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Strategies to reduce genetic mosaicism following CRISPR-mediated genome edition in bovine embryos

Genetic mosaicism is the presence of more than two alleles on an individual and it is commonly observed following CRISPR microinjection of zygotes. This phenomenon appears when DNA replication precedes CRISPR-mediated genome edition and it is undesirable because it reduces greatly the odds for direc...

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Autores principales: Lamas-Toranzo, I., Galiano-Cogolludo, B., Cornudella-Ardiaca, F., Cobos-Figueroa, J., Ousinde, O., Bermejo-Álvarez, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797768/
https://www.ncbi.nlm.nih.gov/pubmed/31624292
http://dx.doi.org/10.1038/s41598-019-51366-8
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author Lamas-Toranzo, I.
Galiano-Cogolludo, B.
Cornudella-Ardiaca, F.
Cobos-Figueroa, J.
Ousinde, O.
Bermejo-Álvarez, P.
author_facet Lamas-Toranzo, I.
Galiano-Cogolludo, B.
Cornudella-Ardiaca, F.
Cobos-Figueroa, J.
Ousinde, O.
Bermejo-Álvarez, P.
author_sort Lamas-Toranzo, I.
collection PubMed
description Genetic mosaicism is the presence of more than two alleles on an individual and it is commonly observed following CRISPR microinjection of zygotes. This phenomenon appears when DNA replication precedes CRISPR-mediated genome edition and it is undesirable because it reduces greatly the odds for direct KO generation by randomly generated indels. In this study, we have developed alternative protocols to reduce mosaicism rates following CRISPR-mediated genome edition in bovine. In a preliminary study we observed by EdU incorporation that DNA replication has already occurred at the conventional microinjection time (20 hpi). Aiming to reduce mosaicism appearance, we have developed three alternative microinjection protocols: early zygote microinjection (10 hpi RNA) or oocyte microinjection before fertilization with either RNA or Ribonucleoprotein delivery (0 hpi RNA or 0 hpi RNP). All three alternative microinjection protocols resulted in similar blastocyst and genome edition rates compared to the conventional 20 hpi group, whereas mosaicism rates were significantly reduced in all early delivery groups (~10–30% of edited embryos being mosaic depending on the loci) compared to conventional 20 hpi microinjection (100% mosaicism rate). These strategies constitute an efficient way to reduce the number of indels, increasing the odds for direct KO generation.
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spelling pubmed-67977682019-10-25 Strategies to reduce genetic mosaicism following CRISPR-mediated genome edition in bovine embryos Lamas-Toranzo, I. Galiano-Cogolludo, B. Cornudella-Ardiaca, F. Cobos-Figueroa, J. Ousinde, O. Bermejo-Álvarez, P. Sci Rep Article Genetic mosaicism is the presence of more than two alleles on an individual and it is commonly observed following CRISPR microinjection of zygotes. This phenomenon appears when DNA replication precedes CRISPR-mediated genome edition and it is undesirable because it reduces greatly the odds for direct KO generation by randomly generated indels. In this study, we have developed alternative protocols to reduce mosaicism rates following CRISPR-mediated genome edition in bovine. In a preliminary study we observed by EdU incorporation that DNA replication has already occurred at the conventional microinjection time (20 hpi). Aiming to reduce mosaicism appearance, we have developed three alternative microinjection protocols: early zygote microinjection (10 hpi RNA) or oocyte microinjection before fertilization with either RNA or Ribonucleoprotein delivery (0 hpi RNA or 0 hpi RNP). All three alternative microinjection protocols resulted in similar blastocyst and genome edition rates compared to the conventional 20 hpi group, whereas mosaicism rates were significantly reduced in all early delivery groups (~10–30% of edited embryos being mosaic depending on the loci) compared to conventional 20 hpi microinjection (100% mosaicism rate). These strategies constitute an efficient way to reduce the number of indels, increasing the odds for direct KO generation. Nature Publishing Group UK 2019-10-17 /pmc/articles/PMC6797768/ /pubmed/31624292 http://dx.doi.org/10.1038/s41598-019-51366-8 Text en © The Author(s) 2019 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/.
spellingShingle Article
Lamas-Toranzo, I.
Galiano-Cogolludo, B.
Cornudella-Ardiaca, F.
Cobos-Figueroa, J.
Ousinde, O.
Bermejo-Álvarez, P.
Strategies to reduce genetic mosaicism following CRISPR-mediated genome edition in bovine embryos
title Strategies to reduce genetic mosaicism following CRISPR-mediated genome edition in bovine embryos
title_full Strategies to reduce genetic mosaicism following CRISPR-mediated genome edition in bovine embryos
title_fullStr Strategies to reduce genetic mosaicism following CRISPR-mediated genome edition in bovine embryos
title_full_unstemmed Strategies to reduce genetic mosaicism following CRISPR-mediated genome edition in bovine embryos
title_short Strategies to reduce genetic mosaicism following CRISPR-mediated genome edition in bovine embryos
title_sort strategies to reduce genetic mosaicism following crispr-mediated genome edition in bovine embryos
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797768/
https://www.ncbi.nlm.nih.gov/pubmed/31624292
http://dx.doi.org/10.1038/s41598-019-51366-8
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