Polycomb Complex 2 Is Required for <i>E-cadherin</i> Repression by the Snail1 Transcription Factor

Nicolás Herranz(Municipal Institute for Medical Research), Diego Pasini(University of Copenhagen), Víctor M. Diaz(Hospital Del Mar), Clara Francı́(Municipal Institute for Medical Research), Arantxa Gutiérrez(Centre for Genomic Regulation), Natàlia Dave(Municipal Institute for Medical Research), Maria Escrivà(Hospital Del Mar), Inma Hernandez-Muñoz(Municipal Institute for Medical Research), Luciano Di Croce(Centre for Genomic Regulation), Kristian Helin(University of Copenhagen), Antonio Garcı́a de Herreros(Hospital Del Mar), Sandra Peiró(Hospital Del Mar)
Molecular and Cellular Biology
June 3, 2008
Cited by 421Open Access
Full Text

Abstract

The transcriptional factor Snail1 is a repressor of E-cadherin (CDH1) gene expression essential for triggering epithelial-mesenchymal transition. Snail1 represses CDH1, directly binding its promoter and inducing the synthesis of the Zeb1 repressor. In this article, we show that repression of CDH1 by Snail1, but not by Zeb1, is dependent on the activity of Polycomb repressive complex 2 (PRC2). Embryonic stem (ES) cells null for Suz12, one of the components of PRC2, show higher levels of Cdh1 mRNA than control ES cells. In tumor cells, interference of PRC2 activity prevents the ability of Snail1 to downregulate CDH1 and partially derepresses CDH1. Chromatin immunoprecipitation assays demonstrated that Snail1 increases the binding of Suz12 to the CDH1 promoter and the trimethylation of lysine 27 in histone H3. Moreover, Snail1 interacts with Suz12 and Ezh2, as shown by coimmunoprecipitation experiments. In conclusion, these results demonstrate that Snail1 recruits PRC2 to the CDH1 promoter and requires the activity of this complex to repress E-cadherin expression.


Related Papers

No related papers found

Powered by citation graph analysis