One-step Cre-loxP organism creation by TAx9

The creation of organisms with Cre-loxP conditional gene recombination systems often faces challenges, particularly when creating the initial (F0) generation with both a Cre recombinase and a DNA site flanked by loxP elements (floxed site). The primary reason is that it is difficult to synthesize a single plasmid with both the Cre gene and the floxed site, since Cre-mediated recombination spontaneously occurs when the plasmid is amplified in Escherichia coli bacterial cells. Here, we introduce an artificial nucleic acid sequence TATATATATATATATATA, named TAx9, that enables the integration of both the Cre gene and the floxed site into a single plasmid. TAx9 effectively blocks spontaneous Cre-mediated recombination in E. coli cells. Using this system, we created an F0 generation of transgenic newts and CRISPR-Cas9 knock-in mice with tissue-specific Cre recombination triggered by tamoxifen. TAx9 technology will be a powerful strategy for creating organisms capable of conditional genetic modification in the F0 generation, accelerating various life science research by reducing the time and cost for ultimately establishing and maintaining lines of genetically modified organisms.

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Publication Details

Journal
Communications Biology
Published
2025-03-06
DOI
https://doi.org/10.1038/s42003-025-07759-9
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
0.00

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One-step Cre-loxP organism creation by TAx9

Tomoki Echigoya, Martin Miguel Casco‐Robles, Takuya Shimazaki, Chikafumi Chiba et al.
Communications Biology
CRISPR and Genetic Engineering
article

One-step Cre-loxP organism creation by TAx9

Tomoki Echigoya, Martin Miguel Casco‐Robles, Takuya Shimazaki, Chikafumi Chiba, Fumiaki Maruo, Yuji Murakami, Seiya Mizuno, Satoru Takahashi, Masaya Hirano
article en

Abstract

The creation of organisms with Cre-loxP conditional gene recombination systems often faces challenges, particularly when creating the initial (F0) generation with both a Cre recombinase and a DNA site flanked by loxP elements (floxed site). The primary reason is that it is difficult to synthesize a single plasmid with both the Cre gene and the floxed site, since Cre-mediated recombination spontaneously occurs when the plasmid is amplified in Escherichia coli bacterial cells. Here, we introduce an artificial nucleic acid sequence TATATATATATATATATA, named TAx9, that enables the integration of both the Cre gene and the floxed site into a single plasmid. TAx9 effectively blocks spontaneous Cre-mediated recombination in E. coli cells. Using this system, we created an F0 generation of transgenic newts and CRISPR-Cas9 knock-in mice with tissue-specific Cre recombination triggered by tamoxifen. TAx9 technology will be a powerful strategy for creating organisms capable of conditional genetic modification in the F0 generation, accelerating various life science research by reducing the time and cost for ultimately establishing and maintaining lines of genetically modified organisms.

Communications BiologyVol. 8(1)
University of Tsukuba (JP), Tsukuba University of Technology (JP)
Japan Society for the Promotion of Science
Decent work and economic growth
Openalex Percentile: Top 96%
CRISPR and Genetic Engineering
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