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Medusa: A Novel Gene Drive System for Confined Suppression of Insect Populations
Gene drive systems provide novel opportunities for insect population suppression by driving genes that confer a fitness cost into pest or disease vector populations; however regulatory issues arise when genes are capable of spreading across international borders. Gene drive systems displaying thresh...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108329/ https://www.ncbi.nlm.nih.gov/pubmed/25054803 http://dx.doi.org/10.1371/journal.pone.0102694 |
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author | Marshall, John M. Hay, Bruce A. |
author_facet | Marshall, John M. Hay, Bruce A. |
author_sort | Marshall, John M. |
collection | PubMed |
description | Gene drive systems provide novel opportunities for insect population suppression by driving genes that confer a fitness cost into pest or disease vector populations; however regulatory issues arise when genes are capable of spreading across international borders. Gene drive systems displaying threshold properties provide a solution since they can be confined to local populations and eliminated through dilution with wild-types. We propose a novel, threshold-dependent gene drive system, Medusa, capable of inducing a local and reversible population crash. Medusa consists of four components - two on the X chromosome, and two on the Y chromosome. A maternally-expressed, X-linked toxin and a zygotically-expressed, Y-linked antidote results in suppression of the female population and selection for the presence of the transgene-bearing Y because only male offspring of Medusa-bearing females are protected from the effects of the toxin. At the same time, the combination of a zygotically-expressed, Y-linked toxin and a zygotically-expressed, X-linked antidote selects for the transgene-bearing X in the presence of the transgene-bearing Y. Together these chromosomes create a balanced lethal system that spreads while selecting against females when present above a certain threshold frequency. Simple population dynamic models show that an all-male release of Medusa males, carried out over six generations, is expected to induce a population crash within 12 generations for modest release sizes on the order of the wild population size. Re-invasion of non-transgenic insects into a suppressed population can result in a population rebound; however this can be prevented through regular releases of modest numbers of Medusa males. Finally, we outline how Medusa could be engineered with currently available molecular tools. |
format | Online Article Text |
id | pubmed-4108329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41083292014-07-24 Medusa: A Novel Gene Drive System for Confined Suppression of Insect Populations Marshall, John M. Hay, Bruce A. PLoS One Research Article Gene drive systems provide novel opportunities for insect population suppression by driving genes that confer a fitness cost into pest or disease vector populations; however regulatory issues arise when genes are capable of spreading across international borders. Gene drive systems displaying threshold properties provide a solution since they can be confined to local populations and eliminated through dilution with wild-types. We propose a novel, threshold-dependent gene drive system, Medusa, capable of inducing a local and reversible population crash. Medusa consists of four components - two on the X chromosome, and two on the Y chromosome. A maternally-expressed, X-linked toxin and a zygotically-expressed, Y-linked antidote results in suppression of the female population and selection for the presence of the transgene-bearing Y because only male offspring of Medusa-bearing females are protected from the effects of the toxin. At the same time, the combination of a zygotically-expressed, Y-linked toxin and a zygotically-expressed, X-linked antidote selects for the transgene-bearing X in the presence of the transgene-bearing Y. Together these chromosomes create a balanced lethal system that spreads while selecting against females when present above a certain threshold frequency. Simple population dynamic models show that an all-male release of Medusa males, carried out over six generations, is expected to induce a population crash within 12 generations for modest release sizes on the order of the wild population size. Re-invasion of non-transgenic insects into a suppressed population can result in a population rebound; however this can be prevented through regular releases of modest numbers of Medusa males. Finally, we outline how Medusa could be engineered with currently available molecular tools. Public Library of Science 2014-07-23 /pmc/articles/PMC4108329/ /pubmed/25054803 http://dx.doi.org/10.1371/journal.pone.0102694 Text en © 2014 Marshall, Hay http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Marshall, John M. Hay, Bruce A. Medusa: A Novel Gene Drive System for Confined Suppression of Insect Populations |
title |
Medusa: A Novel Gene Drive System for Confined Suppression of Insect Populations |
title_full |
Medusa: A Novel Gene Drive System for Confined Suppression of Insect Populations |
title_fullStr |
Medusa: A Novel Gene Drive System for Confined Suppression of Insect Populations |
title_full_unstemmed |
Medusa: A Novel Gene Drive System for Confined Suppression of Insect Populations |
title_short |
Medusa: A Novel Gene Drive System for Confined Suppression of Insect Populations |
title_sort | medusa: a novel gene drive system for confined suppression of insect populations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108329/ https://www.ncbi.nlm.nih.gov/pubmed/25054803 http://dx.doi.org/10.1371/journal.pone.0102694 |
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