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Cited by 158

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Efficient engineering of a bacteriophage genome using the type I-E CRISPR-Cas system

Open access
Kiro, Ruth, Shitrit, Dror, Qimron, Udi·2014·RNA Biology

Abstract

The clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated (Cas) system has recently been used to engineer genomes of various organisms, but surprisingly, not those of bacteriophages (phages). Here we present a method to genetically engineer the Escherichia coli phage T7 using the type I-E CRISPR-Cas system. T7 phage genome is edited by homologous recombination with a DNA sequence flanked by sequences homologous to the desired location. Non-edited genomes are targeted by the CRISPR-Cas system, thus enabling isolation of the desired recombinant phages. This method broadens CRISPR Cas-based editing to phages and uses a CRISPR-Cas type other than type II. The method may be adjusted to genetically engineer any bacteriophage genome.

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Metadata

Authors
Kiro, R., Shitrit, D., & Qimron, U.
Venue
RNA Biology
Published
2014-01-01
Volume
11
Issue
1
Pages
42-44
ISSN
  • 1547-6286 (ISSN-L)
  • 1555-8584
OpenAlex
W2034786222
Cited by
158
References
4
FWCI
3.65
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Efficient engineering of a bacteriophage genome using the type I-E CRISPR-Cas system. https://app.cochat.ai/papers/10.4161/rna.27766
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Kiro, R., Shitrit, D., & Qimron, U. (2014). Efficient engineering of a bacteriophage genome using the type I-E CRISPR-Cas system. RNA Biology. https://doi.org/10.4161/rna.27766

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.