CRISPR-based technologies for large DNA insertions

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Authors: Mary Gracen A. Fuller, Matthew Foley, Rodolphe Barrangou
Cited by: 1
References: 87

Abstract

While the advent of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-based technologies has democratized the genesis of precise mutations, there is a need for more sophisticated tools to enable large-scale DNA manipulations, advancing genome editing across medicine, biotechnology, and agriculture. The success of Cas9 and Cas12 has hinged on the generation of precise DNA nicks and double-stranded breaks (DSBs), enabling local sequence mutagenesis, albeit of a limited size range. Emerging effectors combining Cas with other enzymatic functions, such as CRISPR-associated transposons and site-specific recombinases, enable larger integrations. Sophisticated combinations such as programmable addition via site-specific targeting element (PASTE), prime-editing-assisted site-specific integrase gene editing (PASSIGE), and prime-editing-mediated recombination of opportune target (PrimeRoot) expand payload options and DSB-free editing modalities, with translational potential for next-generation crop breeding in sustainable agriculture and the development of gene and cell therapies in personalized medicine.

Fields of Study & Subjects

CRISPR and Genetic Engineering Innovative Microfluidic and Catalytic Techniques Innovation Pluripotent Stem Cells Research

Publication details

Journal / source
Trends in biotechnology
Publisher
Elsevier BV
Publication date
1 May 2026
Language
EN