Loughran Allister J, Narina Shilpa, Klein Jonathon, Siwak Jamaica F, Connelly Jon P, Pruett-Miller Shondra M
Center for Advanced Genome Engineering, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Department of Cell & Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Sci Rep. 2025 Apr 17;15(1):13358. doi: 10.1038/s41598-025-96095-3.
Pooled CRISPR screens are vital in the unbiased interrogation of gene function and are instrumental in uncovering therapeutic targets and biological processes. However, follow-up hit validation is critical to confirm observed results. Researchers need a simple and robust approach to rapidly verify putative hits and test resulting observations. Thus, we developed a CRISPR-based method for hit validation that tests the effect of a genetic perturbation on cell fitness. By editing target loci and monitoring the indel profiles over time, we have created a Cellular Fitness (CelFi) assay that can elucidate cellular vulnerabilities and verify hits from pooled CRISPR knockout screens. Unlike traditional cellular fitness assays that evaluate viability over time, the CelFi assay correlates changes in the indel profile at the target gene with a selective growth advantage or disadvantage in individual cells over time. Moreover, the CelFi assay can be utilized to evaluate gene dependencies and test new hypotheses, regardless of variations in single guide RNA optimization, ribonucleoprotein concentration, and gene copy number.
汇集式CRISPR筛选对于无偏向性地探究基因功能至关重要,并且在发现治疗靶点和生物学过程中发挥着重要作用。然而,后续的命中验证对于确认观察结果至关重要。研究人员需要一种简单而稳健的方法来快速验证假定的命中结果并测试所得观察结果。因此,我们开发了一种基于CRISPR的命中验证方法,该方法测试基因扰动对细胞适应性的影响。通过编辑靶位点并随时间监测插入缺失谱,我们创建了一种细胞适应性(CelFi)测定法,该方法可以阐明细胞的脆弱性并验证来自汇集式CRISPR基因敲除筛选的命中结果。与传统的随时间评估活力的细胞适应性测定法不同,CelFi测定法将靶基因处插入缺失谱的变化与单个细胞随时间的选择性生长优势或劣势相关联。此外,无论单向导RNA优化、核糖核蛋白浓度和基因拷贝数存在何种变化,CelFi测定法均可用于评估基因依赖性并测试新的假设。