Ceasar S Antony, Rajan Vinothkumar, Prykhozhij Sergey V, Berman Jason N, Ignacimuthu S
Division of Plant Biotechnology, Entomology Research Institute, Loyola College, Chennai, India; Centre for Plant Sciences and School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.
Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada.
Biochim Biophys Acta. 2016 Sep;1863(9):2333-44. doi: 10.1016/j.bbamcr.2016.06.009. Epub 2016 Jun 24.
The clustered, regularly interspaced, short palindromic repeat (CRISPR) and CRISPR associated protein 9 (Cas9) system discovered as an adaptive immunity mechanism in prokaryotes has emerged as the most popular tool for the precise alterations of the genomes of diverse species. CRISPR/Cas9 system has taken the world of genome editing by storm in recent years. Its popularity as a tool for altering genomes is due to the ability of Cas9 protein to cause double-stranded breaks in DNA after binding with short guide RNA molecules, which can be produced with dramatically less effort and expense than required for production of transcription-activator like effector nucleases (TALEN) and zinc-finger nucleases (ZFN). This system has been exploited in many species from prokaryotes to higher animals including human cells as evidenced by the literature showing increasing sophistication and ease of CRISPR/Cas9 as well as increasing species variety where it is applicable. This technology is poised to solve several complex molecular biology problems faced in life science research including cancer research. In this review, we highlight the recent advancements in CRISPR/Cas9 system in editing genomes of prokaryotes, fungi, plants and animals and provide details on software tools available for convenient design of CRISPR/Cas9 targeting plasmids. We also discuss the future prospects of this advanced molecular technology.
成簇规律间隔短回文重复序列(CRISPR)及其相关蛋白9(Cas9)系统最初是作为原核生物的一种适应性免疫机制被发现的,如今已成为用于精准改变多种物种基因组的最流行工具。近年来,CRISPR/Cas9系统在基因组编辑领域掀起了一场风暴。它作为一种基因组改变工具广受欢迎,是因为Cas9蛋白与短引导RNA分子结合后能够在DNA中产生双链断裂,而生产这种短引导RNA分子所付出的努力和成本比生产转录激活样效应核酸酶(TALEN)和锌指核酸酶(ZFN)要少得多。正如文献所示,从原核生物到包括人类细胞在内的高等动物等许多物种都已应用了该系统,这表明CRISPR/Cas9技术日益成熟、操作愈发简便,且适用的物种种类也不断增加。这项技术有望解决生命科学研究(包括癌症研究)中面临的几个复杂分子生物学问题。在本综述中,我们重点介绍了CRISPR/Cas9系统在原核生物、真菌、植物和动物基因组编辑方面的最新进展,并详细介绍了可用于方便设计CRISPR/Cas9靶向质粒的软件工具。我们还讨论了这种先进分子技术的未来前景。
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