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Concerns regarding 'off-target' activity of genome editing endonucleases

机译:关于“非目标”基因组编辑内切核酸核酸酶活性的担忧

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摘要

Genome editing (GE) tools ensure targeted mutagenesis and sequence -specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of 'off-target' activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the 'off-target' activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail 'off-target' cleavage. Improvement in target specificity and minimizing 'off-target' activity will offer better applications of GE technology in plant biology and crop improvement.
机译:基因组编辑(GE)工具使用广泛的定制内切核酸酶的植物来确保靶向诱变和序列性修饰;即,锌 - 手指核酸酶(ZFN)和转录活化剂,如效应核酸酶(TALENS),以及CRISPR(聚集定期间隙的短语重复)/ CAS(CROP-相关蛋白)系统。其中,近期CRISPR / CAS9已被广泛用于功能基因组和植物遗传修饰。在GE工具的应用中的一个重要令人担忧是发生“偏离目标”活动和诱导突变,这可能妨碍功能分析和基因活性研究。此外,“偏离目标”活动导致未报告或未知,难以检测,产生不可量化的细胞信号和生理效果。在过去几年中,已经开发了几种实验方法来鉴定不希望的突变并缩减“偏移目标”切割。目标特异性的改善和最小化“偏离目标”活动将提供GE技术在植物生物学和作物改进中的更好应用。

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