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描述乳杆菌中丰富、多样且活跃的 CRISPR-Cas 系统的活性。

Characterizing the activity of abundant, diverse and active CRISPR-Cas systems in lactobacilli.

机构信息

North Carolina State University Functional Genomics, Raleigh, NC, 27695, USA.

North Carolina State University Department of Food, Bioprocessing and Nutrition Sciences, Raleigh, NC, 27695, USA.

出版信息

Sci Rep. 2018 Aug 1;8(1):11544. doi: 10.1038/s41598-018-29746-3.

Abstract

CRISPR-Cas systems provide immunity against phages and plasmids in bacteria and archaea. Despite the popularity of CRISPR-Cas9 based genome editing, few endogenous systems have been characterized to date. Here, we sampled 1,262 publically available lactobacilli genomes found them to be enriched with CRISPR-Cas adaptive immunity. While CRISPR-Cas is ubiquitous in some Lactobacillus species, CRISPR-Cas content varies at the strain level in most Lactobacillus species. We identified that Type II is the most abundant type across the genus, with II-A being the most dominant sub-type. We found that many Type II-A systems are actively transcribed, and encode spacers that efficiently provide resistance against plasmid uptake. Analysis of various CRISPR transcripts revealed that guide sequences are highly diverse in terms of crRNA and tracrRNA length and structure. Interference assays revealed highly diverse target PAM sequences. Lastly, we show that these systems can be readily repurposed for self-targeting by expressing an engineered single guide RNA. Our results reveal that Type II-A systems in lactobacilli are naturally active in their native host in terms of expression and efficiently targeting invasive and genomic DNA. Together, these systems increase the possible Cas9 targeting space and provide multiplexing potential in native hosts and heterologous genome editing purpose.

摘要

CRISPR-Cas 系统为细菌和古菌提供了针对噬菌体和质粒的免疫能力。尽管基于 CRISPR-Cas9 的基因组编辑技术非常流行,但迄今为止,只有少数内源性系统得到了描述。在这里,我们对 1262 个公开可用的乳杆菌基因组进行了采样,发现它们富含 CRISPR-Cas 适应性免疫。虽然 CRISPR-Cas 在某些乳杆菌物种中普遍存在,但在大多数乳杆菌物种中,CRISPR-Cas 的含量在菌株水平上存在差异。我们确定 II 型是该属中最丰富的类型,II-A 是最主要的亚型。我们发现许多 II-A 系统被积极转录,并编码间隔序列,有效地提供了对质粒摄取的抗性。对各种 CRISPR 转录本的分析表明,在 crRNA 和 tracrRNA 的长度和结构方面,指导序列具有高度多样性。干扰测定显示出高度多样化的靶 PAM 序列。最后,我们证明这些系统可以通过表达工程化的单指导 RNA 来轻易地重新用于自我靶向。我们的结果表明,乳杆菌中的 II-A 系统在其天然宿主中在表达和靶向入侵和基因组 DNA 方面具有天然活性。这些系统共同增加了 Cas9 靶向的可能性,并为天然宿主和异源基因组编辑提供了多路复用的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e842/6070500/e319cb21a55d/41598_2018_29746_Fig1_HTML.jpg

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