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A CRISPR toolbox to study virus–host interactions

Viruses depend on their hosts to complete their replication cycles; they exploit cellular receptors for entry and hijack cellular functions to replicate their genome, assemble progeny virions and spread. Recently, genome-scale CRISPR–Cas screens have been used to identify host factors that are requi...

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Detalles Bibliográficos
Autores principales: Puschnik, Andreas S., Majzoub, Karim, Ooi, Yaw Shin, Carette, Jan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800792/
https://www.ncbi.nlm.nih.gov/pubmed/28420884
http://dx.doi.org/10.1038/nrmicro.2017.29
Descripción
Sumario:Viruses depend on their hosts to complete their replication cycles; they exploit cellular receptors for entry and hijack cellular functions to replicate their genome, assemble progeny virions and spread. Recently, genome-scale CRISPR–Cas screens have been used to identify host factors that are required for virus replication, including the replication of clinically relevant viruses such as Zika virus, West Nile virus, dengue virus and hepatitis C virus. In this Review, we discuss the technical aspects of genome-scale knockout screens using CRISPR–Cas technology, and we compare these screens with alternative genetic screening technologies. The relative ease of use and reproducibility of CRISPR–Cas make it a powerful tool for probing virus–host interactions and for identifying new antiviral targets. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nrmicro.2017.29) contains supplementary material, which is available to authorized users.