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LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele

A long intergenic non-coding RNA (lincRNA#1) is overexpressed in the horn bud region of polled (hornless) bovine fetuses, suggesting a potential role in horn bud suppression. Genome editing was used to test whether the absence of this sequence was associated with the horned phenotype. Two gRNAs with...

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Autores principales: Hennig, Sadie L., McNabb, Bret R., Trott, Josephine F., Van Eenennaam, Alison L., Murray, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090918/
https://www.ncbi.nlm.nih.gov/pubmed/35538091
http://dx.doi.org/10.1038/s41598-022-11669-9
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author Hennig, Sadie L.
McNabb, Bret R.
Trott, Josephine F.
Van Eenennaam, Alison L.
Murray, James D.
author_facet Hennig, Sadie L.
McNabb, Bret R.
Trott, Josephine F.
Van Eenennaam, Alison L.
Murray, James D.
author_sort Hennig, Sadie L.
collection PubMed
description A long intergenic non-coding RNA (lincRNA#1) is overexpressed in the horn bud region of polled (hornless) bovine fetuses, suggesting a potential role in horn bud suppression. Genome editing was used to test whether the absence of this sequence was associated with the horned phenotype. Two gRNAs with high mutation efficiencies targeting the 5′ and the 3′ regions flanking the lincRNA#1 sequence were co-injected with Cas9 as ribonucleoprotein complexes into bovine zygotes (n = 121) 6 h post insemination. Of the resulting blastocysts (n = 31), 84% had the expected 3.7 kb deletion; of these embryos with the 3.7 kb deletions, 88% were biallelic knockouts. Thirty-nine presumptive edited 7-day blastocysts were transferred to 13 synchronized recipient cows resulting in ten pregnancies, five with embryos heterozygous for the dominant P(C) POLLED allele at the POLLED locus, and five with the recessive pp genotype. Eight (80%) of the resulting fetuses were biallelic lincRNA#1 knockouts, with the remaining two being mosaic. RT-qPCR analysis was used to confirm the absence of lincRNA#1 expression in knockout fetuses. Phenotypic and histological analysis of the genotypically (P(C)p) POLLED, lincRNA#1 knockout fetuses revealed similar morphology to non-edited, control polled fetuses, indicating the absence of lincRNA#1 alone does not result in a horned phenotype.
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spelling pubmed-90909182022-05-12 LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele Hennig, Sadie L. McNabb, Bret R. Trott, Josephine F. Van Eenennaam, Alison L. Murray, James D. Sci Rep Article A long intergenic non-coding RNA (lincRNA#1) is overexpressed in the horn bud region of polled (hornless) bovine fetuses, suggesting a potential role in horn bud suppression. Genome editing was used to test whether the absence of this sequence was associated with the horned phenotype. Two gRNAs with high mutation efficiencies targeting the 5′ and the 3′ regions flanking the lincRNA#1 sequence were co-injected with Cas9 as ribonucleoprotein complexes into bovine zygotes (n = 121) 6 h post insemination. Of the resulting blastocysts (n = 31), 84% had the expected 3.7 kb deletion; of these embryos with the 3.7 kb deletions, 88% were biallelic knockouts. Thirty-nine presumptive edited 7-day blastocysts were transferred to 13 synchronized recipient cows resulting in ten pregnancies, five with embryos heterozygous for the dominant P(C) POLLED allele at the POLLED locus, and five with the recessive pp genotype. Eight (80%) of the resulting fetuses were biallelic lincRNA#1 knockouts, with the remaining two being mosaic. RT-qPCR analysis was used to confirm the absence of lincRNA#1 expression in knockout fetuses. Phenotypic and histological analysis of the genotypically (P(C)p) POLLED, lincRNA#1 knockout fetuses revealed similar morphology to non-edited, control polled fetuses, indicating the absence of lincRNA#1 alone does not result in a horned phenotype. Nature Publishing Group UK 2022-05-10 /pmc/articles/PMC9090918/ /pubmed/35538091 http://dx.doi.org/10.1038/s41598-022-11669-9 Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hennig, Sadie L.
McNabb, Bret R.
Trott, Josephine F.
Van Eenennaam, Alison L.
Murray, James D.
LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele
title LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele
title_full LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele
title_fullStr LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele
title_full_unstemmed LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele
title_short LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele
title_sort lincrna#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic polled allele
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090918/
https://www.ncbi.nlm.nih.gov/pubmed/35538091
http://dx.doi.org/10.1038/s41598-022-11669-9
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