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Mathematical modeling of self-contained CRISPR gene drive reversal systems

There is a critical need for further research into methods to control biological populations. Numerous challenges to agriculture, ecological systems, and human health could be mitigated by the targeted reduction and management of key species (e.g. pests, parasites, and vectors for pathogens). The di...

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Autores principales: Heffel, Matthew G., Finnigan, Gregory C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934693/
https://www.ncbi.nlm.nih.gov/pubmed/31882576
http://dx.doi.org/10.1038/s41598-019-54805-8
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author Heffel, Matthew G.
Finnigan, Gregory C.
author_facet Heffel, Matthew G.
Finnigan, Gregory C.
author_sort Heffel, Matthew G.
collection PubMed
description There is a critical need for further research into methods to control biological populations. Numerous challenges to agriculture, ecological systems, and human health could be mitigated by the targeted reduction and management of key species (e.g. pests, parasites, and vectors for pathogens). The discovery and adaptation of the CRISPR/Cas editing platform co-opted from bacteria has provided a mechanism for a means to alter an entire population. A CRISPR-based gene drive system can allow for the forced propagation of a genetic element that bypasses Mendelian inheritance which can be used to bias sex determination, install exogenous information, or remove endogenous DNA within an entire species. Laboratory studies have demonstrated the potency by which gene drives can operate within insects and other organisms. However, continued research and eventual application face serious opposition regarding issues of policy, biosafety, effectiveness, and reversal. Previous mathematical work has suggested the use of modified gene drive designs that are limited in spread such as daisy chain or underdominance drives. However, no system has yet been proposed that allows for an inducible reversal mechanism without requiring the introduction of additional individuals. Here, we study gene drive effectiveness, fitness, and inducible drive systems that could respond to external stimuli expanding from a previous frequency-based population model. We find that programmed modification during gene drive propagation could serve as a potent safeguard to either slow or completely reverse drive systems and allow for a return to the original wild-type population.
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spelling pubmed-69346932019-12-30 Mathematical modeling of self-contained CRISPR gene drive reversal systems Heffel, Matthew G. Finnigan, Gregory C. Sci Rep Article There is a critical need for further research into methods to control biological populations. Numerous challenges to agriculture, ecological systems, and human health could be mitigated by the targeted reduction and management of key species (e.g. pests, parasites, and vectors for pathogens). The discovery and adaptation of the CRISPR/Cas editing platform co-opted from bacteria has provided a mechanism for a means to alter an entire population. A CRISPR-based gene drive system can allow for the forced propagation of a genetic element that bypasses Mendelian inheritance which can be used to bias sex determination, install exogenous information, or remove endogenous DNA within an entire species. Laboratory studies have demonstrated the potency by which gene drives can operate within insects and other organisms. However, continued research and eventual application face serious opposition regarding issues of policy, biosafety, effectiveness, and reversal. Previous mathematical work has suggested the use of modified gene drive designs that are limited in spread such as daisy chain or underdominance drives. However, no system has yet been proposed that allows for an inducible reversal mechanism without requiring the introduction of additional individuals. Here, we study gene drive effectiveness, fitness, and inducible drive systems that could respond to external stimuli expanding from a previous frequency-based population model. We find that programmed modification during gene drive propagation could serve as a potent safeguard to either slow or completely reverse drive systems and allow for a return to the original wild-type population. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934693/ /pubmed/31882576 http://dx.doi.org/10.1038/s41598-019-54805-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Heffel, Matthew G.
Finnigan, Gregory C.
Mathematical modeling of self-contained CRISPR gene drive reversal systems
title Mathematical modeling of self-contained CRISPR gene drive reversal systems
title_full Mathematical modeling of self-contained CRISPR gene drive reversal systems
title_fullStr Mathematical modeling of self-contained CRISPR gene drive reversal systems
title_full_unstemmed Mathematical modeling of self-contained CRISPR gene drive reversal systems
title_short Mathematical modeling of self-contained CRISPR gene drive reversal systems
title_sort mathematical modeling of self-contained crispr gene drive reversal systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934693/
https://www.ncbi.nlm.nih.gov/pubmed/31882576
http://dx.doi.org/10.1038/s41598-019-54805-8
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