Keeping crispr in check

diverse mechanisms of phage-encoded anti-crisprs

Review (2019)
Author(s)

Despoina Trasanidou (Wageningen University & Research)

Ana Sousa Gerós (Kavli institute of nanoscience Delft)

Prarthana Mohanraju (Wageningen University & Research)

Anna Cornelia Nieuwenweg (Wageningen University & Research)

Franklin L. Luzia de Nobrega (Kavli institute of nanoscience Delft, TU Delft - BN/Stan Brouns Lab)

Raymond H.J. H.J. Staals (Wageningen University & Research)

Research Group
BN/Stan Brouns Lab
Copyright
© 2019 Despoina Trasanidou, Ana Sousa Gerós, Prarthana Mohanraju, Anna Cornelia Nieuwenweg, F. Luzia de Nobrega, Raymond H.J. Staals
DOI related publication
https://doi.org/10.1093/femsle/fnz098
More Info
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Publication Year
2019
Language
English
Copyright
© 2019 Despoina Trasanidou, Ana Sousa Gerós, Prarthana Mohanraju, Anna Cornelia Nieuwenweg, F. Luzia de Nobrega, Raymond H.J. Staals
Research Group
BN/Stan Brouns Lab
Issue number
9
Volume number
366
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Abstract

CRISPR-Cas represents the only adaptive immune system of prokaryotes known to date. These immune systems are widespread among bacteria and archaea, and provide protection against invasion of mobile genetic elements, such as bacteriophages and plasmids. As a result of the arms-race between phages and their prokaryotic hosts, phages have evolved inhibitors known as anti-CRISPR (Acr) proteins to evade CRISPR immunity. In the recent years, several Acr proteins have been described in both temperate and virulent phages targeting diverse CRISPR-Cas systems. Here, we describe the strategies of Acr discovery and the multiple molecular mechanisms by which these proteins operate to inhibit CRISPR immunity. We discuss the biological relevance of Acr proteins and speculate on the implications of their activity for the development of improved CRISPR-based research and biotechnological tools.