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Updated: Oct 18, 2025

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CRISPR/Cas9 Ribonucleoprotein-mediated Precise Gene Editing by Tube Electroporation
Published on: June 20, 2019
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No apparent p53 activation in CRISPR-engineered gene-edited rabbits
Journal of Cellular and Molecular Medicine
|October 5, 2021
Summary
Gene editing with CRISPR-Cas9 and base editors does not activate the p53 stress response in rabbits. This finding suggests p53 is not a concern for gene-edited animal applications.
Area of Science:
- Molecular Biology
- Genetics
- Biotechnology
Background:
- CRISPR-Cas9 and base editors (BEs) are advanced gene-editing tools with broad applications.
- Previous studies indicated CRISPR-Cas9 can trigger p53-mediated stress responses and cell cycle arrest in human cells.
- This p53 activation has not been observed in gene-edited animals.
Purpose of the Study:
- To investigate whether CRISPR-Cas9 and base editor technologies induce p53 activation in gene-edited animals.
- To provide the first evidence regarding p53 expression changes in gene-edited rabbits.
Main Methods:
- Analysis of p53 expression in nine rabbits generated using CRISPR-Cas9 and base editors.
- Comparative assessment of p53 levels in gene-edited versus control subjects (implied).
Main Results:
- No significant changes in p53 expression were detected in rabbits edited with CRISPR-Cas9 or base editors.
- The study provides the first evidence against p53 activation in gene-edited rabbits.
Conclusions:
- CRISPR-Cas9 and base editor applications in rabbits do not appear to activate the p53 pathway.
- p53 activation is likely not a critical factor to consider for gene editing in animal models.
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