Wei Xing-Yi, Pei Yang, Liu Li, Hamar Péter, Pei De-Sheng
School of Public Health, Chongqing Medical University, Chongqing 400016, China.
Chongqing Miankai Biotechnology Research Institute Co., Ltd., Chongqing 400025, China; Chongqing No.11 Middle School, Chongqing 400061, China.
STAR Protoc. 2025 Mar 21;6(1):103544. doi: 10.1016/j.xpro.2024.103544. Epub 2025 Jan 10.
The recombinase polymerase amplification (RPA)-CRISPR-Cas12a-FQ system enables sensitive detection of environmental DNA (eDNA) in rare fish species. Here, we present a protocol for eDNA amplification and Cas12a for target recognition using RPA. We describe steps for identifying a target site, synthesis and purification of CRISPR RNA (crRNA), and RPA isothermal amplification. We then detail procedures for constructing the eDNA CRISPR-Cas12a detection system and verifying its sensitivity. This protocol offers a high-sensitivity approach for monitoring aquatic biodiversity and conservation efforts, even in low eDNA concentrations. For complete details on the use and execution of this protocol, please refer to Wei et al..
重组酶聚合酶扩增(RPA)-CRISPR-Cas12a-荧光定量系统能够灵敏检测珍稀鱼类物种的环境DNA(eDNA)。在此,我们展示了一种使用RPA进行eDNA扩增及利用Cas12a进行靶标识别的方法。我们描述了识别靶位点、合成与纯化CRISPR RNA(crRNA)以及RPA等温扩增的步骤。接着,我们详细说明了构建eDNA CRISPR-Cas12a检测系统并验证其灵敏度的程序。该方法为监测水生生物多样性及保护工作提供了一种高灵敏度的方法,即使在eDNA浓度较低的情况下也是如此。有关本方法使用和实施的完整详细信息,请参考Wei等人的研究。