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6GDS

Holliday Junctions formed from Telomeric DNA

6GDS の概要
エントリーDOI10.2210/pdb6gds/pdb
関連するPDBエントリー6DGH
分子名称Telomeric DNA (5' CTAACCCTAA) 10mer, Telomeric DNA (5'-TTAGGGTTAG)-3') 10mer (2 entities in total)
機能のキーワードholliday junction, homologous recombination, telomeres, alt mechanism, acc structural motif., recombination
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数4
化学式量合計12176.06
構造登録者
Parkinson, G.N.,Haider, S.,Li, P.,Khiali, S.,Munnur, D.,Ramanathan, A. (登録日: 2018-04-24, 公開日: 2018-11-07, 最終更新日: 2024-01-17)
主引用文献Haider, S.,Li, P.,Khiali, S.,Munnur, D.,Ramanathan, A.,Parkinson, G.N.
Holliday Junctions Formed from Human Telomeric DNA.
J. Am. Chem. Soc., 140:15366-15374, 2018
Cited by
PubMed Abstract: Cells have evolved inherent mechanisms, like homologous recombination (HR), to repair damaged DNA. However, repairs at telomeres can lead to genomic instability, often associated with cancer. While most rapidly dividing cells employ telomerase, the others maintain telomere length through HR-dependent alternative lengthening of telomeres (ALT) pathways. Here we describe the crystal structures of Holliday junction intermediates of the HR-dependent ALT mechanism. Using an extended human telomeric repeat, we also report the crystal structure of two Holliday junctions in close proximity, which associate together through strand exchange to form a hemicatenated double Holliday junction. Our combined structural results demonstrate that ACC nucleotides in the C-rich lagging strand (5'-CTAACCCTAA-3') at the telomere repeat sequence constitute a conserved structural feature that constrains crossover geometry and is a preferred site for Holliday junction formation in telomeres.
PubMed: 30376323
DOI: 10.1021/jacs.8b08699
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.95 Å)
構造検証レポート
Validation report summary of 6gds
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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