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Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive

CRISPR-based genetic engineering tools aimed to bias sex ratios, or drive effector genes into animal populations, often integrate the transgenes into autosomal chromosomes. However, in species with heterogametic sex chromsomes (e.g. XY, ZW), sex linkage of endonucleases could be beneficial to drive...

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Autores principales: Gamez, Stephanie, Chaverra-Rodriguez, Duverney, Buchman, Anna, Kandul, Nikolay P., Mendez-Sanchez, Stelia C., Bennett, Jared B., Sánchez C., Héctor M., Yang, Ting, Antoshechkin, Igor, Duque, Jonny E., Papathanos, Philippos A., Marshall, John M., Akbari, Omar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664916/
https://www.ncbi.nlm.nih.gov/pubmed/34893590
http://dx.doi.org/10.1038/s41467-021-27333-1
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author Gamez, Stephanie
Chaverra-Rodriguez, Duverney
Buchman, Anna
Kandul, Nikolay P.
Mendez-Sanchez, Stelia C.
Bennett, Jared B.
Sánchez C., Héctor M.
Yang, Ting
Antoshechkin, Igor
Duque, Jonny E.
Papathanos, Philippos A.
Marshall, John M.
Akbari, Omar S.
author_facet Gamez, Stephanie
Chaverra-Rodriguez, Duverney
Buchman, Anna
Kandul, Nikolay P.
Mendez-Sanchez, Stelia C.
Bennett, Jared B.
Sánchez C., Héctor M.
Yang, Ting
Antoshechkin, Igor
Duque, Jonny E.
Papathanos, Philippos A.
Marshall, John M.
Akbari, Omar S.
author_sort Gamez, Stephanie
collection PubMed
description CRISPR-based genetic engineering tools aimed to bias sex ratios, or drive effector genes into animal populations, often integrate the transgenes into autosomal chromosomes. However, in species with heterogametic sex chromsomes (e.g. XY, ZW), sex linkage of endonucleases could be beneficial to drive the expression in a sex-specific manner to produce genetic sexing systems, sex ratio distorters, or even sex-specific gene drives, for example. To explore this possibility, here we develop a transgenic line of Drosophila melanogaster expressing Cas9 from the Y chromosome. We functionally characterize the utility of this strain for both sex selection and gene drive finding it to be quite effective. To explore its utility for population control, we built mathematical models illustrating its dynamics as compared to other state-of-the-art systems designed for both population modification and suppression. Taken together, our results contribute to the development of current CRISPR genetic control tools and demonstrate the utility of using sex-linked Cas9 strains for genetic control of animals.
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spelling pubmed-86649162021-12-27 Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive Gamez, Stephanie Chaverra-Rodriguez, Duverney Buchman, Anna Kandul, Nikolay P. Mendez-Sanchez, Stelia C. Bennett, Jared B. Sánchez C., Héctor M. Yang, Ting Antoshechkin, Igor Duque, Jonny E. Papathanos, Philippos A. Marshall, John M. Akbari, Omar S. Nat Commun Article CRISPR-based genetic engineering tools aimed to bias sex ratios, or drive effector genes into animal populations, often integrate the transgenes into autosomal chromosomes. However, in species with heterogametic sex chromsomes (e.g. XY, ZW), sex linkage of endonucleases could be beneficial to drive the expression in a sex-specific manner to produce genetic sexing systems, sex ratio distorters, or even sex-specific gene drives, for example. To explore this possibility, here we develop a transgenic line of Drosophila melanogaster expressing Cas9 from the Y chromosome. We functionally characterize the utility of this strain for both sex selection and gene drive finding it to be quite effective. To explore its utility for population control, we built mathematical models illustrating its dynamics as compared to other state-of-the-art systems designed for both population modification and suppression. Taken together, our results contribute to the development of current CRISPR genetic control tools and demonstrate the utility of using sex-linked Cas9 strains for genetic control of animals. Nature Publishing Group UK 2021-12-10 /pmc/articles/PMC8664916/ /pubmed/34893590 http://dx.doi.org/10.1038/s41467-021-27333-1 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
Gamez, Stephanie
Chaverra-Rodriguez, Duverney
Buchman, Anna
Kandul, Nikolay P.
Mendez-Sanchez, Stelia C.
Bennett, Jared B.
Sánchez C., Héctor M.
Yang, Ting
Antoshechkin, Igor
Duque, Jonny E.
Papathanos, Philippos A.
Marshall, John M.
Akbari, Omar S.
Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive
title Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive
title_full Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive
title_fullStr Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive
title_full_unstemmed Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive
title_short Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive
title_sort exploiting a y chromosome-linked cas9 for sex selection and gene drive
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664916/
https://www.ncbi.nlm.nih.gov/pubmed/34893590
http://dx.doi.org/10.1038/s41467-021-27333-1
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