A CRISPR-Based Screen Identifies Genes Essential for West-Nile-Virus-Induced Cell Death

West Nile virus (WNV) causes an acute neurological infection attended by massive neuronal cell death. However, the mechanism(s) behind the virus-induced cell death is poorly understood. Using a library containing 77,406 sgRNAs targeting 20,121 genes, we performed a genome-wide screen followed by a s...

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Main Authors: Hongming Ma, Ying Dang, Yonggan Wu, Gengxiang Jia, Edgar Anaya, Junli Zhang, Sojan Abraham, Jang-Gi Choi, Guojun Shi, Ling Qi, N. Manjunath, Haoquan Wu
Format: Article
Language:English
Published: Elsevier 2015-07-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124715006750
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spelling doaj-db801ee050da440190b4ff28a57f02c82020-11-24T22:11:21ZengElsevierCell Reports2211-12472015-07-0112467368310.1016/j.celrep.2015.06.049A CRISPR-Based Screen Identifies Genes Essential for West-Nile-Virus-Induced Cell DeathHongming Ma0Ying Dang1Yonggan Wu2Gengxiang Jia3Edgar Anaya4Junli Zhang5Sojan Abraham6Jang-Gi Choi7Guojun Shi8Ling Qi9N. Manjunath10Haoquan Wu11Center of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USACenter of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USALabii LLC, Mountain View, CA 94043, USACenter of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USACenter of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USACenter of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USACenter of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USACenter of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USADivision of Nutritional Sciences, Cornell University, Ithaca, NY 14853, USADivision of Nutritional Sciences, Cornell University, Ithaca, NY 14853, USACenter of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USACenter of Emphasis in Infectious Diseases, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USAWest Nile virus (WNV) causes an acute neurological infection attended by massive neuronal cell death. However, the mechanism(s) behind the virus-induced cell death is poorly understood. Using a library containing 77,406 sgRNAs targeting 20,121 genes, we performed a genome-wide screen followed by a second screen with a sub-library. Among the genes identified, seven genes, EMC2, EMC3, SEL1L, DERL2, UBE2G2, UBE2J1, and HRD1, stood out as having the strongest phenotype, whose knockout conferred strong protection against WNV-induced cell death with two different WNV strains and in three cell lines. Interestingly, knockout of these genes did not block WNV replication. Thus, these appear to be essential genes that link WNV replication to downstream cell death pathway(s). In addition, the fact that all of these genes belong to the ER-associated protein degradation (ERAD) pathway suggests that this might be the primary driver of WNV-induced cell death.http://www.sciencedirect.com/science/article/pii/S2211124715006750
collection DOAJ
language English
format Article
sources DOAJ
author Hongming Ma
Ying Dang
Yonggan Wu
Gengxiang Jia
Edgar Anaya
Junli Zhang
Sojan Abraham
Jang-Gi Choi
Guojun Shi
Ling Qi
N. Manjunath
Haoquan Wu
spellingShingle Hongming Ma
Ying Dang
Yonggan Wu
Gengxiang Jia
Edgar Anaya
Junli Zhang
Sojan Abraham
Jang-Gi Choi
Guojun Shi
Ling Qi
N. Manjunath
Haoquan Wu
A CRISPR-Based Screen Identifies Genes Essential for West-Nile-Virus-Induced Cell Death
Cell Reports
author_facet Hongming Ma
Ying Dang
Yonggan Wu
Gengxiang Jia
Edgar Anaya
Junli Zhang
Sojan Abraham
Jang-Gi Choi
Guojun Shi
Ling Qi
N. Manjunath
Haoquan Wu
author_sort Hongming Ma
title A CRISPR-Based Screen Identifies Genes Essential for West-Nile-Virus-Induced Cell Death
title_short A CRISPR-Based Screen Identifies Genes Essential for West-Nile-Virus-Induced Cell Death
title_full A CRISPR-Based Screen Identifies Genes Essential for West-Nile-Virus-Induced Cell Death
title_fullStr A CRISPR-Based Screen Identifies Genes Essential for West-Nile-Virus-Induced Cell Death
title_full_unstemmed A CRISPR-Based Screen Identifies Genes Essential for West-Nile-Virus-Induced Cell Death
title_sort crispr-based screen identifies genes essential for west-nile-virus-induced cell death
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2015-07-01
description West Nile virus (WNV) causes an acute neurological infection attended by massive neuronal cell death. However, the mechanism(s) behind the virus-induced cell death is poorly understood. Using a library containing 77,406 sgRNAs targeting 20,121 genes, we performed a genome-wide screen followed by a second screen with a sub-library. Among the genes identified, seven genes, EMC2, EMC3, SEL1L, DERL2, UBE2G2, UBE2J1, and HRD1, stood out as having the strongest phenotype, whose knockout conferred strong protection against WNV-induced cell death with two different WNV strains and in three cell lines. Interestingly, knockout of these genes did not block WNV replication. Thus, these appear to be essential genes that link WNV replication to downstream cell death pathway(s). In addition, the fact that all of these genes belong to the ER-associated protein degradation (ERAD) pathway suggests that this might be the primary driver of WNV-induced cell death.
url http://www.sciencedirect.com/science/article/pii/S2211124715006750
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