» Articles » PMID: 26929301

Friendly Fire: Biological Functions and Consequences of Chromosomal Targeting by CRISPR-Cas Systems

Overview
Journal J Bacteriol
Specialty Microbiology
Date 2016 Mar 2
PMID 26929301
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Clustered regularly interspaced short palindromic repeat (CRISPR)-associated (Cas) systems in bacteria and archaea target foreign elements, such as bacteriophages and conjugative plasmids, through the incorporation of short sequences (termed spacers) from the foreign element into the CRISPR array, thereby allowing sequence-specific targeting of the invader. Thus, CRISPR-Cas systems are typically considered a microbial adaptive immune system. While many of these incorporated spacers match targets on bacteriophages and plasmids, a noticeable number are derived from chromosomal DNA. While usually lethal to the self-targeting bacteria, in certain circumstances, these self-targeting spacers can have profound effects in regard to microbial biology, including functions beyond adaptive immunity. In this minireview, we discuss recent studies that focus on the functions and consequences of CRISPR-Cas self-targeting, including reshaping of the host population, group behavior modification, and the potential applications of CRISPR-Cas self-targeting as a tool in microbial biotechnology. Understanding the effects of CRISPR-Cas self-targeting is vital to fully understanding the spectrum of function of these systems.

Citing Articles

It's time to write a minireview.

OToole G J Bacteriol. 2024; 206(5):e0011324.

PMID: 38624220 PMC: 11112987. DOI: 10.1128/jb.00113-24.


Bacterial nucleoid is a riddle wrapped in a mystery inside an enigma.

Kuzminov A J Bacteriol. 2024; 206(3):e0021123.

PMID: 38358278 PMC: 10994824. DOI: 10.1128/jb.00211-23.


CRISPR-influenced symbiosis.

Reysenbach A, Terns M Nat Microbiol. 2023; 8(9):1611-1612.

PMID: 37580593 PMC: 10791070. DOI: 10.1038/s41564-023-01445-4.


A predicted CRISPR-mediated symbiosis between uncultivated archaea.

Esser S, Rahlff J, Zhao W, Predl M, Plewka J, Sures K Nat Microbiol. 2023; 8(9):1619-1633.

PMID: 37500801 DOI: 10.1038/s41564-023-01439-2.


crRNA complementarity shifts endogenous CRISPR-Cas systems between transcriptional repression and DNA defense.

Ratner H, Weiss D RNA Biol. 2021; 18(11):1560-1573.

PMID: 33733999 PMC: 8583161. DOI: 10.1080/15476286.2021.1878335.


References
1.
Jiang W, Samai P, Marraffini L . Degradation of Phage Transcripts by CRISPR-Associated RNases Enables Type III CRISPR-Cas Immunity. Cell. 2016; 164(4):710-21. PMC: 4752873. DOI: 10.1016/j.cell.2015.12.053. View

2.
Wiedenheft B, Lander G, Zhou K, Jore M, Brouns S, van der Oost J . Structures of the RNA-guided surveillance complex from a bacterial immune system. Nature. 2011; 477(7365):486-489. PMC: 4165517. DOI: 10.1038/nature10402. View

3.
Bikard D, Euler C, Jiang W, Nussenzweig P, Goldberg G, Duportet X . Exploiting CRISPR-Cas nucleases to produce sequence-specific antimicrobials. Nat Biotechnol. 2014; 32(11):1146-50. PMC: 4317352. DOI: 10.1038/nbt.3043. View

4.
Swarts D, Mosterd C, van Passel M, Brouns S . CRISPR interference directs strand specific spacer acquisition. PLoS One. 2012; 7(4):e35888. PMC: 3338789. DOI: 10.1371/journal.pone.0035888. View

5.
Terns R, Terns M . CRISPR-based technologies: prokaryotic defense weapons repurposed. Trends Genet. 2014; 30(3):111-8. PMC: 3981743. DOI: 10.1016/j.tig.2014.01.003. View