Literature DB >> 32238445

CRISPR Tools To Control Gene Expression in Bacteria.

Antoine Vigouroux1,2, David Bikard3.   

Abstract

CRISPR-Cas systems have been engineered as powerful tools to control gene expression in bacteria. The most common strategy relies on the use of Cas effectors modified to bind target DNA without introducing DNA breaks. These effectors can either block the RNA polymerase or recruit it through activation domains. Here, we discuss the mechanistic details of how Cas effectors can modulate gene expression by blocking transcription initiation or acting as transcription roadblocks. CRISPR-Cas tools can be further engineered to obtain fine-tuned control of gene expression or target multiple genes simultaneously. Several caveats in using these tools have also been revealed, including off-target effects and toxicity, making it important to understand the design rules of engineered CRISPR-Cas effectors in bacteria. Alternatively, some types of CRISPR-Cas systems target RNA and could be used to block gene expression at the posttranscriptional level. Finally, we review applications of these tools in high-throughput screens and the progress and challenges in introducing CRISPR knockdown to other species, including nonmodel bacteria with industrial or clinical relevance. A deep understanding of how CRISPR-Cas systems can be harnessed to control gene expression in bacteria and build powerful tools will certainly open novel research directions.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  CRISPR; gene silencing; transcriptional regulation

Mesh:

Year:  2020        PMID: 32238445      PMCID: PMC7117552          DOI: 10.1128/MMBR.00077-19

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  135 in total

1.  Identification of critical staphylococcal genes using conditional phenotypes generated by antisense RNA.

Authors:  Y Ji; B Zhang; S F Van; P Warren; G Woodnutt; M K Burnham; M Rosenberg
Journal:  Science       Date:  2001-09-21       Impact factor: 47.728

Review 2.  New aspects of RNA processing in prokaryotes.

Authors:  Elena Evguenieva-Hackenberg; Gabriele Klug
Journal:  Curr Opin Microbiol       Date:  2011-09-22       Impact factor: 7.934

Review 3.  A brief history of RNAi: the silence of the genes.

Authors:  George L Sen; Helen M Blau
Journal:  FASEB J       Date:  2006-07       Impact factor: 5.191

4.  Systematic analysis of CRISPR-Cas9 mismatch tolerance reveals low levels of off-target activity.

Authors:  Emily M Anderson; Amanda Haupt; John A Schiel; Eldon Chou; Hidevaldo B Machado; Žaklina Strezoska; Steve Lenger; Shawn McClelland; Amanda Birmingham; Annaleen Vermeulen; Anja van Brabant Smith
Journal:  J Biotechnol       Date:  2015-07-17       Impact factor: 3.307

5.  A cyclic oligonucleotide signaling pathway in type III CRISPR-Cas systems.

Authors:  Migle Kazlauskiene; Georgij Kostiuk; Česlovas Venclovas; Gintautas Tamulaitis; Virginijus Siksnys
Journal:  Science       Date:  2017-06-29       Impact factor: 47.728

6.  Repurposing endogenous type I CRISPR-Cas systems for programmable gene repression.

Authors:  Michelle L Luo; Adam S Mullis; Ryan T Leenay; Chase L Beisel
Journal:  Nucleic Acids Res       Date:  2014-10-17       Impact factor: 16.971

7.  Author Correction: Synthetic CRISPR-Cas gene activators for transcriptional reprogramming in bacteria.

Authors:  Chen Dong; Jason Fontana; Anika Patel; James M Carothers; Jesse G Zalatan
Journal:  Nat Commun       Date:  2018-10-15       Impact factor: 14.919

8.  Bacillus subtilis cell diameter is determined by the opposing actions of two distinct cell wall synthetic systems.

Authors:  Michael F Dion; Mrinal Kapoor; Yingjie Sun; Sean Wilson; Joel Ryan; Antoine Vigouroux; Sven van Teeffelen; Rudolf Oldenbourg; Ethan C Garner
Journal:  Nat Microbiol       Date:  2019-05-13       Impact factor: 17.745

9.  Programmable CRISPR-Cas transcriptional activation in bacteria.

Authors:  Hsing-I Ho; Jennifer R Fang; Jacky Cheung; Harris H Wang
Journal:  Mol Syst Biol       Date:  2020-07       Impact factor: 11.429

10.  Synthetic circuits reveal how mechanisms of gene regulatory networks constrain evolution.

Authors:  Yolanda Schaerli; Alba Jiménez; José M Duarte; Ljiljana Mihajlovic; Julien Renggli; Mark Isalan; James Sharpe; Andreas Wagner
Journal:  Mol Syst Biol       Date:  2018-09-10       Impact factor: 11.429

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  15 in total

Review 1.  Cross-species RNA-seq for deciphering host-microbe interactions.

Authors:  Alexander J Westermann; Jörg Vogel
Journal:  Nat Rev Genet       Date:  2021-02-17       Impact factor: 53.242

Review 2.  Bacterial CRISPR screens for gene function.

Authors:  Horia Todor; Melanie R Silvis; Hendrik Osadnik; Carol A Gross
Journal:  Curr Opin Microbiol       Date:  2020-12-04       Impact factor: 7.934

3.  The impact of genetic diversity on gene essentiality within the Escherichia coli species.

Authors:  François Rousset; Jose Cabezas-Caballero; Florence Piastra-Facon; Jesús Fernández-Rodríguez; Olivier Clermont; Erick Denamur; Eduardo P C Rocha; David Bikard
Journal:  Nat Microbiol       Date:  2021-01-18       Impact factor: 17.745

4.  Synthetic fused sRNA for the simultaneous repression of multiple genes.

Authors:  Jinho Yeom; Jong Seong Park; Yong Min Jeon; Beom Seop Song; Seung Min Yoo
Journal:  Appl Microbiol Biotechnol       Date:  2022-03-15       Impact factor: 4.813

Review 5.  CRISPRi-seq for genome-wide fitness quantification in bacteria.

Authors:  Vincent de Bakker; Xue Liu; Afonso M Bravo; Jan-Willem Veening
Journal:  Nat Protoc       Date:  2022-01-07       Impact factor: 17.021

6.  Computational pipeline for designing guide RNAs for mismatch-CRISPRi.

Authors:  Jordi van Gestel; John S Hawkins; Horia Todor; Carol A Gross
Journal:  STAR Protoc       Date:  2021-05-05

Review 7.  CRISPR technologies and the search for the PAM-free nuclease.

Authors:  Daphne Collias; Chase L Beisel
Journal:  Nat Commun       Date:  2021-01-22       Impact factor: 14.919

8.  Programmable Gene Knockdown in Diverse Bacteria Using Mobile-CRISPRi.

Authors:  Amy B Banta; Ryan D Ward; Jennifer S Tran; Emily E Bacon; Jason M Peters
Journal:  Curr Protoc Microbiol       Date:  2020-12

9.  A High-Efficacy CRISPR Interference System for Gene Function Discovery in Zymomonas mobilis.

Authors:  Amy B Banta; Amy L Enright; Cheta Siletti; Jason M Peters
Journal:  Appl Environ Microbiol       Date:  2020-11-10       Impact factor: 4.792

Review 10.  CRISPR-based gene expression control for synthetic gene circuits.

Authors:  Javier Santos-Moreno; Yolanda Schaerli
Journal:  Biochem Soc Trans       Date:  2020-10-30       Impact factor: 5.407

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