6USJ

Structure of two nucleosomes bridged by human PARP2

6USJ の概要

• エントリーDOI: 10.2210/pdb6usj/pdb
• EMDBエントリー: 20864
• 分子名称: Widom 601 DNA (160-MER), Histone H3.1, Histone H4, ... (7 entities in total)
• 機能のキーワード: parp2, nucleosome, complex, bridging, dna binding protein-dna complex, dna binding protein/dna
• 由来する生物種: synthetic construct; 詳細
• タンパク質・核酸の鎖数: 22
• 化学式量合計: 562132.64

構造登録者

Gaullier, G.,Bowerman, S.,Luger, K. (登録日: 2019-10-27, 公開日: 2020-10-14, 最終更新日: 2024-03-06)

主引用文献

Gaullier, G.,Roberts, G.,Muthurajan, U.M.,Bowerman, S.,Rudolph, J.,Mahadevan, J.,Jha, A.,Rae, P.S.,Luger, K.
Bridging of nucleosome-proximal DNA double-strand breaks by PARP2 enhances its interaction with HPF1.
Plos One, 15:e0240932-e0240932, 2020

PubMed Abstract: Poly(ADP-ribose) Polymerase 2 (PARP2) is one of three DNA-dependent PARPs involved in the detection of DNA damage. Upon binding to DNA double-strand breaks, PARP2 uses nicotinamide adenine dinucleotide to synthesize poly(ADP-ribose) (PAR) onto itself and other proteins, including histones. PAR chains in turn promote the DNA damage response by recruiting downstream repair factors. These early steps of DNA damage signaling are relevant for understanding how genome integrity is maintained and how their failure leads to genome instability or cancer. There is no structural information on DNA double-strand break detection in the context of chromatin. Here we present a cryo-EM structure of two nucleosomes bridged by human PARP2 and confirm that PARP2 bridges DNA ends in the context of nucleosomes bearing short linker DNA. We demonstrate that the conformation of PARP2 bound to damaged chromatin provides a binding platform for the regulatory protein Histone PARylation Factor 1 (HPF1), and that the resulting HPF1•PARP2•nucleosome complex is enzymatically active. Our results contribute to a structural view of the early steps of the DNA damage response in chromatin.

PubMed: 33141820
DOI: 10.1371/journal.pone.0240932

実験手法

ELECTRON MICROSCOPY (10.5 Å)