Gwon Lee Wha, Badon Isabel Wen, Lee Youngjeon, Kim Ho-Joong, Lee Seung Hwan
National Primate Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
KRIBB School of Bioscience, University of Science and Technology, Daejeon, Republic of Korea.
Exp Mol Med. 2025 Sep 1. doi: 10.1038/s12276-025-01530-0.
In recent years, DNA engineering technology has undergone significant advancements, with clustered regularly interspaced short palindromic repeats (CRISPR)-based target-specific DNA insertion emerging as one of the most rapidly expanding and widely studied approaches. Traditional DNA insertion technologies employing recombinases typically involve introducing foreign DNA into genes in vivo by either pre-engineering recognition sequences specific to the recombinase or through genetic crossing to incorporate the requisite recognition sequence into the target gene. However, CRISPR-based gene insertion technologies have advanced to streamline this engineering process by combining the CRISPR-Cas module with recombinase enzymes. This process enables accurate and efficient one-step insertion of foreign DNA into the target gene in vivo. Here we provide an overview of the latest developments in CRISPR-based gene insertion technologies and discusses their potential future applications.
近年来,DNA工程技术取得了重大进展,基于成簇规律间隔短回文重复序列(CRISPR)的靶向特异性DNA插入技术已成为发展最迅速、研究最广泛的方法之一。传统的利用重组酶的DNA插入技术通常涉及通过预先设计重组酶特异性识别序列或通过基因杂交将所需识别序列整合到靶基因中,从而在体内将外源DNA引入基因。然而,基于CRISPR的基因插入技术通过将CRISPR-Cas模块与重组酶结合,改进了这一工程过程。该过程能够在体内将外源DNA准确、高效地一步插入到靶基因中。在此,我们概述了基于CRISPR的基因插入技术的最新进展,并讨论了它们未来可能的应用。