High-throughput Genetic Screens Using CRISPR-Cas9 System
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The CRISPR-Cas9 system is a powerful tool for genome engineering, and its programmability and simplicity have enabled various types of gene manipulation such as gene disruption and transcriptional and epigenetic perturbation. Particularly, CRISPR-based pooled libraries facilitate high-throughput screening for functional regulatory elements in the human genome. In this review, we describe recent advances in CRISPR-Cas9 technology and its use in high-throughput genetic screening. We also discuss its potential for drug target discovery and current challenges of this technique in biomedical research.
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Ma J, Lu Z Microorganisms. 2025; 13(1).
PMID: 39858940 PMC: 11767912. DOI: 10.3390/microorganisms13010172.
Kim H, Kweon J, Kim Y Exp Mol Med. 2024; 56(4):861-869.
PMID: 38556550 PMC: 11058232. DOI: 10.1038/s12276-024-01212-3.
Yu S, Zhao R, Zhang B, Lai C, Li L, Shen J Asian J Pharm Sci. 2023; 18(4):100828.
PMID: 37583709 PMC: 10424087. DOI: 10.1016/j.ajps.2023.100828.
Synthetic Vulnerabilities in the KRAS Pathway.
Roman M, Hwang E, Sweet-Cordero E Cancers (Basel). 2022; 14(12).
PMID: 35740503 PMC: 9221492. DOI: 10.3390/cancers14122837.
C/EBPδ-induced epigenetic changes control the dynamic gene transcription of and .
Jauch-Speer S, Herrera-Rivero M, Ludwig N, Veras De Carvalho B, Martens L, Wolf J Elife. 2022; 11.
PMID: 35543413 PMC: 9122501. DOI: 10.7554/eLife.75594.