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结合斑马鱼与CRISPR/Cas9:迈向更高效的药物发现流程

Combining Zebrafish and CRISPR/Cas9: Toward a More Efficient Drug Discovery Pipeline.

作者信息

Cornet Carles, Di Donato Vincenzo, Terriente Javier

机构信息

ZeClinics SL, PRBB (Barcelona Biomedical Research Park), Barcelona, Spain.

出版信息

Front Pharmacol. 2018 Jul 3;9:703. doi: 10.3389/fphar.2018.00703. eCollection 2018.

DOI:10.3389/fphar.2018.00703
PMID:30018554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6037853/
Abstract

The use of zebrafish larvae in basic and applied research has grown exponentially during the last 20 years. The reasons for this success lay in its specific experimental advantages: on the one hand, the small size, the large number of progeny and the fast life cycle greatly facilitate large-scale approaches while maintaining 3Rs amenability; on the other hand, high genetic and physiological homology with humans and ease of genetic manipulation make zebrafish larvae a highly robust model for understanding human disease. Together, these advantages allow using zebrafish larvae for performing high-throughput research, both in terms of chemical and genetic phenotypic screenings. Therefore, the zebrafish larva as an animal model is placed between more reductionist high-throughput screenings and informative but low-throughput preclinical assays using mammals. However, despite its biological advantages and growing translational validation, zebrafish remains scarcely used in current drug discovery pipelines. In a context in which the pharmaceutical industry is facing a productivity crisis in bringing new drugs to the market, the combined advantages of zebrafish and the CRISPR/Cas9 system, the most powerful technology for genomic editing to date, has the potential to become a valuable tool for streamlining the generation of models mimicking human disease, the validation of novel drug targets and the discovery of new therapeutics. This review will focus on the most recent advances on CRISPR/Cas9 implementation in zebrafish and all their potential uses in biomedical research and drug discovery.

摘要

在过去20年中,斑马鱼幼体在基础研究和应用研究中的使用呈指数级增长。这一成功的原因在于其特定的实验优势:一方面,体型小、后代数量多和生命周期短极大地促进了大规模研究方法的开展,同时保持了对3R原则的适应性;另一方面,与人类的高度遗传和生理同源性以及易于进行基因操作,使斑马鱼幼体成为理解人类疾病的高度可靠模型。这些优势共同使得斑马鱼幼体可用于进行高通量研究,包括化学和基因表型筛选。因此,斑马鱼幼体作为一种动物模型,介于更为简化的高通量筛选和使用哺乳动物进行的信息丰富但低通量的临床前试验之间。然而,尽管斑马鱼具有生物学优势且越来越多地用于转化验证,但在当前的药物发现流程中,其使用仍然很少。在制药行业面临将新药推向市场的生产力危机的背景下,斑马鱼与CRISPR/Cas9系统(迄今为止最强大的基因组编辑技术)的综合优势,有可能成为一种有价值的工具,用于简化模拟人类疾病的模型的生成、新型药物靶点的验证以及新疗法的发现。本综述将聚焦于CRISPR/Cas9在斑马鱼中的应用的最新进展及其在生物医学研究和药物发现中的所有潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a1/6037853/9de260ee15b8/fphar-09-00703-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a1/6037853/9de260ee15b8/fphar-09-00703-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a1/6037853/9de260ee15b8/fphar-09-00703-g001.jpg

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Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish model.急性多sgRNA敲低KEOPS复合体基因可重现稳定敲除斑马鱼模型的小头畸形表型。
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CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing.
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Unraveling the socio-cognitive consequences of KCC2 disruption in zebrafish: implications for neurodevelopmental disorders and therapeutic interventions.揭示斑马鱼中KCC2破坏的社会认知后果:对神经发育障碍和治疗干预的影响。
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