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Patterns of CRISPR/Cas9 activity in plants, animals and microbes

机译:植物,动物和微生物中的CRISPR / CAS9活性的模式

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Summary The CRISPR/Cas9 system and related RNA-guided endonucleases can introduce double-strand breaks (DSBs) at specific sites in the genome, allowing the generation of targeted mutations in one or more genes as well as more complex genomic rearrangements. Modifications of the canonical CRISPR/Cas9 system from Streptococcus pyogenes and the introduction of related systems from other bacteria have increased the diversity of genomic sites that can be targeted, providing greater control over the resolution of DSBs, the targeting efficiency (frequency of on-target mutations), the targeting accuracy (likelihood of off-target mutations) and the type of mutations that are induced. Although much is now known about the principles of CRISPR/Cas9 genome editing, the likelihood of different outcomes is species-dependent and there have been few comparative studies looking at the basis of such diversity. Here we critically analyse the activity of CRISPR/Cas9 and related systems in different plant species and compare the outcomes in animals and microbes to draw broad conclusions about the design principles required for effective genome editing in different organisms. These principles will be important for the commercial development of crops, farm animals, animal disease models and novel microbial strains using CRISPR/Cas9 and other genome-editing tools.
机译:发明内容CRISPR / CAS9系统和相关的RNA引导的内切核酸酶可以在基因组中的特定位点引入双链断裂(DSB),允许在一种或多种基因中产生靶向突变以及更复杂的基因组重排。来自链球菌的典型CRISPR / CAS9系统的修饰和来自其他细菌的相关系统的引入增加了可以靶向的基因组位点的多样性,从分辨率,靶向效率(目标频率(目标频率)提供更大的控制突变),靶向精度(偏离目标突变的可能性)和诱导的突变的类型。虽然现在已经了解了Crispr / Cas9基因组的原则,但不同结果的可能性是依赖于物种,并且依据这种多样性的基础上存在的比较研究很少。在这里,我们批判地分析了不同植物物种中CRISPR / CAS9和相关系统的活动,并比较了动物和微生物的结果,以得出关于不同生物中有效基因组编辑所需的设计原理的广泛结论。这些原则对于使用CRISPR / CAS9和其他基因组编辑工具的作物,农场动物,动物疾病模型和新型微生物菌株的商业发展至关重要。

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