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A versatile viral toolkit for functional discovery in the nervous system
The ability to precisely control transgene expression is essential for basic research and clinical applications. Adeno-associated viruses (AAVs) are non-pathogenic and can be used to drive stable expression in virtually any tissue, cell type, or species, but their limited genomic payload results in...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243523/ https://www.ncbi.nlm.nih.gov/pubmed/35784651 http://dx.doi.org/10.1016/j.crmeth.2022.100225 |
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author | Pouchelon, Gabrielle Vergara, Josselyn McMahon, Justin Gorissen, Bram L. Lin, Jessica D. Vormstein-Schneider, Douglas Niehaus, Jason L. Burbridge, Timothy J. Wester, Jason C. Sherer, Mia Fernandez-Otero, Marian Allaway, Kathryn C. Pelkey, Kenneth Chittajallu, Ramesh McBain, Chris J. Fan, Melina Nasse, Jason S. Wildenberg, Gregg A. Fishell, Gordon Dimidschstein, Jordane |
author_facet | Pouchelon, Gabrielle Vergara, Josselyn McMahon, Justin Gorissen, Bram L. Lin, Jessica D. Vormstein-Schneider, Douglas Niehaus, Jason L. Burbridge, Timothy J. Wester, Jason C. Sherer, Mia Fernandez-Otero, Marian Allaway, Kathryn C. Pelkey, Kenneth Chittajallu, Ramesh McBain, Chris J. Fan, Melina Nasse, Jason S. Wildenberg, Gregg A. Fishell, Gordon Dimidschstein, Jordane |
author_sort | Pouchelon, Gabrielle |
collection | PubMed |
description | The ability to precisely control transgene expression is essential for basic research and clinical applications. Adeno-associated viruses (AAVs) are non-pathogenic and can be used to drive stable expression in virtually any tissue, cell type, or species, but their limited genomic payload results in a trade-off between the transgenes that can be incorporated and the complexity of the regulatory elements controlling their expression. Resolving these competing imperatives in complex experiments inevitably results in compromises. Here, we assemble an optimized viral toolkit (VTK) that addresses these limitations and allows for efficient combinatorial targeting of cell types. Moreover, their modular design explicitly enables further refinements. We achieve this in compact vectors by integrating structural improvements of AAV vectors with innovative molecular tools. We illustrate the potential of this approach through a systematic demonstration of their utility for targeting cell types and querying their biology using a wide array of genetically encoded tools. |
format | Online Article Text |
id | pubmed-9243523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92435232022-07-01 A versatile viral toolkit for functional discovery in the nervous system Pouchelon, Gabrielle Vergara, Josselyn McMahon, Justin Gorissen, Bram L. Lin, Jessica D. Vormstein-Schneider, Douglas Niehaus, Jason L. Burbridge, Timothy J. Wester, Jason C. Sherer, Mia Fernandez-Otero, Marian Allaway, Kathryn C. Pelkey, Kenneth Chittajallu, Ramesh McBain, Chris J. Fan, Melina Nasse, Jason S. Wildenberg, Gregg A. Fishell, Gordon Dimidschstein, Jordane Cell Rep Methods Report The ability to precisely control transgene expression is essential for basic research and clinical applications. Adeno-associated viruses (AAVs) are non-pathogenic and can be used to drive stable expression in virtually any tissue, cell type, or species, but their limited genomic payload results in a trade-off between the transgenes that can be incorporated and the complexity of the regulatory elements controlling their expression. Resolving these competing imperatives in complex experiments inevitably results in compromises. Here, we assemble an optimized viral toolkit (VTK) that addresses these limitations and allows for efficient combinatorial targeting of cell types. Moreover, their modular design explicitly enables further refinements. We achieve this in compact vectors by integrating structural improvements of AAV vectors with innovative molecular tools. We illustrate the potential of this approach through a systematic demonstration of their utility for targeting cell types and querying their biology using a wide array of genetically encoded tools. Elsevier 2022-05-26 /pmc/articles/PMC9243523/ /pubmed/35784651 http://dx.doi.org/10.1016/j.crmeth.2022.100225 Text en © 2022 The Author(s) 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 | Report Pouchelon, Gabrielle Vergara, Josselyn McMahon, Justin Gorissen, Bram L. Lin, Jessica D. Vormstein-Schneider, Douglas Niehaus, Jason L. Burbridge, Timothy J. Wester, Jason C. Sherer, Mia Fernandez-Otero, Marian Allaway, Kathryn C. Pelkey, Kenneth Chittajallu, Ramesh McBain, Chris J. Fan, Melina Nasse, Jason S. Wildenberg, Gregg A. Fishell, Gordon Dimidschstein, Jordane A versatile viral toolkit for functional discovery in the nervous system |
title | A versatile viral toolkit for functional discovery in the nervous system |
title_full | A versatile viral toolkit for functional discovery in the nervous system |
title_fullStr | A versatile viral toolkit for functional discovery in the nervous system |
title_full_unstemmed | A versatile viral toolkit for functional discovery in the nervous system |
title_short | A versatile viral toolkit for functional discovery in the nervous system |
title_sort | versatile viral toolkit for functional discovery in the nervous system |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243523/ https://www.ncbi.nlm.nih.gov/pubmed/35784651 http://dx.doi.org/10.1016/j.crmeth.2022.100225 |
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