Division of Developmental Biology, Center for Stem Cell & Organoid Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH 45229, USA.
Division of Developmental Biology, Center for Stem Cell & Organoid Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH 45229, USA.
STAR Protoc. 2024 Sep 20;5(3):103221. doi: 10.1016/j.xpro.2024.103221. Epub 2024 Jul 31.
Inducible loss-of-function strategies are crucial for understanding gene function. However, creating inducible, multiple-gene knockout models is challenging and time-consuming. Here, we present a protocol for establishing a doxycycline-inducible CRISPR interference (CRISPRi) system to concurrently silence multiple genes in human induced pluripotent stem cells (hPSCs). We describe the steps for establishing host CRISPRi hPSCs, designing and cloning single-guide RNAs (sgRNAs) into a lentivirus plasmid, and establishing monoclonal CRISPRi hPSC lines transduced with sgRNAs. We also detail the procedures for selecting effective CRISPRi clones. For complete details on the use and execution of this protocol, please refer to Matsui et al..
诱导型基因功能丧失策略对于理解基因功能至关重要。然而,构建诱导型、多基因敲除模型具有挑战性且耗时。本研究提供了一种建立四环素诱导的 CRISPR 干扰(CRISPRi)系统的方案,以在人诱导多能干细胞(hPSC)中同时沉默多个基因。我们描述了建立宿主 CRISPRi hPSC、设计和将单向导 RNA(sgRNA)克隆到慢病毒质粒中以及建立转导 sgRNA 的单克隆 CRISPRi hPSC 系的步骤。我们还详细介绍了筛选有效 CRISPRi 克隆的程序。有关该方案使用和实施的完整详细信息,请参考 Matsui 等人的研究。