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Exploiting CRISPR-Cas immune systems for genome editing in bacteria

机译:利用CRISPR-Cas免疫系统进行细菌基因组编辑

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摘要

The CRISPR-Cas immune system is a DNA-encoded, RNA mediated, DNA-targeting defense mechanism, which provides sequence-specific targeting of DNA. This molecular machinery can be engineered into the sgRNA:Cas9 technology, for programmable cleavage of DNA. Following the genesis of double-stranded DNA breaks, the DNA repair machinery generates mutations at the cleavage site using various pathways. This technology has revolutionized eukaryotic genome editing, and we are at the cusp of full exploitation in bacteria. Here, we discuss the potential of CRISPR-based technologies for use in bacteria, and highlight the application of single stranded DNA recombineering combined with CRISPR-Cas selection to edit the genome of a probiotic organism. We envision that CRISPR-Cas technologies will play a key role in the development of next-generation industrial bacteria.
机译:CRISPR-Cas免疫系统是一种DNA编码的,RNA介导的,靶向DNA的防御机制,可提供对DNA的序列特异性靶向。可以将这种分子机制工程化到sgRNA:Cas9技术中,以进行DNA的可编程切割。在双链DNA断裂的产生之后,DNA修复机制会使用各种途径在裂解位点产生突变。这项技术彻底改变了真核生物的基因组编辑,而我们正处于细菌全面开发的风口浪尖。在这里,我们讨论了基于CRISPR的技术在细菌中的应用潜力,并重点介绍了单链DNA重组与CRISPR-Cas选择相结合的应用,以编辑益生菌的基因组。我们设想,CRISPR-Cas技术将在下一代工业细菌的发展中发挥关键作用。

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