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CRISPR/Cas12a mediated knock-in of the Polled Celtic variant to produce a polled genotype in dairy cattle

In modern livestock farming horned cattle pose an increased risk of injury for each other as well as for the farmers. Dehorning without anesthesia is associated with stress and pain for the calves and raises concerns regarding animal welfare. Naturally occurring structural variants causing pollednes...

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Autores principales: Schuster, Felix, Aldag, Patrick, Frenzel, Antje, Hadeler, Klaus-Gerd, Lucas-Hahn, Andrea, Niemann, Heiner, Petersen, Björn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419524/
https://www.ncbi.nlm.nih.gov/pubmed/32782385
http://dx.doi.org/10.1038/s41598-020-70531-y
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author Schuster, Felix
Aldag, Patrick
Frenzel, Antje
Hadeler, Klaus-Gerd
Lucas-Hahn, Andrea
Niemann, Heiner
Petersen, Björn
author_facet Schuster, Felix
Aldag, Patrick
Frenzel, Antje
Hadeler, Klaus-Gerd
Lucas-Hahn, Andrea
Niemann, Heiner
Petersen, Björn
author_sort Schuster, Felix
collection PubMed
description In modern livestock farming horned cattle pose an increased risk of injury for each other as well as for the farmers. Dehorning without anesthesia is associated with stress and pain for the calves and raises concerns regarding animal welfare. Naturally occurring structural variants causing polledness are known for most beef cattle but are rare within the dairy cattle population. The most common structural variant in beef cattle consists of a 202 base pair insertion-deletion (Polled Celtic variant). For the generation of polled offspring from a horned Holstein–Friesian bull, we isolated the Polled Celtic variant from the genome of an Angus cow and integrated it into the genome of fibroblasts taken from the horned bull using the CRISPR/Cas12a system (formerly Cpf1). Modified fibroblasts served as donor cells for somatic cell nuclear transfer and reconstructed embryos were transferred into synchronized recipients. One resulting pregnancy was terminated on day 90 of gestation for the examination of the fetus. Macroscopic and histological analyses proved a polled phenotype. The remaining pregnancy was carried to term and delivered one calf with a polled phenotype which died shortly after birth. In conclusion, we successfully demonstrated the practical application of CRISPR/Cas12a in farm animal breeding and husbandry.
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spelling pubmed-74195242020-08-13 CRISPR/Cas12a mediated knock-in of the Polled Celtic variant to produce a polled genotype in dairy cattle Schuster, Felix Aldag, Patrick Frenzel, Antje Hadeler, Klaus-Gerd Lucas-Hahn, Andrea Niemann, Heiner Petersen, Björn Sci Rep Article In modern livestock farming horned cattle pose an increased risk of injury for each other as well as for the farmers. Dehorning without anesthesia is associated with stress and pain for the calves and raises concerns regarding animal welfare. Naturally occurring structural variants causing polledness are known for most beef cattle but are rare within the dairy cattle population. The most common structural variant in beef cattle consists of a 202 base pair insertion-deletion (Polled Celtic variant). For the generation of polled offspring from a horned Holstein–Friesian bull, we isolated the Polled Celtic variant from the genome of an Angus cow and integrated it into the genome of fibroblasts taken from the horned bull using the CRISPR/Cas12a system (formerly Cpf1). Modified fibroblasts served as donor cells for somatic cell nuclear transfer and reconstructed embryos were transferred into synchronized recipients. One resulting pregnancy was terminated on day 90 of gestation for the examination of the fetus. Macroscopic and histological analyses proved a polled phenotype. The remaining pregnancy was carried to term and delivered one calf with a polled phenotype which died shortly after birth. In conclusion, we successfully demonstrated the practical application of CRISPR/Cas12a in farm animal breeding and husbandry. Nature Publishing Group UK 2020-08-11 /pmc/articles/PMC7419524/ /pubmed/32782385 http://dx.doi.org/10.1038/s41598-020-70531-y Text en © The Author(s) 2020 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
Schuster, Felix
Aldag, Patrick
Frenzel, Antje
Hadeler, Klaus-Gerd
Lucas-Hahn, Andrea
Niemann, Heiner
Petersen, Björn
CRISPR/Cas12a mediated knock-in of the Polled Celtic variant to produce a polled genotype in dairy cattle
title CRISPR/Cas12a mediated knock-in of the Polled Celtic variant to produce a polled genotype in dairy cattle
title_full CRISPR/Cas12a mediated knock-in of the Polled Celtic variant to produce a polled genotype in dairy cattle
title_fullStr CRISPR/Cas12a mediated knock-in of the Polled Celtic variant to produce a polled genotype in dairy cattle
title_full_unstemmed CRISPR/Cas12a mediated knock-in of the Polled Celtic variant to produce a polled genotype in dairy cattle
title_short CRISPR/Cas12a mediated knock-in of the Polled Celtic variant to produce a polled genotype in dairy cattle
title_sort crispr/cas12a mediated knock-in of the polled celtic variant to produce a polled genotype in dairy cattle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419524/
https://www.ncbi.nlm.nih.gov/pubmed/32782385
http://dx.doi.org/10.1038/s41598-020-70531-y
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