CRISPR-Cas技术作为一种革命性的基因组编辑工具:机制和生物医学应用。

Q2 Biochemistry, Genetics and Molecular Biology
Iranian Biomedical Journal Pub Date : 2023-09-01 Epub Date: 2023-06-18 DOI:10.61186/ibj.27.5.219
S Ebrahimi, Mohammad Ali Khosravi, Abbasali Raz, Morteza Karimipoor, Parviz Parvizi
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引用次数: 0

摘要

可编程核酸酶是用于精确基因组编辑的强大基因组工具。这些工具精确识别、去除或改变特定位点的DNA,从而刺激细胞DNA修复途径,从而导致突变或序列的准确替换或缺失/插入。CRISPR-Cas9系统是最有效和有用的基因组编辑技术,适用于某些细菌和古菌对病毒和噬菌体的防御免疫系统。在过去的十年里,这项技术取得了显著的进步,目前,它已被广泛用于基因组操作,以在植物、动物和人类细胞中进行精确的基因编辑。在这篇综述中,我们旨在解释该系统的基本原理、作用机制以及在不同医学领域的应用,重点是寄生虫病的检测和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CRISPR-Cas Technology as a Revolutionary Genome Editing tool: Mechanisms and Biomedical Applications.

Programmable nucleases are powerful genomic tools for precise genome editing. These tools precisely recognize, remove, or change DNA at a defined site, thereby, stimulating cellular DNA repair pathways that can cause mutations or accurate replacement or deletion/insertion of a sequence. CRISPR-Cas9 system is the most potent and useful genome editing technique adapted from the defense immune system of certain bacteria and archaea against viruses and phages. In the past decade, this technology made notable progress, and at present, it has largely been used in genome manipulation to make precise gene editing in plants, animals, and human cells. In this review, we aim to explain the basic principle, mechanisms of action, and applications of this system in different areas of medicine, with emphasizing on the detection and treatment of parasitic diseases.

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来源期刊
Iranian Biomedical Journal
Iranian Biomedical Journal Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
3.20
自引率
0.00%
发文量
42
审稿时长
8 weeks
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