Polycomb Complex 2 Is Required for E-cadherin Repression by the Snail1 Transcription Factor

Author:

Herranz Nicolás1,Pasini Diego2,Díaz Víctor M.1,Francí Clara1,Gutierrez Arantxa3,Dave Natàlia1,Escrivà Maria1,Hernandez-Muñoz Inma1,Di Croce Luciano3,Helin Kristian2,García de Herreros Antonio14,Peiró Sandra1

Affiliation:

1. Programa de Recerca en Càncer, IMIM-Hospital del Mar, Barcelona, Spain

2. Biotech Research and Innovation Centre (BRIC) and Center for Epigenetics, University of Copenhagen, Copenhagen, Denmark

3. ICREA and Centre de Regulació Genòmica, Barcelona, Spain

4. Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, Barcelona, Spain

Abstract

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.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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