Genome Editing Tools: Need of the Current Era

S. Aslam, S. Khan, Aftab Ahmed, A. Dandekar
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引用次数: 2

Abstract

Genome editing is considered as the most widely used approach of the present era. It had become a basic need of the current micro and molecular biological experiments. Gene engineering finds its widespread applications in medical, industry and agricultural sector. Unlike previous genetic engineering practices to insert or delete a part of genetic material at random place, genome editing allows the precise manipulation of DNA at a specific location. Zinc Finger Nucleases (ZFNs), Transcription Activator like Effector Nucleases (TALENs), Clustered Regularly Interspresed Short Palindromic repeats (CRISPR/Cas system) and meganucleases (recombinases) are the prime tools for editing an organism’s genome. Genome editing tools have an advantage to selectively delete or to integrate specific genes at specific loci. Use of recombinases for specifying site has further reduced time to integrate genes site specifically. Site specific gene stacking by the use of recombinases coupled with ZFNs, TALENs, or CRISPR/Cas genes have paved new pathways to target genes site specifically and to improve germplasm in lesser time than conventional breeding approaches.
基因组编辑工具:当前时代的需要
基因组编辑被认为是当今时代使用最广泛的方法。它已成为当前微分子生物学实验的基本需求。基因工程在医学、工业和农业领域有着广泛的应用。与以往在随机位置插入或删除部分遗传物质的基因工程实践不同,基因组编辑允许在特定位置精确操纵DNA。锌指核酸酶(ZFNs)、转录激活因子样核酸酶(TALENs)、聚集规律交叉短回语重复序列(CRISPR/Cas系统)和巨核酶(重组酶)是编辑生物体基因组的主要工具。基因组编辑工具具有选择性地删除或整合特定位点上的特定基因的优势。使用重组酶来指定位点进一步减少了基因特异性整合的时间。与传统育种方法相比,利用ZFNs、TALENs或CRISPR/Cas基因偶联的重组酶进行位点特异性基因堆叠,为靶向基因位点和在更短的时间内改善种质资源铺平了新的途径。
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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来源期刊
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