Resumen
Signal transduction within the canonical Wnt/β-catenin pathway drives development and carcinogenesis through programmed or unprogrammed changes in gene transcription. Although the upstream events linked to signal-induced activation of β-catenin in the cytoplasm have been deciphered in considerable detail, much less is known regarding the mechanism by which β-catenin stimulates target gene transcription in the nucleus. Here, we show that β-catenin physically and functionally targets the MED12 subunit in Mediator to activate transcription. The β-catenin transactivation domain bound directly to isolated MED12 and intact Mediator both in vitro and in vivo, and Mediator was recruited to Wnt-responsive genes in a β-catenin- dependent manner. Disruption of the β-catenin/MED12 interaction through dominant-negative interference- or RNA interference-mediated MED12 suppression inhibited β-catenin transactivation in response to Wnt signaling. This study thus identifies the MED12 interface within Mediator as a new component and a potential therapeutic target in the Wnt/β-catenin pathway.
| Idioma original | English (US) |
|---|---|
| Páginas (desde-hasta) | 14066-14075 |
| Número de páginas | 10 |
| Publicación | Journal of Biological Chemistry |
| Volumen | 281 |
| N.º | 20 |
| DOI | |
| Estado | Published - may 19 2006 |
ASJC Scopus subject areas
- Molecular Biology
- Biochemistry
- Cell Biology
Huella
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