Yuan Guoliang, Hassan Md Mahmudul, Yao Tao, Lu Haiwei, Vergara Michael Melesse, Labbé Jesse L, Muchero Wellington, Pan Changtian, Chen Jin-Gui, Tuskan Gerald A, Qi Yiping, Abraham Paul E, Yang Xiaohan
Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
The Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
ACS Synth Biol. 2021 Dec 17;10(12):3600-3603. doi: 10.1021/acssynbio.1c00455. Epub 2021 Dec 8.
CRISPR/Cas has recently emerged as the most reliable system for genome engineering in various species. However, concerns about risks associated with the CRISPR/Cas technology are increasing on potential unintended DNA changes that might accidentally arise from CRISPR gene editing. Developing a system that can detect and report the presence of active CRISPR/Cas tools in biological systems is therefore very necessary. Here, we developed four real-time detection systems that can spontaneously indicate the presence of active CRISPR-Cas tools for genome editing and gene regulation including CRISPR/Cas9 nuclease, base editing, prime editing, and CRISPRa in plants. Using the fluorescence-based molecular biosensors, we demonstrated that the activities of CRISPR/Cas9 nuclease, base editing, prime editing, and CRISPRa can be effectively detected in transient expression via protoplast transformation and leaf infiltration (in , poplar, and tobacco) and stable transformation in .
CRISPR/Cas最近已成为各种物种中基因组工程最可靠的系统。然而,由于CRISPR基因编辑可能意外产生潜在的非预期DNA变化,人们对与CRISPR/Cas技术相关的风险的担忧日益增加。因此,开发一种能够检测并报告生物系统中活性CRISPR/Cas工具存在的系统非常必要。在此,我们开发了四种实时检测系统,它们能够自发地指示用于基因组编辑和基因调控的活性CRISPR-Cas工具的存在,包括植物中的CRISPR/Cas9核酸酶、碱基编辑、引导编辑和CRISPRa。使用基于荧光的分子生物传感器,我们证明了通过原生质体转化和叶片浸润(在拟南芥、杨树和烟草中)进行瞬时表达以及在水稻中进行稳定转化时,可以有效检测CRISPR/Cas9核酸酶、碱基编辑、引导编辑和CRISPRa的活性。