Literature DB >> 21294681

Clustered regularly interspaced short palindromic repeats (CRISPRs): the hallmark of an ingenious antiviral defense mechanism in prokaryotes.

Sinan Al-Attar1, Edze R Westra, John van der Oost, Stan J J Brouns.   

Abstract

Many prokaryotes contain the recently discovered defense system against mobile genetic elements. This defense system contains a unique type of repetitive DNA stretches, termed Clustered Regularly Interspaced Short Palindromic Repeats (CRISPRs). CRISPRs consist of identical repeated DNA sequences (repeats), interspaced by highly variable sequences referred to as spacers. The spacers originate from either phages or plasmids and comprise the prokaryotes' 'immunological memory'. CRISPR-associated (cas) genes encode conserved proteins that together with CRISPRs make-up the CRISPR/Cas system, responsible for defending the prokaryotic cell against invaders. CRISPR-mediated resistance has been proposed to involve three stages: (i) CRISPR-Adaptation, the invader DNA is encountered by the CRISPR/Cas machinery and an invader-derived short DNA fragment is incorporated in the CRISPR array. (ii) CRISPR-Expression, the CRISPR array is transcribed and the transcript is processed by Cas proteins. (iii) CRISPR-Interference, the invaders' nucleic acid is recognized by complementarity to the crRNA and neutralized. An application of the CRISPR/Cas system is the immunization of industry-relevant prokaryotes (or eukaryotes) against mobile-genetic invasion. In addition, the high variability of the CRISPR spacer content can be exploited for phylogenetic and evolutionary studies. Despite impressive progress during the last couple of years, the elucidation of several fundamental details will be a major challenge in future research.

Entities:  

Mesh:

Year:  2011        PMID: 21294681     DOI: 10.1515/BC.2011.042

Source DB:  PubMed          Journal:  Biol Chem        ISSN: 1431-6730            Impact factor:   3.915


  81 in total

1.  Nature and intensity of selection pressure on CRISPR-associated genes.

Authors:  Nobuto Takeuchi; Yuri I Wolf; Kira S Makarova; Eugene V Koonin
Journal:  J Bacteriol       Date:  2011-12-16       Impact factor: 3.490

2.  Facilitation of CRISPR adaptation.

Authors:  Stephen T Abedon
Journal:  Bacteriophage       Date:  2011-05-01

3.  Mechanism of substrate selection by a highly specific CRISPR endoribonuclease.

Authors:  Samuel H Sternberg; Rachel E Haurwitz; Jennifer A Doudna
Journal:  RNA       Date:  2012-02-16       Impact factor: 4.942

Review 4.  RNA-guided genetic silencing systems in bacteria and archaea.

Authors:  Blake Wiedenheft; Samuel H Sternberg; Jennifer A Doudna
Journal:  Nature       Date:  2012-02-15       Impact factor: 49.962

5.  Association of clustered regularly interspaced short palindromic repeat (CRISPR) elements with specific serotypes and virulence potential of shiga toxin-producing Escherichia coli.

Authors:  Magaly Toro; Guojie Cao; Wenting Ju; Marc Allard; Rodolphe Barrangou; Shaohua Zhao; Eric Brown; Jianghong Meng
Journal:  Appl Environ Microbiol       Date:  2013-12-13       Impact factor: 4.792

6.  DMS3-42: the secret to CRISPR-dependent biofilm inhibition in Pseudomonas aeruginosa.

Authors:  Kelli L Palmer; Marvin Whiteley
Journal:  J Bacteriol       Date:  2011-05-06       Impact factor: 3.490

7.  Genome-wide correlation analysis suggests different roles of CRISPR-Cas systems in the acquisition of antibiotic resistance genes in diverse species.

Authors:  Saadlee Shehreen; Te-Yuan Chyou; Peter C Fineran; Chris M Brown
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2019-05-13       Impact factor: 6.237

Review 8.  Suppressing the CRISPR/Cas adaptive immune system in bacterial infections.

Authors:  P Gholizadeh; M Aghazadeh; M Asgharzadeh; H S Kafil
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2017-06-11       Impact factor: 3.267

9.  Adaptation and modification of three CRISPR loci in two closely related cyanobacteria.

Authors:  Stephanie Hein; Ingeborg Scholz; Björn Voß; Wolfgang R Hess
Journal:  RNA Biol       Date:  2013-03-27       Impact factor: 4.652

10.  Two CRISPR-Cas systems in Methanosarcina mazei strain Gö1 display common processing features despite belonging to different types I and III.

Authors:  Lisa Nickel; Katrin Weidenbach; Dominik Jäger; Rolf Backofen; Sita J Lange; Nadja Heidrich; Ruth A Schmitz
Journal:  RNA Biol       Date:  2013-04-25       Impact factor: 4.652

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.