Department of Life Sciences, Korea University, Seoul 02841, Korea.
Department of Life Sciences, Korea University, Seoul 02841, Korea; Department of Internal Medicine and Laboratory of Genomics and Translational Medicine, Gachon University College of Medicine, Incheon 21565, Korea.
Mol Cells. 2024 Aug;47(8):100092. doi: 10.1016/j.mocell.2024.100092. Epub 2024 Jul 15.
Reverse genetics offers precise functional insights into genes through the targeted manipulation of gene expression followed by phenotypic assessment. While these approaches have proven effective in model organisms such as Saccharomyces cerevisiae, large-scale genetic manipulations in human cells were historically unfeasible due to methodological limitations. However, recent advancements in functional genomics, particularly clustered regularly interspaced short palindromic repeats (CRISPR)-based screening technologies and next-generation sequencing platforms, have enabled pooled screening technologies that allow massively parallel, unbiased assessments of biological phenomena in human cells. This review provides a comprehensive overview of cutting-edge functional genomic screening technologies applicable to human cells, ranging from short hairpin RNA screens to modern CRISPR screens. Additionally, we explore the integration of CRISPR platforms with single-cell approaches to monitor gene expression, chromatin accessibility, epigenetic regulation, and chromatin architecture following genetic perturbations at the omics level. By offering an in-depth understanding of these genomic screening methods, this review aims to provide insights into more targeted and effective strategies for genomic research and personalized medicine.
反向遗传学通过靶向基因表达的操纵,随后进行表型评估,为基因提供精确的功能见解。虽然这些方法在模式生物如酿酒酵母中已被证明是有效的,但由于方法学的限制,在人类细胞中进行大规模的遗传操作在历史上是不可行的。然而,近年来功能基因组学的进展,特别是基于簇状规律间隔短回文重复(CRISPR)的筛选技术和下一代测序平台,已经实现了高通量筛选技术,允许在人类细胞中大规模并行、无偏地评估生物学现象。本文综述了适用于人类细胞的最新功能基因组筛选技术,范围从短发夹 RNA 筛选到现代的 CRISPR 筛选。此外,我们还探讨了将 CRISPR 平台与单细胞方法相结合,以在基因组水平上进行遗传扰动后,监测基因表达、染色质可及性、表观遗传调控和染色质结构。通过深入了解这些基因组筛选方法,本文旨在为基因组研究和个性化医学提供更有针对性和有效的策略。