5XFP

Binary complex of PHF1 and a double stranded DNA

5XFP の概要

• エントリーDOI: 10.2210/pdb5xfp/pdb
• 関連するPDBエントリー: 5XFN 5XFO 5XFQ 5XFR
• 分子名称: PHD finger protein 1, DNA (5'-D(*GP*GP*GP*CP*GP*GP*CP*CP*GP*CP*CP*CP*T)-3'), ZINC ION, ... (5 entities in total)
• 機能のキーワード: phf1, pcl1, dna, transcription-dna complex, transcription/dna
• 由来する生物種: Homo sapiens (Human); 詳細
• 細胞内の位置: Nucleus: O43189
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 122069.72

構造登録者

Wang, Z.,Li, H. (登録日: 2017-04-11, 公開日: 2017-09-13, 最終更新日: 2023-11-22)

主引用文献

Li, H.,Liefke, R.,Jiang, J.,Kurland, J.V.,Tian, W.,Deng, P.,Zhang, W.,He, Q.,Patel, D.J.,Bulyk, M.L.,Shi, Y.,Wang, Z.
Polycomb-like proteins link the PRC2 complex to CpG islands
Nature, 549:287-291, 2017

PubMed Abstract: The Polycomb repressive complex 2 (PRC2) mainly mediates transcriptional repression and has essential roles in various biological processes including the maintenance of cell identity and proper differentiation. Polycomb-like (PCL) proteins, such as PHF1, MTF2 and PHF19, are PRC2-associated factors that form sub-complexes with PRC2 core components, and have been proposed to modulate the enzymatic activity of PRC2 or the recruitment of PRC2 to specific genomic loci. Mammalian PRC2-binding sites are enriched in CG content, which correlates with CpG islands that display a low level of DNA methylation. However, the mechanism of PRC2 recruitment to CpG islands is not fully understood. Here we solve the crystal structures of the N-terminal domains of PHF1 and MTF2 with bound CpG-containing DNAs in the presence of H3K36me3-containing histone peptides. We show that the extended homologous regions of both proteins fold into a winged-helix structure, which specifically binds to the unmethylated CpG motif but in a completely different manner from the canonical winged-helix DNA recognition motif. We also show that the PCL extended homologous domains are required for efficient recruitment of PRC2 to CpG island-containing promoters in mouse embryonic stem cells. Our research provides the first, to our knowledge, direct evidence to demonstrate that PCL proteins are crucial for PRC2 recruitment to CpG islands, and further clarifies the roles of these proteins in transcriptional regulation in vivo.

PubMed: 28869966
DOI: 10.1038/nature23881

実験手法

X-RAY DIFFRACTION (2.3 Å)