Chen Cheng, Li Ya-Wen, Zheng Yuan-Yuan, Li Xiu-Juan, Wu Na, Guo Qi, Shi Tian-Qiong, Huang He
School of Food Science and Pharmaceutical Engineering, Nanjing Normal University, 2 Xuelin Road, Nanjing 210023, People's Republic of China.
College of Marine and Bioengineering, YanCheng Institute of Technology, Yancheng 224057, People's Republic of China.
Biotechnol Adv. 2025 Jan-Feb;78:108481. doi: 10.1016/j.biotechadv.2024.108481. Epub 2024 Nov 22.
Genome engineering is extensively utilized in diverse scientific disciplines, advancing human welfare and addressing various challenges. Numerous genome engineering tools have been developed to modify genomic sequences. Among these, the CRISPR-Cas system has transformed the field and remains the most commonly employed genome-editing tool. However, the CRISPR-Cas system relies on induced double-strand breaks, with editing efficiency often limited by factors such as cell type and homologous recombination, impeding further progress. CRISPR-associated transposons (CASTs) represent programmable mobile genetic elements. CASTs identified as active were developed as CAST systems, which can perform RNA-guided DNA integration and are featured by high precision, programmability, and kilobase-level payload capacity. Moreover, CAST system allows for precise genome modifications independent of host DNA repair mechanisms, addressing the constraints of conventional CRISPR-Cas systems. It expands the genome engineering toolkit and is poised to become a representative of next-generation genome editing tools. This review thoroughly examines the research progress on CASTs, highlighting the current challenges faced in genome engineering based on CASTs, and offering insights into the ongoing development of this transformative technology.
基因组工程在多种科学学科中得到广泛应用,推动人类福祉并应对各种挑战。人们已开发出众多用于修饰基因组序列的基因组工程工具。其中,CRISPR-Cas系统变革了该领域,仍是最常用的基因组编辑工具。然而,CRISPR-Cas系统依赖诱导双链断裂,编辑效率常受细胞类型和同源重组等因素限制,阻碍了进一步发展。CRISPR相关转座子(CASTs)代表可编程的移动遗传元件。被鉴定为具有活性的CASTs被开发成CAST系统,该系统可进行RNA引导的DNA整合,具有高精度、可编程性和千碱基级别的有效载荷能力等特点。此外,CAST系统能够独立于宿主DNA修复机制进行精确的基因组修饰,解决了传统CRISPR-Cas系统存在的限制。它扩展了基因组工程工具包,有望成为下一代基因组编辑工具的代表。本综述全面审视了CASTs的研究进展,突出了基于CASTs的基因组工程目前面临的挑战,并对这一变革性技术的持续发展提供见解。