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Updated: Jan 8, 2026

Functional Assessment of BRCA1 variants using CRISPR-Mediated Base Editors
Published on: February 28, 2021
Genome editing outside of controlled facilities: A review of plausible futures and risks
Jack A Heinemann1, Tessa C Hiscox1, Caroline Bedin Zanatta2
1Centre for Integrated Research in Biosafety, School of Biological Sciences, University of Canterbury, Christchurch, New Zealand.
Abstract:
Vectors for delivering proteins and/or nucleic acids into the cells of whole organisms, from single to multicellular, are rapidly advancing. Common cargos are nucleic acids needed to express the components of a genome editing reaction, or ribonucleoproteins (RNP) that can act immediately upon delivery. In only 20 years, improvements in associated formulation technologies have decreased the dependence of genome editing on the need for a laboratory or trained personnel, allowing for genome editing outside of controlled facilities. As this happens, both target and non-target organisms may be exposed to active biological agents, necessitating a new framework for risk assessment. Some scientists deny developments for gene editing in uncontrolled environments, leading to scientifically unjustified dismissals of risk.
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