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mSystems. 2024 Jan 23;9(1):e0081523. doi: 10.1128/msystems.00815-23. Epub 2023 Dec 21.
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Essential gene knockdowns reveal genetic vulnerabilities and antibiotic sensitivities in .必需基因敲低揭示了. 的遗传脆弱性和抗生素敏感性。
mBio. 2024 Feb 14;15(2):e0205123. doi: 10.1128/mbio.02051-23. Epub 2023 Dec 21.
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The genetics of aerotolerant growth in an alphaproteobacterium with a naturally reduced genome.具有自然简化基因组的α变形菌的耐氧生长的遗传学。
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Flux-Balance Analysis and Mobile CRISPRi-Guided Deletion of a Conditionally Essential Gene in MR-1.通量平衡分析和移动 CRISPRi 引导的条件必需基因在 MR-1 中的缺失
ACS Synth Biol. 2022 Oct 21;11(10):3405-3413. doi: 10.1021/acssynbio.2c00323. Epub 2022 Oct 11.
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Cargo Genes of Tn-Like Transposons Comprise an Enormous Diversity of Defense Systems, Mobile Genetic Elements, and Antibiotic Resistance Genes.Tn 样转座子的基因包含了大量的防御系统、可移动遗传因子和抗生素抗性基因。
mBio. 2021 Dec 21;12(6):e0293821. doi: 10.1128/mBio.02938-21. Epub 2021 Dec 7.
7
The quorum-sensing systems of Vibrio campbellii DS40M4 and BB120 are genetically and functionally distinct.坎贝尔氏弧菌 DS40M4 和 BB120 的群体感应系统在遗传和功能上是不同的。
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8
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9
Dual-function quorum-sensing systems in bacterial pathogens and symbionts.细菌病原体和共生体中的双功能群体感应系统。
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10
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Appl Environ Microbiol. 2020 Nov 10;86(23). doi: 10.1128/AEM.01621-20.

利用移动 CRISPRi 作为调控基因表达的强大工具

Mobile-CRISPRi as a powerful tool for modulating gene expression.

机构信息

Department of Biology, Indiana University, Bloomington, Indiana, USA.

Department of Microbiology, School of Medicine, University of Washington, Seattle, Washington, USA.

出版信息

Appl Environ Microbiol. 2024 Jun 18;90(6):e0006524. doi: 10.1128/aem.00065-24. Epub 2024 May 22.

DOI:10.1128/aem.00065-24
PMID:38775491
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11218623/
Abstract

CRISPRi (Clustered Regularly Interspaced Palindromic Repeats interference) is a gene knockdown method that uses a deactivated Cas9 protein (dCas9) that binds a specific gene target locus dictated by an encoded guide RNA (sgRNA) to block transcription. Mobile-CRISPRi is a suite of modular vectors that enable CRISPRi knockdowns in diverse bacteria by integrating IPTG-inducible and genes into the genome using Tn transposition. Here, we show that the Mobile-CRISPRi system functions robustly and specifically in multiple species: , , , , and . We demonstrate efficacy by targeting both essential and non-essential genes that function to produce defined, measurable phenotypes: bioluminescence, quorum sensing, cell division, and growth arrest. We anticipate that Mobile-CRISPRi will be used in species to systematically probe gene function and essentiality in various behaviors and native environments.IMPORTANCEThe genetic manipulation of bacterial genomes is an invaluable tool in experimental microbiology. The development of CRISPRi (Clustered Regularly Interspaced Palindromic Repeats interference) tools has revolutionized genetics in many organisms, including bacteria. Here, we optimized the use of Mobile-CRISPRi in five species, each of which has significant impacts on marine environments and organisms that include squid, shrimp, shellfish, finfish, corals, and multiple of which pose direct threats to human health. The Mobile-CRISPRi technology is easily adaptable, moveable from strain to strain, and enables researchers to selectively turn off gene expression. Our experiments demonstrate Mobile-CRISPRi is effective and robust at repressing gene expression of both essential and non-essential genes in species.

摘要

CRISPRi(成簇规律间隔短回文重复干扰)是一种基因敲低方法,它使用一种失活的 Cas9 蛋白(dCas9),该蛋白结合由编码向导 RNA(sgRNA)指定的特定基因靶标位点,从而阻断转录。Mobile-CRISPRi 是一套模块化载体,通过使用 Tn 转座将 IPTG 诱导的基因和基因整合到基因组中,从而在多种细菌中实现 CRISPRi 敲低。在这里,我们表明 Mobile-CRISPRi 系统在多个物种中都能稳健且特异性地发挥作用:、、、、和。我们通过靶向既为产生明确、可测量的表型(生物发光、群体感应、细胞分裂和生长停滞)又发挥作用的必需和非必需基因来证明其功效。我们预计 Mobile-CRISPRi 将在 物种中用于系统地研究各种行为和自然环境中基因的功能和必需性。

重要性

细菌基因组的遗传操作是实验微生物学中非常有价值的工具。CRISPRi(成簇规律间隔短回文重复干扰)工具的发展彻底改变了许多生物体(包括细菌)的遗传学。在这里,我们优化了 Mobile-CRISPRi 在五个物种中的使用,每个物种都对海洋环境和包括鱿鱼、虾、贝类、鱼类、珊瑚在内的生物体有重大影响,其中许多对人类健康构成直接威胁。Mobile-CRISPRi 技术易于适应,可在菌株之间移动,并使研究人员能够选择性地关闭基因表达。我们的实验表明,Mobile-CRISPRi 在物种中有效地抑制必需和非必需基因的基因表达是稳健的。