2VP7

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

2VP7 の概要

• エントリーDOI: 10.2210/pdb2vp7/pdb
• 関連するPDBエントリー: 2VPB 2VPD 2VPE 2VPG
• 分子名称: PYGOPUS HOMOLOG 1, B-CELL CLL/LYMPHOMA 9 PROTEIN, SULFATE ION, ... (5 entities in total)
• 機能のキーワード: gene regulation, wnt signaling pathway, wnt signaling complex, chromosomal rearrangement, signaling protein, proto-oncogene, phosphoprotein, pygo phd domain, bcl9 hd1 domain, histone h3k4me2 tail, zinc, nucleus, zinc-finger, metal-binding
• 由来する生物種: HOMO SAPIENS (HUMAN); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 11636.67

構造登録者

Fiedler, M.,Sanchez-Barrena, M.J.,Nekrasov, M.,Mieszczanek, J.,Rybin, V.,Muller, J.,Evans, P.,Bienz, M. (登録日: 2008-02-26, 公開日: 2008-06-17, 最終更新日: 2024-05-08)

主引用文献

Fiedler, M.,Sanchez-Barrena, M.J.,Nekrasov, M.,Mieszczanek, J.,Rybin, V.,Muller, J.,Evans, P.,Bienz, M.
Decoding of Methylated Histone H3 Tail by the Pygo- Bcl9 Wnt Signaling Complex.
Mol.Cell, 30:507-, 2008

PubMed 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.

PubMed: 18498752
DOI: 10.1016/J.MOLCEL.2008.03.011

実験手法

X-RAY DIFFRACTION (1.65 Å)