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Decoding of methylated histone H3 tail by the Pygo-BCL9 Wnt signaling complex.

Research paper by Marc M Fiedler, María José MJ Sánchez-Barrena, Maxim M Nekrasov, Juliusz J Mieszczanek, Vladimir V Rybin, Jürg J Müller, Phil P Evans, Mariann M Bienz

Indexed on: 24 May '08Published on: 24 May '08Published in: Molecular Cell



Abstract

Pygo and BCL9/Legless transduce the Wnt signal by promoting the transcriptional activity of beta-catenin/Armadillo in normal and malignant cells. We show that human and Drosophila Pygo PHD fingers associate with their cognate HD1 domains from BCL9/Legless to bind specifically to the histone H3 tail methylated at lysine 4 (H3K4me). The crystal structures of ternary complexes between PHD, HD1, and two different H3K4me peptides reveal a unique mode of histone tail recognition: efficient histone binding requires HD1 association, and the PHD-HD1 complex binds preferentially to H3K4me2 while displaying insensitivity to methylation of H3R2. Therefore, this is a prime example of histone tail binding by a PHD finger (of Pygo) being modulated by a cofactor (BCL9/Legless). Rescue experiments in Drosophila indicate that Wnt signaling outputs depend on histone decoding. The specificity of this process provided by the Pygo-BCL9/Legless complex suggests that this complex facilitates an early step in the transition from gene silence to Wnt-induced transcription.