Cargando…
Insertion of an endogenous Jaagsiekte sheep retrovirus element into the BCO2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in Norwegian Spælsau (Ovis aries)
BACKGROUND: The accumulation of carotenoids in adipose tissue leading to yellow fat is, in sheep, a heritable recessive trait that can be attributed to a nonsense mutation in the beta-carotene oxygenase 2 (BCO2) gene. However, not all sheep breeds suffering from yellow fat have this nonsense mutatio...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247158/ https://www.ncbi.nlm.nih.gov/pubmed/34193038 http://dx.doi.org/10.1186/s12864-021-07826-5 |
_version_ | 1783716462961098752 |
---|---|
author | Kent, Matthew Moser, Michel Boman, Inger Anne Lindtveit, Kristine Árnyasi, Mariann Sundsaasen, Kristil Kindem Våge, Dag Inge |
author_facet | Kent, Matthew Moser, Michel Boman, Inger Anne Lindtveit, Kristine Árnyasi, Mariann Sundsaasen, Kristil Kindem Våge, Dag Inge |
author_sort | Kent, Matthew |
collection | PubMed |
description | BACKGROUND: The accumulation of carotenoids in adipose tissue leading to yellow fat is, in sheep, a heritable recessive trait that can be attributed to a nonsense mutation in the beta-carotene oxygenase 2 (BCO2) gene. However, not all sheep breeds suffering from yellow fat have this nonsense mutation, meaning that other functional mechanisms must exist. We investigated one such breed, the Norwegian spælsau. RESULTS: In spælsau we detected an aberration in BCO2 mRNA. Nanopore sequencing of genomic DNA revealed the insertion of a 7.9 kb endogenous Jaagsiekte Sheep Retrovirus (enJSRV) sequence in the first intron of the BCO2 gene. Close examination of its cDNA revealed that the BCO2 genes first exon was spliced together with enJSRV-sequence immediately downstream of a potential -AG splice acceptor site at enJSRV position 415. The hybrid protein product consists of 29 amino acids coded by the BCO2 exon 1, one amino acid coded by the junction sequence, followed by 28 amino acids arbitrary coded for by the enJSRV-sequence, before a translation stop codon is reached. CONCLUSIONS: Considering that the functional BCO2 protein consists of 575 amino acids, it is unlikely that the 58 amino acid BCO2/enJSRV hybrid protein can display any enzymatic function. The existence of this novel BCO2 allele represents an alternative functional mechanism accounting for BCO2 inactivation and is a perfect example of the potential benefits for searching for structural variants using long-read sequencing data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07826-5. |
format | Online Article Text |
id | pubmed-8247158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82471582021-07-06 Insertion of an endogenous Jaagsiekte sheep retrovirus element into the BCO2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in Norwegian Spælsau (Ovis aries) Kent, Matthew Moser, Michel Boman, Inger Anne Lindtveit, Kristine Árnyasi, Mariann Sundsaasen, Kristil Kindem Våge, Dag Inge BMC Genomics Research Article BACKGROUND: The accumulation of carotenoids in adipose tissue leading to yellow fat is, in sheep, a heritable recessive trait that can be attributed to a nonsense mutation in the beta-carotene oxygenase 2 (BCO2) gene. However, not all sheep breeds suffering from yellow fat have this nonsense mutation, meaning that other functional mechanisms must exist. We investigated one such breed, the Norwegian spælsau. RESULTS: In spælsau we detected an aberration in BCO2 mRNA. Nanopore sequencing of genomic DNA revealed the insertion of a 7.9 kb endogenous Jaagsiekte Sheep Retrovirus (enJSRV) sequence in the first intron of the BCO2 gene. Close examination of its cDNA revealed that the BCO2 genes first exon was spliced together with enJSRV-sequence immediately downstream of a potential -AG splice acceptor site at enJSRV position 415. The hybrid protein product consists of 29 amino acids coded by the BCO2 exon 1, one amino acid coded by the junction sequence, followed by 28 amino acids arbitrary coded for by the enJSRV-sequence, before a translation stop codon is reached. CONCLUSIONS: Considering that the functional BCO2 protein consists of 575 amino acids, it is unlikely that the 58 amino acid BCO2/enJSRV hybrid protein can display any enzymatic function. The existence of this novel BCO2 allele represents an alternative functional mechanism accounting for BCO2 inactivation and is a perfect example of the potential benefits for searching for structural variants using long-read sequencing data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07826-5. BioMed Central 2021-06-30 /pmc/articles/PMC8247158/ /pubmed/34193038 http://dx.doi.org/10.1186/s12864-021-07826-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Kent, Matthew Moser, Michel Boman, Inger Anne Lindtveit, Kristine Árnyasi, Mariann Sundsaasen, Kristil Kindem Våge, Dag Inge Insertion of an endogenous Jaagsiekte sheep retrovirus element into the BCO2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in Norwegian Spælsau (Ovis aries) |
title | Insertion of an endogenous Jaagsiekte sheep retrovirus element into the BCO2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in Norwegian Spælsau (Ovis aries) |
title_full | Insertion of an endogenous Jaagsiekte sheep retrovirus element into the BCO2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in Norwegian Spælsau (Ovis aries) |
title_fullStr | Insertion of an endogenous Jaagsiekte sheep retrovirus element into the BCO2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in Norwegian Spælsau (Ovis aries) |
title_full_unstemmed | Insertion of an endogenous Jaagsiekte sheep retrovirus element into the BCO2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in Norwegian Spælsau (Ovis aries) |
title_short | Insertion of an endogenous Jaagsiekte sheep retrovirus element into the BCO2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in Norwegian Spælsau (Ovis aries) |
title_sort | insertion of an endogenous jaagsiekte sheep retrovirus element into the bco2 - gene abolishes its function and leads to yellow discoloration of adipose tissue in norwegian spælsau (ovis aries) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247158/ https://www.ncbi.nlm.nih.gov/pubmed/34193038 http://dx.doi.org/10.1186/s12864-021-07826-5 |
work_keys_str_mv | AT kentmatthew insertionofanendogenousjaagsiektesheepretroviruselementintothebco2geneabolishesitsfunctionandleadstoyellowdiscolorationofadiposetissueinnorwegianspælsauovisaries AT mosermichel insertionofanendogenousjaagsiektesheepretroviruselementintothebco2geneabolishesitsfunctionandleadstoyellowdiscolorationofadiposetissueinnorwegianspælsauovisaries AT bomaningeranne insertionofanendogenousjaagsiektesheepretroviruselementintothebco2geneabolishesitsfunctionandleadstoyellowdiscolorationofadiposetissueinnorwegianspælsauovisaries AT lindtveitkristine insertionofanendogenousjaagsiektesheepretroviruselementintothebco2geneabolishesitsfunctionandleadstoyellowdiscolorationofadiposetissueinnorwegianspælsauovisaries AT arnyasimariann insertionofanendogenousjaagsiektesheepretroviruselementintothebco2geneabolishesitsfunctionandleadstoyellowdiscolorationofadiposetissueinnorwegianspælsauovisaries AT sundsaasenkristilkindem insertionofanendogenousjaagsiektesheepretroviruselementintothebco2geneabolishesitsfunctionandleadstoyellowdiscolorationofadiposetissueinnorwegianspælsauovisaries AT vagedaginge insertionofanendogenousjaagsiektesheepretroviruselementintothebco2geneabolishesitsfunctionandleadstoyellowdiscolorationofadiposetissueinnorwegianspælsauovisaries |