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GenoMine:一种基于CRISPR-Cas9的用于生物遏制的杀灭开关 。 (注:原文句末不完整,翻译时根据已有内容尽量忠实翻译)

GenoMine: a CRISPR-Cas9-based kill switch for biocontainment of .

作者信息

Asin-Garcia Enrique, Martin-Pascual Maria, de Buck Claudia, Allewijn Max, Müller Alexandra, Martins Dos Santos Vitor A P

机构信息

Laboratory of Systems and Synthetic Biology, Wageningen University & Research, Wageningen, Netherlands.

Bioprocess Engineering Group, Wageningen University & Research, Wageningen, Netherlands.

出版信息

Front Bioeng Biotechnol. 2024 Sep 16;12:1426107. doi: 10.3389/fbioe.2024.1426107. eCollection 2024.

DOI:10.3389/fbioe.2024.1426107
PMID:39351062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11439788/
Abstract

Synthetic genetic circuits have revolutionised our capacity to control cell viability by conferring microorganisms with programmable functionalities to limit survival to specific environmental conditions. Here, we present the GenoMine safeguard, a CRISPR-Cas9-based kill switch for the biotechnological workhorse that employs repetitive genomic elements as cleavage targets to unleash a highly genotoxic response. To regulate the system's activation, we tested various circuit-based mechanisms including the digitalised version of an inducible expression system that operates at the transcriptional level and different options of post-transcriptional riboregulators. All of them were applied not only to directly control Cas9 and its lethal effects, but also to modulate the expression of two of its inhibitors: the AcrIIA4 anti-CRISPR protein and the transcriptional repressor TetR. Either upon direct induction of the endonuclease or under non-induced conditions of its inhibitors, the presence of Cas9 suppressed cell survival which could be exploited beyond biocontainment in situations where further CRISPR genome editing is undesirable.

摘要

合成基因电路通过赋予微生物可编程功能,使其仅在特定环境条件下存活,从而彻底改变了我们控制细胞活力的能力。在此,我们展示了GenoMine安全防护系统,这是一种基于CRISPR-Cas9的用于生物技术主力菌株的致死开关,它利用重复基因组元件作为切割靶点,引发高度基因毒性反应。为了调节系统的激活,我们测试了各种基于电路的机制,包括在转录水平运行的诱导表达系统的数字化版本以及转录后核糖调节因子的不同选项。所有这些机制不仅用于直接控制Cas9及其致死效应,还用于调节其两种抑制剂的表达:AcrIIA4抗CRISPR蛋白和转录阻遏物TetR。无论是在内切酶直接诱导后还是在其抑制剂的非诱导条件下,Cas9的存在都会抑制细胞存活,这在不希望进行进一步CRISPR基因组编辑的情况下,除了生物遏制之外还可加以利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/a0fcd9125cfc/fbioe-12-1426107-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/d059a6c51c76/fbioe-12-1426107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/60823014c570/fbioe-12-1426107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/76d431fafdad/fbioe-12-1426107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/f3603b885fb3/fbioe-12-1426107-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/a0fcd9125cfc/fbioe-12-1426107-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/d059a6c51c76/fbioe-12-1426107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/60823014c570/fbioe-12-1426107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/76d431fafdad/fbioe-12-1426107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/f3603b885fb3/fbioe-12-1426107-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11439788/a0fcd9125cfc/fbioe-12-1426107-g005.jpg

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Curr Opin Biotechnol. 2024 Feb;85:103025. doi: 10.1016/j.copbio.2023.103025. Epub 2023 Dec 7.
2
Exploring the Impact of Tensions in Stakeholder Norms on Designing for Value Change: The Case of Biosafety in Industrial Biotechnology.探讨利益相关者规范中的紧张关系对价值变革设计的影响:以工业生物技术中的生物安全为例。
Sci Eng Ethics. 2023 Mar 7;29(2):9. doi: 10.1007/s11948-023-00432-6.
3
Genetically stable CRISPR-based kill switches for engineered microbes.
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Synth Syst Biotechnol. 2024 Dec 20;10(2):356-364. doi: 10.1016/j.synbio.2024.12.005. eCollection 2025 Jun.
基于基因稳定的 CRISPR 工程菌杀伤开关
Nat Commun. 2022 Feb 3;13(1):672. doi: 10.1038/s41467-022-28163-5.
4
Streamlined CRISPR genome engineering in wild-type bacteria using SIBR-Cas.使用 SIBR-Cas 简化野生型细菌中的 CRISPR 基因组工程。
Nucleic Acids Res. 2021 Nov 8;49(19):11392-11404. doi: 10.1093/nar/gkab893.
5
ReScribe: An Unrestrained Tool Combining Multiplex Recombineering and Minimal-PAM ScCas9 for Genome Recoding .ReScribe:一种用于基因组重编码的无约束工具,结合了多重重组和最小化 PAM 的 SpCas9
ACS Synth Biol. 2021 Oct 15;10(10):2672-2688. doi: 10.1021/acssynbio.1c00297. Epub 2021 Sep 22.
6
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Nucleic Acids Res. 2021 Sep 20;49(16):9211-9228. doi: 10.1093/nar/gkab672.
7
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Curr Opin Biotechnol. 2021 Oct;71:25-31. doi: 10.1016/j.copbio.2021.05.004. Epub 2021 Jun 3.
8
A navigation guide of synthetic biology tools for Pseudomonas putida.用于恶臭假单胞菌的合成生物学工具导航指南。
Biotechnol Adv. 2021 Jul-Aug;49:107732. doi: 10.1016/j.biotechadv.2021.107732. Epub 2021 Mar 27.
9
Development of aptamer-based inhibitors for CRISPR/Cas system.基于适体的 CRISPR/Cas 系统抑制剂的开发。
Nucleic Acids Res. 2021 Feb 22;49(3):1330-1344. doi: 10.1093/nar/gkaa865.
10
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N Biotechnol. 2021 Jan 25;60:44-51. doi: 10.1016/j.nbt.2020.08.004. Epub 2020 Sep 2.