6FI8

Crystal structure of the IS608 transposase in complex with left end 29-mer DNA hairpin and a 6-mer DNA representing the intact target site: pre-cleavage target capture complex

6FI8 の概要

• エントリーDOI: 10.2210/pdb6fi8/pdb
• 分子名称: Putative transposase, DNA 29-MER (LE29), DNA 6-MER (T6'), ... (5 entities in total)
• 機能のキーワード: dna-binding protein, protein-dna complex, huh motif, dna stem loop, transposition, tnpa transposase, target capture complex, ishp608, dna binding protein
• 由来する生物種: Helicobacter pylori (Campylobacter pylori); 詳細
• タンパク質・核酸の鎖数: 12
• 化学式量合計: 117018.87

構造登録者

Morero, N.R.,Barabas, O. (登録日: 2018-01-17, 公開日: 2018-03-28, 最終更新日: 2024-01-17)

主引用文献

Morero, N.R.,Zuliani, C.,Kumar, B.,Bebel, A.,Okamoto, S.,Guynet, C.,Hickman, A.B.,Chandler, M.,Dyda, F.,Barabas, O.
Targeting IS608 transposon integration to highly specific sequences by structure-based transposon engineering.
Nucleic Acids Res., 46:4152-4163, 2018

PubMed Abstract: Transposable elements are efficient DNA carriers and thus important tools for transgenesis and insertional mutagenesis. However, their poor target sequence specificity constitutes an important limitation for site-directed applications. The insertion sequence IS608 from Helicobacter pylori recognizes a specific tetranucleotide sequence by base pairing, and its target choice can be re-programmed by changes in the transposon DNA. Here, we present the crystal structure of the IS608 target capture complex in an active conformation, providing a complete picture of the molecular interactions between transposon and target DNA prior to integration. Based on this, we engineered IS608 variants to direct their integration specifically to various 12/17-nt long target sites by extending the base pair interaction network between the transposon and the target DNA. We demonstrate in vitro that the engineered transposons efficiently select their intended target sites. Our data further elucidate how the distinct secondary structure of the single-stranded transposon intermediate prevents extended target specificity in the wild-type transposon, allowing it to move between diverse genomic sites. Our strategy enables efficient targeting of unique DNA sequences with high specificity in an easily programmable manner, opening possibilities for the use of the IS608 system for site-specific gene insertions.

PubMed: 29635476
DOI: 10.1093/nar/gky235

実験手法

X-RAY DIFFRACTION (2.598 Å)