Recent Advancement and Innovations in CRISPR/Cas and CRISPR Related Technologies: A review

Sikandar Khan
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Abstract

CRISPR genome editing technologies have been improving by every passing day. The initial CRISPR/Cas9 technologies, though emerged an improved version of genome editing in competition with TALENS and ZFNs, was nevertheless not free from technical and off-target effects. Technological improvements overtime start addressing issues with original CRISPR/Cas9 technology. The major areas of improvement targeted nucleases and delivery methods. Overtime the nuclease like Cas9 had some modifications like FokI-dCas9, Truncated guide RNAs (tru-gRNAs), Paired Cas9 nickase, Cpf1, Cas6 with Csm/Csr complex and chemically treated Cas9. In terms of delivery methods the improvements came along after almost all methods including viral methods like Recombinant Adeno Associated Viruses (rAAV), Lentivirus (LV), and bacteriophages. The review summarizes various non-viral gene delivery modes including physical methods like electroporation and chemical methods like nano particles, cell-derived membrane vesicles (CMVs) with upgraded developments. The review also compares various modes of delivering CRISPR gene editing machinery.
CRISPR/Cas及CRISPR相关技术的最新进展与创新
CRISPR基因编辑技术日新月异。最初的CRISPR/Cas9技术虽然在与TALENS和zfn的竞争中出现了基因组编辑的改进版本,但仍然没有摆脱技术和脱靶效应。随着时间的推移,技术进步开始解决原始CRISPR/Cas9技术的问题。改进的主要领域是针对核酸酶和递送方法。随着时间的推移,Cas9等核酸酶有一些修饰,如FokI-dCas9、截断的引导rna (tru-gRNAs)、配对的Cas9缺口酶、Cpf1、Cas6与Csm/Csr复合物和化学处理的Cas9。在传递方法方面,几乎所有的方法都得到了改进,包括重组腺相关病毒(rAAV)、慢病毒(LV)和噬菌体等病毒方法。本文综述了各种非病毒基因传递方式,包括电穿孔等物理传递方式和纳米颗粒、细胞源性膜囊(CMVs)等化学传递方式。该综述还比较了传递CRISPR基因编辑机制的各种模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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