Tien Van Vu, Ngan Thi Nguyen, Jihae Kim, Jihae Kim, Yeon Woo Sung, Woo Sik Chung, Jae‐Yean Kim, Jae‐Yean Kim
Precise DNA insertion into plant genomes is central to advancing crop improvement and synthetic biology. CRISPR-Cas systems have enabled programmable DNA integration using tools such as gene targeting (GT), prime editing (PE), and recombinase- or transposase-based platforms. These tools are transitioned from theoretical concepts to practical applications, supporting applications like in-locus protein tagging, regulatory element engineering, and multi-gene stacking. Key challenges persist, such as inefficient large-fragment insertion, delivery barriers, and regulatory hurdles. This review traces the evolution from random to CRISPR-Cas-based systems, analyzes current limitations, and discusses emerging solutions paving the way for predictable DNA insertion in modern plant biotechnology. Precise DNA insertion into plant genomes is crucial for breeding new crop cultivars and advancing plant synthetic biology. Here, the authors review the evolution of plant genome editing systems, analyze their limitations, and discuss the solutions to these challenges.