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Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation
CRISPR-based homing gene drives can be designed to disrupt essential genes whilst biasing their own inheritance, leading to suppression of mosquito populations in the laboratory. This class of gene drives relies on CRISPR-Cas9 cleavage of a target sequence and copying (‘homing’) therein of the gene...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519452/ https://www.ncbi.nlm.nih.gov/pubmed/34610011 http://dx.doi.org/10.1371/journal.pgen.1009740 |
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author | Fuchs, Silke Garrood, William T. Beber, Anna Hammond, Andrew Galizi, Roberto Gribble, Matthew Morselli, Giulia Hui, Tin-Yu J. Willis, Katie Kranjc, Nace Burt, Austin Crisanti, Andrea Nolan, Tony |
author_facet | Fuchs, Silke Garrood, William T. Beber, Anna Hammond, Andrew Galizi, Roberto Gribble, Matthew Morselli, Giulia Hui, Tin-Yu J. Willis, Katie Kranjc, Nace Burt, Austin Crisanti, Andrea Nolan, Tony |
author_sort | Fuchs, Silke |
collection | PubMed |
description | CRISPR-based homing gene drives can be designed to disrupt essential genes whilst biasing their own inheritance, leading to suppression of mosquito populations in the laboratory. This class of gene drives relies on CRISPR-Cas9 cleavage of a target sequence and copying (‘homing’) therein of the gene drive element from the homologous chromosome. However, target site mutations that are resistant to cleavage yet maintain the function of the essential gene are expected to be strongly selected for. Targeting functionally constrained regions where mutations are not easily tolerated should lower the probability of resistance. Evolutionary conservation at the sequence level is often a reliable indicator of functional constraint, though the actual level of underlying constraint between one conserved sequence and another can vary widely. Here we generated a novel adult lethal gene drive (ALGD) in the malaria vector Anopheles gambiae, targeting an ultra-conserved target site in a haplosufficient essential gene (AGAP029113) required during mosquito development, which fulfils many of the criteria for the target of a population suppression gene drive. We then designed a selection regime to experimentally assess the likelihood of generation and subsequent selection of gene drive resistant mutations at its target site. We simulated, in a caged population, a scenario where the gene drive was approaching fixation, where selection for resistance is expected to be strongest. Continuous sampling of the target locus revealed that a single, restorative, in-frame nucleotide substitution was selected. Our findings show that ultra-conservation alone need not be predictive of a site that is refractory to target site resistance. Our strategy to evaluate resistance in vivo could help to validate candidate gene drive targets for their resilience to resistance and help to improve predictions of the invasion dynamics of gene drives in field populations. |
format | Online Article Text |
id | pubmed-8519452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-85194522021-10-16 Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation Fuchs, Silke Garrood, William T. Beber, Anna Hammond, Andrew Galizi, Roberto Gribble, Matthew Morselli, Giulia Hui, Tin-Yu J. Willis, Katie Kranjc, Nace Burt, Austin Crisanti, Andrea Nolan, Tony PLoS Genet Research Article CRISPR-based homing gene drives can be designed to disrupt essential genes whilst biasing their own inheritance, leading to suppression of mosquito populations in the laboratory. This class of gene drives relies on CRISPR-Cas9 cleavage of a target sequence and copying (‘homing’) therein of the gene drive element from the homologous chromosome. However, target site mutations that are resistant to cleavage yet maintain the function of the essential gene are expected to be strongly selected for. Targeting functionally constrained regions where mutations are not easily tolerated should lower the probability of resistance. Evolutionary conservation at the sequence level is often a reliable indicator of functional constraint, though the actual level of underlying constraint between one conserved sequence and another can vary widely. Here we generated a novel adult lethal gene drive (ALGD) in the malaria vector Anopheles gambiae, targeting an ultra-conserved target site in a haplosufficient essential gene (AGAP029113) required during mosquito development, which fulfils many of the criteria for the target of a population suppression gene drive. We then designed a selection regime to experimentally assess the likelihood of generation and subsequent selection of gene drive resistant mutations at its target site. We simulated, in a caged population, a scenario where the gene drive was approaching fixation, where selection for resistance is expected to be strongest. Continuous sampling of the target locus revealed that a single, restorative, in-frame nucleotide substitution was selected. Our findings show that ultra-conservation alone need not be predictive of a site that is refractory to target site resistance. Our strategy to evaluate resistance in vivo could help to validate candidate gene drive targets for their resilience to resistance and help to improve predictions of the invasion dynamics of gene drives in field populations. Public Library of Science 2021-10-05 /pmc/articles/PMC8519452/ /pubmed/34610011 http://dx.doi.org/10.1371/journal.pgen.1009740 Text en © 2021 Fuchs et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Fuchs, Silke Garrood, William T. Beber, Anna Hammond, Andrew Galizi, Roberto Gribble, Matthew Morselli, Giulia Hui, Tin-Yu J. Willis, Katie Kranjc, Nace Burt, Austin Crisanti, Andrea Nolan, Tony Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation |
title | Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation |
title_full | Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation |
title_fullStr | Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation |
title_full_unstemmed | Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation |
title_short | Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation |
title_sort | resistance to a crispr-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519452/ https://www.ncbi.nlm.nih.gov/pubmed/34610011 http://dx.doi.org/10.1371/journal.pgen.1009740 |
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