National Centre for Molecular Crop Design, Beijing, 100085, China,
Plant Mol Biol. 2014 Jun;85(3):209-18. doi: 10.1007/s11103-014-0188-7. Epub 2014 Mar 18.
Targeted gene regulation on a genome-wide scale is a powerful strategy for interrogating, perturbing, and engineering cellular systems. Recent advances with the RNA-mediated Cas9 endonuclease derived from clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated proteins (Cas) systems have dramatically transformed our ability to specifically modify intact genomes of diverse cells and organisms. The CRISPR-Cas system has been adapted as an efficient, facile, and robust gene-targeting technology with the potential for high-throughput and multiplexed genome engineering. Exciting breakthroughs in understanding the mechanisms of the CRISPR-Cas system and its enormous potential for applications across basic science, agricultural and biotechnology.
在全基因组范围内进行靶向基因调控是一种强大的策略,可以用于研究、干扰和工程化细胞系统。最近,源自成簇规律间隔短回文重复(CRISPR)/CRISPR 相关蛋白(Cas)系统的 RNA 介导的 Cas9 内切酶的进展极大地改变了我们特异性修饰各种细胞和生物体完整基因组的能力。CRISPR-Cas 系统已被改编为一种高效、简便和强大的基因靶向技术,具有高通量和多重基因组工程的潜力。对 CRISPR-Cas 系统的机制及其在基础科学、农业和生物技术等领域的广泛应用的巨大潜力的理解取得了令人兴奋的突破。