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Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR

Anopheles mosquitoes transmit at least 200 million annual malaria infections worldwide. Despite considerable genomic resources, mechanistic understanding of biological processes in Anopheles has been hampered by a lack of tools for reverse genetics. Here, we report successful application of the CRIS...

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Detalles Bibliográficos
Autores principales: Li, Ming, Akbari, Omar S., White, Bradley J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919725/
https://www.ncbi.nlm.nih.gov/pubmed/29233915
http://dx.doi.org/10.1534/g3.117.1134
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author Li, Ming
Akbari, Omar S.
White, Bradley J.
author_facet Li, Ming
Akbari, Omar S.
White, Bradley J.
author_sort Li, Ming
collection PubMed
description Anopheles mosquitoes transmit at least 200 million annual malaria infections worldwide. Despite considerable genomic resources, mechanistic understanding of biological processes in Anopheles has been hampered by a lack of tools for reverse genetics. Here, we report successful application of the CRISPR/Cas9 system for highly efficient, site-specific mutagenesis in the diverse malaria vectors Anopheles albimanus, A. coluzzii, and A. funestus. When guide RNAs (gRNAs) and Cas9 protein are injected at high concentration, germline mutations are common and usually biallelic, allowing for the rapid creation of stable mutant lines for reverse genetic analysis. Our protocol should enable researchers to dissect the molecular and cellular basis of anopheline traits critical to successful disease transmission, potentially exposing new targets for malaria control.
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spelling pubmed-59197252018-04-27 Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR Li, Ming Akbari, Omar S. White, Bradley J. G3 (Bethesda) Investigations Anopheles mosquitoes transmit at least 200 million annual malaria infections worldwide. Despite considerable genomic resources, mechanistic understanding of biological processes in Anopheles has been hampered by a lack of tools for reverse genetics. Here, we report successful application of the CRISPR/Cas9 system for highly efficient, site-specific mutagenesis in the diverse malaria vectors Anopheles albimanus, A. coluzzii, and A. funestus. When guide RNAs (gRNAs) and Cas9 protein are injected at high concentration, germline mutations are common and usually biallelic, allowing for the rapid creation of stable mutant lines for reverse genetic analysis. Our protocol should enable researchers to dissect the molecular and cellular basis of anopheline traits critical to successful disease transmission, potentially exposing new targets for malaria control. Genetics Society of America 2017-12-11 /pmc/articles/PMC5919725/ /pubmed/29233915 http://dx.doi.org/10.1534/g3.117.1134 Text en Copyright © 2018 Li et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article 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 the original work is properly cited.
spellingShingle Investigations
Li, Ming
Akbari, Omar S.
White, Bradley J.
Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR
title Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR
title_full Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR
title_fullStr Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR
title_full_unstemmed Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR
title_short Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR
title_sort highly efficient site-specific mutagenesis in malaria mosquitoes using crispr
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919725/
https://www.ncbi.nlm.nih.gov/pubmed/29233915
http://dx.doi.org/10.1534/g3.117.1134
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