphatase by Snail1 transcriptional factor during gamma radiation-induced apoptosis.

Document Type

Article

Publication Date

2008

Keywords

Apoptosis, Cell-Line, Cell-Line-Tumor, Chromatin-Immunoprecipitation, DNA-Damage, DNA-Complementary, Dogs, G2-Phase, Gamma-Rays, Gene-Expression-Regulation, Genes-Reporter, Humans, Luciferases-Firefly, Luciferases-Renilla, Luminescent-Agents, PTEN-Phosphohydrolase, Pancreatic-Neoplasms, Promoter-Regions-(Genetics), Protein-Synthesis-Inhibitors, Proto-Oncogene-Proteins-c-akt, Puromycin, RNA-Messenger, RNA-Small-Interfering, Selection-(Genetics), Time-Factors, Transcription-Factors, Transfection

First Page

1528

Last Page

1540

JAX Source

Mol Cell Biol 2008 Mar; 28(5):1528-40.

Abstract

The product of the Snail1 gene is a transcriptional repressor required for triggering the epithelial-to-mesenchymal transition. Furthermore, ectopic expression of Snail1 in epithelial cells promotes resistance to apoptosis. In this study, we demonstrate that this resistance to gamma radiation-induced apoptosis caused by Snail1 is associated with the inhibition of PTEN phosphatase. In MDCK cells, mRNA levels of the p53 target gene PTEN are induced after gamma radiation; the transfection of Snail1 prevents this up-regulation. Decreased mRNA levels of PTEN were also detected in RWP-1 cells after the ectopic expression of this transcriptional factor. Snail1 represses and associates to the PTEN promoter as detected both by the electrophoretic mobility shift assay and chromatin immunoprecipitation experiments performed with either endogenous or ectopic Snail1. The binding of Snail1 to the PTEN promoter increases after gamma radiation, correlating with the stabilization of Snail1 protein, and prevents the association of p53 to the PTEN promoter. These results stress the critical role of Snail1 in the control of apoptosis and demonstrate the regulation of PTEN phosphatase by this transcriptional repressor.

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