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A genetically encoded anti-CRISPR protein constrains gene drive spread and prevents population suppression

CRISPR-based gene drives offer promising means to reduce the burden of pests and vector-borne diseases. These techniques consist of releasing genetically modified organisms carrying CRISPR-Cas nucleases designed to bias their inheritance and rapidly propagate desired modifications. Gene drives can b...

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Autores principales: Taxiarchi, Chrysanthi, Beaghton, Andrea, Don, Nayomi Illansinhage, Kyrou, Kyros, Gribble, Matthew, Shittu, Dammy, Collins, Scott P., Beisel, Chase L., Galizi, Roberto, Crisanti, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233359/
https://www.ncbi.nlm.nih.gov/pubmed/34172748
http://dx.doi.org/10.1038/s41467-021-24214-5
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author Taxiarchi, Chrysanthi
Beaghton, Andrea
Don, Nayomi Illansinhage
Kyrou, Kyros
Gribble, Matthew
Shittu, Dammy
Collins, Scott P.
Beisel, Chase L.
Galizi, Roberto
Crisanti, Andrea
author_facet Taxiarchi, Chrysanthi
Beaghton, Andrea
Don, Nayomi Illansinhage
Kyrou, Kyros
Gribble, Matthew
Shittu, Dammy
Collins, Scott P.
Beisel, Chase L.
Galizi, Roberto
Crisanti, Andrea
author_sort Taxiarchi, Chrysanthi
collection PubMed
description CRISPR-based gene drives offer promising means to reduce the burden of pests and vector-borne diseases. These techniques consist of releasing genetically modified organisms carrying CRISPR-Cas nucleases designed to bias their inheritance and rapidly propagate desired modifications. Gene drives can be intended to reduce reproductive capacity of harmful insects or spread anti-pathogen effectors through wild populations, even when these confer fitness disadvantages. Technologies capable of halting the spread of gene drives may prove highly valuable in controlling, counteracting, and even reverting their effect on individual organisms as well as entire populations. Here we show engineering and testing of a genetic approach, based on the germline expression of a phage-derived anti-CRISPR protein (AcrIIA4), able to inactivate CRISPR-based gene drives and restore their inheritance to Mendelian rates in the malaria vector Anopheles gambiae. Modeling predictions and cage testing show that a single release of male mosquitoes carrying the AcrIIA4 protein can block the spread of a highly effective suppressive gene drive preventing population collapse of caged malaria mosquitoes.
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spelling pubmed-82333592021-07-09 A genetically encoded anti-CRISPR protein constrains gene drive spread and prevents population suppression Taxiarchi, Chrysanthi Beaghton, Andrea Don, Nayomi Illansinhage Kyrou, Kyros Gribble, Matthew Shittu, Dammy Collins, Scott P. Beisel, Chase L. Galizi, Roberto Crisanti, Andrea Nat Commun Article CRISPR-based gene drives offer promising means to reduce the burden of pests and vector-borne diseases. These techniques consist of releasing genetically modified organisms carrying CRISPR-Cas nucleases designed to bias their inheritance and rapidly propagate desired modifications. Gene drives can be intended to reduce reproductive capacity of harmful insects or spread anti-pathogen effectors through wild populations, even when these confer fitness disadvantages. Technologies capable of halting the spread of gene drives may prove highly valuable in controlling, counteracting, and even reverting their effect on individual organisms as well as entire populations. Here we show engineering and testing of a genetic approach, based on the germline expression of a phage-derived anti-CRISPR protein (AcrIIA4), able to inactivate CRISPR-based gene drives and restore their inheritance to Mendelian rates in the malaria vector Anopheles gambiae. Modeling predictions and cage testing show that a single release of male mosquitoes carrying the AcrIIA4 protein can block the spread of a highly effective suppressive gene drive preventing population collapse of caged malaria mosquitoes. Nature Publishing Group UK 2021-06-25 /pmc/articles/PMC8233359/ /pubmed/34172748 http://dx.doi.org/10.1038/s41467-021-24214-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Taxiarchi, Chrysanthi
Beaghton, Andrea
Don, Nayomi Illansinhage
Kyrou, Kyros
Gribble, Matthew
Shittu, Dammy
Collins, Scott P.
Beisel, Chase L.
Galizi, Roberto
Crisanti, Andrea
A genetically encoded anti-CRISPR protein constrains gene drive spread and prevents population suppression
title A genetically encoded anti-CRISPR protein constrains gene drive spread and prevents population suppression
title_full A genetically encoded anti-CRISPR protein constrains gene drive spread and prevents population suppression
title_fullStr A genetically encoded anti-CRISPR protein constrains gene drive spread and prevents population suppression
title_full_unstemmed A genetically encoded anti-CRISPR protein constrains gene drive spread and prevents population suppression
title_short A genetically encoded anti-CRISPR protein constrains gene drive spread and prevents population suppression
title_sort genetically encoded anti-crispr protein constrains gene drive spread and prevents population suppression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233359/
https://www.ncbi.nlm.nih.gov/pubmed/34172748
http://dx.doi.org/10.1038/s41467-021-24214-5
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