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CRISPR–Cas9 Genetic Analysis of Virus–Host Interactions
Clustered regularly interspaced short palindromic repeats (CRISPR) has greatly expanded the ability to genetically probe virus–host interactions. CRISPR systems enable focused or systematic, genomewide studies of nearly all aspects of a virus lifecycle. Combined with its relative ease of use and hig...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850362/ https://www.ncbi.nlm.nih.gov/pubmed/29385696 http://dx.doi.org/10.3390/v10020055 |
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author | Gebre, Makda Nomburg, Jason L. Gewurz, Benjamin E. |
author_facet | Gebre, Makda Nomburg, Jason L. Gewurz, Benjamin E. |
author_sort | Gebre, Makda |
collection | PubMed |
description | Clustered regularly interspaced short palindromic repeats (CRISPR) has greatly expanded the ability to genetically probe virus–host interactions. CRISPR systems enable focused or systematic, genomewide studies of nearly all aspects of a virus lifecycle. Combined with its relative ease of use and high reproducibility, CRISPR is becoming an essential tool in studies of the host factors important for viral pathogenesis. Here, we review the use of CRISPR–Cas9 for the loss-of-function analysis of host dependency factors. We focus on the use of CRISPR-pooled screens for the systematic identification of host dependency factors, particularly in Epstein–Barr virus-transformed B cells. We also discuss the use of CRISPR interference (CRISPRi) and gain-of-function CRISPR activation (CRISPRa) approaches to probe virus–host interactions. Finally, we comment on the future directions enabled by combinatorial CRISPR screens. |
format | Online Article Text |
id | pubmed-5850362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58503622018-03-16 CRISPR–Cas9 Genetic Analysis of Virus–Host Interactions Gebre, Makda Nomburg, Jason L. Gewurz, Benjamin E. Viruses Review Clustered regularly interspaced short palindromic repeats (CRISPR) has greatly expanded the ability to genetically probe virus–host interactions. CRISPR systems enable focused or systematic, genomewide studies of nearly all aspects of a virus lifecycle. Combined with its relative ease of use and high reproducibility, CRISPR is becoming an essential tool in studies of the host factors important for viral pathogenesis. Here, we review the use of CRISPR–Cas9 for the loss-of-function analysis of host dependency factors. We focus on the use of CRISPR-pooled screens for the systematic identification of host dependency factors, particularly in Epstein–Barr virus-transformed B cells. We also discuss the use of CRISPR interference (CRISPRi) and gain-of-function CRISPR activation (CRISPRa) approaches to probe virus–host interactions. Finally, we comment on the future directions enabled by combinatorial CRISPR screens. MDPI 2018-01-30 /pmc/articles/PMC5850362/ /pubmed/29385696 http://dx.doi.org/10.3390/v10020055 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Gebre, Makda Nomburg, Jason L. Gewurz, Benjamin E. CRISPR–Cas9 Genetic Analysis of Virus–Host Interactions |
title | CRISPR–Cas9 Genetic Analysis of Virus–Host Interactions |
title_full | CRISPR–Cas9 Genetic Analysis of Virus–Host Interactions |
title_fullStr | CRISPR–Cas9 Genetic Analysis of Virus–Host Interactions |
title_full_unstemmed | CRISPR–Cas9 Genetic Analysis of Virus–Host Interactions |
title_short | CRISPR–Cas9 Genetic Analysis of Virus–Host Interactions |
title_sort | crispr–cas9 genetic analysis of virus–host interactions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850362/ https://www.ncbi.nlm.nih.gov/pubmed/29385696 http://dx.doi.org/10.3390/v10020055 |
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