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向导 RNA 引导的 Argonaute 切割进行基因组操作。

Genome manipulation by guide-directed Argonaute cleavage.

机构信息

Division of Chemistry and Chemical Engineering, California Institute of Technology, MC 114-96, 1200 East California Boulevard, Pasadena, CA 91125, USA.

Division of Biology and Biological Engineering, California Institute of Technology, MC 114-96, 1200 East California Boulevard, Pasadena, CA 91125, USA.

出版信息

Nucleic Acids Res. 2023 May 8;51(8):4078-4085. doi: 10.1093/nar/gkad188.

Abstract

Many prokaryotic argonautes (pAgos) mediate DNA interference by using small DNA guides to cleave target DNA. A recent study shows that CbAgo, a pAgo from Clostridium butyricum, induces DNA interference between homologous sequences and generates double-stranded breaks (DSBs) in target DNAs. This mechanism enables the host to defend against invading DNAs such as plasmids and viruses. However, whether such a CbAgo-mediated DNA cleavage is mutagenic remains unexplored. Here we demonstrate that CbAgo, directed by plasmid-encoded guide sequences, can cleave genome target sites and induce chromosome recombination between downstream homologous sequences in Escherichia coli. The recombination rate correlates well with pAgo DNA cleavage activity and the mechanistic study suggests the recombination involves DSBs and RecBCD processing. In RecA-deficient E. coli strain, guide-directed CbAgo cleavage on chromosomes severely impairs cell growth, which can be utilized as counter-selection to assist Lambda-Red recombineering. These findings demonstrate the guide-directed cleavage of pAgo on the host genome is mutagenic and can lead to different outcomes according to the function of the host DNA repair machinery. We anticipate this novel DNA-guided interference to be useful in broader genetic manipulation. Our study also provides an in vivo assay to characterize or engineer pAgo DNA cleavage activity.

摘要

许多原核 Argonautes(pAgos)通过使用小的 DNA 向导来切割靶 DNA 来介导 DNA 干扰。最近的一项研究表明,丁酸梭菌的 pAgo CbAgo 诱导同源序列之间的 DNA 干扰,并在靶 DNA 中产生双链断裂(DSBs)。这种机制使宿主能够抵抗诸如质粒和病毒等入侵 DNA。然而,这种 CbAgo 介导的 DNA 切割是否具有诱变作用尚不清楚。在这里,我们证明了由质粒编码的指导序列指导的 CbAgo 可以切割基因组靶位点,并在大肠杆菌中诱导下游同源序列之间的染色体重组。重组率与 pAgo DNA 切割活性密切相关,并且机制研究表明重组涉及 DSB 和 RecBCD 加工。在缺乏 RecA 的大肠杆菌菌株中,染色体上指导导向的 CbAgo 切割严重损害细胞生长,这可用于辅助 Lambda-Red 重组酶的反向选择。这些发现表明 pAgo 对宿主基因组的指导导向切割具有诱变作用,并根据宿主 DNA 修复机制的功能导致不同的结果。我们预计这种新的 DNA 引导干扰将在更广泛的遗传操作中有用。我们的研究还提供了一种体内测定法来表征或设计 pAgo DNA 切割活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1859/10164581/51840ea1e98d/gkad188fig1.jpg

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