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Application of CRISPR genetic screens to investigate neurological diseases
The adoption of CRISPR-Cas9 technology for functional genetic screens has been a transformative advance. Due to its modular nature, this technology can be customized to address a myriad of questions. To date, pooled, genome-scale studies have uncovered genes responsible for survival, proliferation,...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857349/ https://www.ncbi.nlm.nih.gov/pubmed/31727120 http://dx.doi.org/10.1186/s13024-019-0343-3 |
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author | So, Raphaella W. L. Chung, Sai Wai Lau, Heather H. C. Watts, Jeremy J. Gaudette, Erin Al-Azzawi, Zaid A. M. Bishay, Jossana Lin, Lilian Tsai-Wei Joung, Julia Wang, Xinzhu Schmitt-Ulms, Gerold |
author_facet | So, Raphaella W. L. Chung, Sai Wai Lau, Heather H. C. Watts, Jeremy J. Gaudette, Erin Al-Azzawi, Zaid A. M. Bishay, Jossana Lin, Lilian Tsai-Wei Joung, Julia Wang, Xinzhu Schmitt-Ulms, Gerold |
author_sort | So, Raphaella W. L. |
collection | PubMed |
description | The adoption of CRISPR-Cas9 technology for functional genetic screens has been a transformative advance. Due to its modular nature, this technology can be customized to address a myriad of questions. To date, pooled, genome-scale studies have uncovered genes responsible for survival, proliferation, drug resistance, viral susceptibility, and many other functions. The technology has even been applied to the functional interrogation of the non-coding genome. However, applications of this technology to neurological diseases remain scarce. This shortfall motivated the assembly of a review that will hopefully help researchers moving in this direction find their footing. The emphasis here will be on design considerations and concepts underlying this methodology. We will highlight groundbreaking studies in the CRISPR-Cas9 functional genetics field and discuss strengths and limitations of this technology for neurological disease applications. Finally, we will provide practical guidance on navigating the many choices that need to be made when implementing a CRISPR-Cas9 functional genetic screen for the study of neurological diseases. |
format | Online Article Text |
id | pubmed-6857349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68573492019-12-05 Application of CRISPR genetic screens to investigate neurological diseases So, Raphaella W. L. Chung, Sai Wai Lau, Heather H. C. Watts, Jeremy J. Gaudette, Erin Al-Azzawi, Zaid A. M. Bishay, Jossana Lin, Lilian Tsai-Wei Joung, Julia Wang, Xinzhu Schmitt-Ulms, Gerold Mol Neurodegener Review The adoption of CRISPR-Cas9 technology for functional genetic screens has been a transformative advance. Due to its modular nature, this technology can be customized to address a myriad of questions. To date, pooled, genome-scale studies have uncovered genes responsible for survival, proliferation, drug resistance, viral susceptibility, and many other functions. The technology has even been applied to the functional interrogation of the non-coding genome. However, applications of this technology to neurological diseases remain scarce. This shortfall motivated the assembly of a review that will hopefully help researchers moving in this direction find their footing. The emphasis here will be on design considerations and concepts underlying this methodology. We will highlight groundbreaking studies in the CRISPR-Cas9 functional genetics field and discuss strengths and limitations of this technology for neurological disease applications. Finally, we will provide practical guidance on navigating the many choices that need to be made when implementing a CRISPR-Cas9 functional genetic screen for the study of neurological diseases. BioMed Central 2019-11-14 /pmc/articles/PMC6857349/ /pubmed/31727120 http://dx.doi.org/10.1186/s13024-019-0343-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review So, Raphaella W. L. Chung, Sai Wai Lau, Heather H. C. Watts, Jeremy J. Gaudette, Erin Al-Azzawi, Zaid A. M. Bishay, Jossana Lin, Lilian Tsai-Wei Joung, Julia Wang, Xinzhu Schmitt-Ulms, Gerold Application of CRISPR genetic screens to investigate neurological diseases |
title | Application of CRISPR genetic screens to investigate neurological diseases |
title_full | Application of CRISPR genetic screens to investigate neurological diseases |
title_fullStr | Application of CRISPR genetic screens to investigate neurological diseases |
title_full_unstemmed | Application of CRISPR genetic screens to investigate neurological diseases |
title_short | Application of CRISPR genetic screens to investigate neurological diseases |
title_sort | application of crispr genetic screens to investigate neurological diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857349/ https://www.ncbi.nlm.nih.gov/pubmed/31727120 http://dx.doi.org/10.1186/s13024-019-0343-3 |
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