清脆的
表观遗传学
免疫系统
生物
计算生物学
基因组编辑
转录组
获得性免疫系统
基因
免疫学
遗传学
基因表达
作者
Erin A. Holcomb,Ashley N. Pearson,Kassidy Mikala Jungles,Akshay Tate,Jadyn G. James,Long Jiang,Amanda K. Huber,Michael D. Green
标识
DOI:10.3389/fimmu.2022.1041451
摘要
CRISPR screening is a powerful tool that links specific genetic alterations to corresponding phenotypes, thus allowing for high-throughput identification of novel gene functions. Pooled CRISPR screens have enabled discovery of innate and adaptive immune response regulators in the setting of viral infection and cancer. Emerging methods couple pooled CRISPR screens with parallel high-content readouts at the transcriptomic, epigenetic, proteomic, and optical levels. These approaches are illuminating cancer immune evasion mechanisms as well as nominating novel targets that augment T cell activation, increase T cell infiltration into tumors, and promote enhanced T cell cytotoxicity. This review details recent methodological advances in high-content CRISPR screens and highlights the impact this technology is having on tumor immunology.
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