Yan Guangbo, Li Xia, Wang Longyu, Wang Fei, Lv Siyuan, Yu Xiaolan, Li Zhongchen, Cui Jiakai, Sun Baotong, Hou Jia, Li Wenqiang, Xie Xiaochen, Zhao Shuai, Zhang Zhiwei, Chen Wanping, Peng Yanhong, Liu Yang, Ma Lixin
State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei 430062, China.
Nucleic Acids Res. 2025 Jun 20;53(12). doi: 10.1093/nar/gkaf561.
Eukaryotic Argonautes (eAgos) have traditionally been characterized by their ability to utilize RNA guides to identify RNA targets, thereby engaging in post-transcriptional gene silencing pathways. While some eAgos have been demonstrated to use DNA guides for RNA cleavage, the ability of eAgos to cleave DNA targets remains unclear. In this study, we characterized CsAgo, an eAgo protein derived from thermophilic eukaryote Chaetomiumsp. MPI-CAGE-AT-0009, demonstrating a novel ability to cleave both DNA and RNA targets in vitro. Guided by short single-stranded DNA (ssDNA) or RNA, CsAgo exhibits robust RNA cleavage activity at 20-90°C in vitro. CsAgo can effectively cleave ssDNA guided by RNA guides at 20-50°C in vitro. Notably, CsAgo can utilize DNA guides to effectively cleave ssDNA, plasmid double-stranded DNA (dsDNA), and linear dsDNA at ≥80°C in vitro. Based on its ability to cleave dsDNA at high temperatures, CsAgo demonstrates versatility and efficacy in simplifying routine cloning workflows. Additionally, we have developed a CsAgo-based nucleic acid detection method based on a Pyrococcus furiosus Ago-mediated nucleic acid detection method, which exhibits a high sensitivity of six copies/reaction. These results suggest that eAgos include that, in theory, can be utilized for potential DNA-targeting applications. This not only enhances our understanding of eAgos but also expands the toolkit for DNA manipulation.
传统上,真核生物中的 Argonaute 蛋白(eAgos)具有利用 RNA 向导来识别 RNA 靶标的能力,从而参与转录后基因沉默途径。虽然已证明一些 eAgos 可使用 DNA 向导进行 RNA 切割,但 eAgos 切割 DNA 靶标的能力仍不明确。在本研究中,我们对 CsAgo 进行了表征,它是一种源自嗜热真核生物 Chaetomiumsp. MPI-CAGE-AT-0009 的 eAgo 蛋白,在体外表现出切割 DNA 和 RNA 靶标的新能力。在短单链 DNA(ssDNA)或 RNA 的引导下,CsAgo 在体外 20 - 90°C 时表现出强大的 RNA 切割活性。CsAgo 在体外 20 - 50°C 时能有效切割由 RNA 向导引导的 ssDNA。值得注意的是,CsAgo 在体外≥80°C 时可利用 DNA 向导有效切割 ssDNA、质粒双链 DNA(dsDNA)和线性 dsDNA。基于其在高温下切割 dsDNA 的能力,CsAgo 在简化常规克隆工作流程方面展现出多功能性和有效性。此外,我们基于激烈火球菌 Ago 介导的核酸检测方法开发了一种基于 CsAgo 的核酸检测方法,该方法具有六个拷贝/反应的高灵敏度。这些结果表明,eAgos 包括理论上可用于潜在 DNA 靶向应用的蛋白。这不仅加深了我们对 eAgos 的理解,还扩展了 DNA 操作的工具集。