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Genome-wide activation screens to increase adeno-associated virus production
We describe a genome-wide screening strategy to identify target genes whose modulation increases the capacity of a cell to produce recombinant adeno-associated viral (AAV) vector. Specifically, a single-guide RNA (sgRNA) library for a CRISPR-based genome-wide transcriptional activation screen was in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413672/ https://www.ncbi.nlm.nih.gov/pubmed/34513296 http://dx.doi.org/10.1016/j.omtn.2021.06.026 |
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author | Barnes, Christopher R. Lee, Hyuncheol Ojala, David S. Lewis, Kazuomori K. Limsirichai, Prajit Schaffer, David V. |
author_facet | Barnes, Christopher R. Lee, Hyuncheol Ojala, David S. Lewis, Kazuomori K. Limsirichai, Prajit Schaffer, David V. |
author_sort | Barnes, Christopher R. |
collection | PubMed |
description | We describe a genome-wide screening strategy to identify target genes whose modulation increases the capacity of a cell to produce recombinant adeno-associated viral (AAV) vector. Specifically, a single-guide RNA (sgRNA) library for a CRISPR-based genome-wide transcriptional activation screen was inserted into an AAV vector, and iterative rounds of viral infection and rescue in HEK293 producer cells enabled the enrichment of sgRNAs targeting genes whose upregulation increased AAV production. Numerous gain-of-function targets were identified, including spindle and kinetochore associated complex subunit 2 (SKA2) and inositol 1, 4, 5-trisphosphate receptor interacting protein (ITPRIP). Furthermore, individual or combinatorial modulation of these targets in stable producer cell lines increased vector genomic replication and loading into AAV virions, resulting in up to a 3.8-fold increase in AAV manufacturing capacity. Our study offers an efficient approach to engineer viral vector producer cell lines and enhances our understanding of the roles of SKA2 and ITPRIP in AAV packaging. |
format | Online Article Text |
id | pubmed-8413672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-84136722021-09-10 Genome-wide activation screens to increase adeno-associated virus production Barnes, Christopher R. Lee, Hyuncheol Ojala, David S. Lewis, Kazuomori K. Limsirichai, Prajit Schaffer, David V. Mol Ther Nucleic Acids Original Article We describe a genome-wide screening strategy to identify target genes whose modulation increases the capacity of a cell to produce recombinant adeno-associated viral (AAV) vector. Specifically, a single-guide RNA (sgRNA) library for a CRISPR-based genome-wide transcriptional activation screen was inserted into an AAV vector, and iterative rounds of viral infection and rescue in HEK293 producer cells enabled the enrichment of sgRNAs targeting genes whose upregulation increased AAV production. Numerous gain-of-function targets were identified, including spindle and kinetochore associated complex subunit 2 (SKA2) and inositol 1, 4, 5-trisphosphate receptor interacting protein (ITPRIP). Furthermore, individual or combinatorial modulation of these targets in stable producer cell lines increased vector genomic replication and loading into AAV virions, resulting in up to a 3.8-fold increase in AAV manufacturing capacity. Our study offers an efficient approach to engineer viral vector producer cell lines and enhances our understanding of the roles of SKA2 and ITPRIP in AAV packaging. American Society of Gene & Cell Therapy 2021-07-16 /pmc/articles/PMC8413672/ /pubmed/34513296 http://dx.doi.org/10.1016/j.omtn.2021.06.026 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Barnes, Christopher R. Lee, Hyuncheol Ojala, David S. Lewis, Kazuomori K. Limsirichai, Prajit Schaffer, David V. Genome-wide activation screens to increase adeno-associated virus production |
title | Genome-wide activation screens to increase adeno-associated virus production |
title_full | Genome-wide activation screens to increase adeno-associated virus production |
title_fullStr | Genome-wide activation screens to increase adeno-associated virus production |
title_full_unstemmed | Genome-wide activation screens to increase adeno-associated virus production |
title_short | Genome-wide activation screens to increase adeno-associated virus production |
title_sort | genome-wide activation screens to increase adeno-associated virus production |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413672/ https://www.ncbi.nlm.nih.gov/pubmed/34513296 http://dx.doi.org/10.1016/j.omtn.2021.06.026 |
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