Wang Bei, Chen Jun-Zhu, Luo Xue-Qun, Wan Guo-Hui, Tang Yan-Lai, Wang Qiao-Ping
Lab of Metabolism and Aging, School of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Shenzhen 518107, PR China.
Department of Pediatrics, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, Guangdong Province, PR China.
Comput Struct Biotechnol J. 2022 Sep 13;20:5076-5084. doi: 10.1016/j.csbj.2022.09.012. eCollection 2022.
Many toxins are life-threatening to both animals and humans. However, specific antidotes are not available for most of those toxins. The molecular mechanisms underlying the toxicology of well-known toxins are not yet fully characterized. Recently, the advance in CRISPR-Cas9 technologies has greatly accelerated the process of revealing the toxic mechanisms of some common toxins on hosts from a genome-wide perspective. The high-throughput CRISPR screen has made it feasible to untangle complicated interactions between a particular toxin and its corresponding targeting tissue(s). In this review, we present an overview of recent advances in molecular dissection of toxins' cytotoxicity by using genome-wide CRISPR screens, summarize the components essential for toxin-specific CRISPR screens, and propose new strategies for future research.
许多毒素对动物和人类都有生命威胁。然而,大多数此类毒素都没有特效解毒剂。知名毒素毒理学的分子机制尚未完全明确。最近,CRISPR-Cas9技术的进展极大地加速了从全基因组角度揭示一些常见毒素对宿主毒性机制的进程。高通量CRISPR筛选使得理清特定毒素与其相应靶组织之间复杂的相互作用成为可能。在本综述中,我们概述了利用全基因组CRISPR筛选在毒素细胞毒性分子剖析方面的最新进展,总结了毒素特异性CRISPR筛选所必需的组件,并提出了未来研究的新策略。