Browse Articles

Article|07 Jun 2024|OPEN
Advancing PAM-less genome editing in soybean using CRISPR-SpRY 
Xiao Chen1,6 , Zhaohui Zhong2,6 , Xu Tang2,3,6 , Suxin Yang1,4 , Yaohua Zhang1 and Shoudong Wang1 , Yiqian Liu5 , Ye Zhang1,4 , Xuelian Zheng2,3 , Yong Zhang2,3 , , Xianzhong Feng,1,4 ,
1Key Laboratory of Soybean Molecular Design Breeding, National Key Laboratory of Black Soils Conservation and Utilization, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, Changchun 130102, China
2Department of Biotechnology, School of Life Sciences and Technology, Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu 610054, China
3Integrative Science Center of Germplasm Creation in Western China (Chongqing) Science City, Chongqing Key Laboratory of Plant Resource Conservation and Germplasm Innovation, School of Life Sciences, Southwest University, Chongqing 400715, China
4College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100049, China
5College of Life Sciences, Jilin Agricultural University, Changchun 130118, China
6Xiao Chen, Zhaohui Zhong, Xu Tang contributed equally to this work.
*Corresponding author. E-mail: zhangyong916@uestc.edu.cn,fengxianzhong@iga.ac.cn

Horticulture Research 11,
Article number: uhae160 (2024)
doi: https://doi.org/10.1093/hr/uhae160
Views: 1122

Received: 27 Dec 2023
Accepted: 30 May 2024
Published online: 07 Jun 2024

Abstract

Although CRISPR-Cas9 technology has been rapidly applied in soybean genetic improvement, it is difficult to achieve the targeted editing of the specific loci in the soybean complex genome due to the limitations of the classical protospacer adjacent motif (PAM). Here, we developed a PAM-less genome editing system mediated by SpRY in soybean. By performing targeted editing of representative agronomic trait targets in soybean and evaluating the results, we demonstrate that the SpRY protein can achieve efficient targeted mutagenesis at relaxed PAM sites in soybean. Furthermore, the SpRY-based cytosine base editor SpRY-hA3A and the adenine base editor SpRY-ABE8e both can accurately induce C-to-T and A-to-G conversion in soybean, respectively. Thus, our data illustrate that the SpRY toolbox can edit the soybean genomic sequence in a PAM-free manner, breaking restrictive PAM barriers in the soybean genome editing technology system. More importantly, our research enriches soybean genome editing tools, which has important practical application value for precise editing and molecular design in soybean breeding.