Evidence map›Paper›PMID 29635476›Full record

ArticleNucleic acids research2018

Targeting IS608 transposon integration to highly specific sequences by structure-based transposon engineering.

Natalia Rosalía Morero, Cecilia Zuliani, Banushree Kumar, Aleksandra Bebel, Sachi Okamoto, Catherine Guynet, Alison Burgess Hickman, Michael Chandler, Fred Dyda, Orsolya Barabas

Abstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Progresses of transposon research inSynthetic and systems biotechnology · 2026
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Natalia Rosalía MoreroStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
Cecilia ZulianiStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
Banushree KumarStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
Aleksandra BebelStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
Sachi OkamotoStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
Catherine GuynetLaboratoire de Microbiologie et Génétique Moléculaires, Centre National de la Recherche Scientifique, Toulouse Cedex 31062, France.
Alison Burgess HickmanLaboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Michael ChandlerLaboratoire de Microbiologie et Génétique Moléculaires, Centre National de la Recherche Scientifique, Toulouse Cedex 31062, France.
Fred DydaLaboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Orsolya BarabasStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.

Funding

Structure and function of novel prokaryotic DNA transposasesZIADK036154 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI DYDA, FREDERICK · 2009 to 2023
$7.7M
6 · The paper itself

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.

Indexed as

DNA Transposable ElementsBase PairingBase SequenceDNA, BacterialGenetic EngineeringHelicobacter pyloriModels, MolecularNucleic Acid ConformationTransposasesDNA, BacterialDNA Transposable ElementsTransposases

Identifiers

PMID29635476
PMCPMC5934647

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.