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SLA-1 Genetic Diversity in Pigs: Extensive Analysis of Copy Number Variation, Heterozygosity, Expression, and Breed Specificity
Swine leukocyte antigens play indispensable roles in immune responses by recognizing a large number of foreign antigens and thus, their genetic diversity plays a critical role in their functions. In this study, we developed a new high-resolution typing method for pig SLA-1 and successfully typed 307...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971002/ https://www.ncbi.nlm.nih.gov/pubmed/31959823 http://dx.doi.org/10.1038/s41598-020-57712-5 |
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author | Le, Minh Thong Choi, Hojun Lee, Hyejeong Le, Van Chanh Quy Ahn, Byeongyong Ho, Chak-Sum Hong, Kwonho Song, Hyuk Kim, Jin-Hoi Park, Chankyu |
author_facet | Le, Minh Thong Choi, Hojun Lee, Hyejeong Le, Van Chanh Quy Ahn, Byeongyong Ho, Chak-Sum Hong, Kwonho Song, Hyuk Kim, Jin-Hoi Park, Chankyu |
author_sort | Le, Minh Thong |
collection | PubMed |
description | Swine leukocyte antigens play indispensable roles in immune responses by recognizing a large number of foreign antigens and thus, their genetic diversity plays a critical role in their functions. In this study, we developed a new high-resolution typing method for pig SLA-1 and successfully typed 307 individuals from diverse genetic backgrounds including 11 pure breeds, 1 cross bred, and 12 cell lines. We identified a total of 52 alleles including 18 novel alleles and 9 SLA-1 duplication haplotypes, including 4 new haplotypes. We observed significant differences in the distribution of SLA-1 alleles among the different pig breeds, including the breed specific alleles. SLA-1 duplication was observed in 33% of the chromosomes and was especially high in the biomedical model breeds such as SNU (100%) and NIH (76%) miniature pigs. Our analysis showed that SLA-1 duplication is associated with the increased level of SLA-1 mRNA expression in porcine cells compared to that of the single copy haplotype. Therefore, we provide here the results of the most extensive genetic analysis on pig SLA-1. |
format | Online Article Text |
id | pubmed-6971002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69710022020-01-27 SLA-1 Genetic Diversity in Pigs: Extensive Analysis of Copy Number Variation, Heterozygosity, Expression, and Breed Specificity Le, Minh Thong Choi, Hojun Lee, Hyejeong Le, Van Chanh Quy Ahn, Byeongyong Ho, Chak-Sum Hong, Kwonho Song, Hyuk Kim, Jin-Hoi Park, Chankyu Sci Rep Article Swine leukocyte antigens play indispensable roles in immune responses by recognizing a large number of foreign antigens and thus, their genetic diversity plays a critical role in their functions. In this study, we developed a new high-resolution typing method for pig SLA-1 and successfully typed 307 individuals from diverse genetic backgrounds including 11 pure breeds, 1 cross bred, and 12 cell lines. We identified a total of 52 alleles including 18 novel alleles and 9 SLA-1 duplication haplotypes, including 4 new haplotypes. We observed significant differences in the distribution of SLA-1 alleles among the different pig breeds, including the breed specific alleles. SLA-1 duplication was observed in 33% of the chromosomes and was especially high in the biomedical model breeds such as SNU (100%) and NIH (76%) miniature pigs. Our analysis showed that SLA-1 duplication is associated with the increased level of SLA-1 mRNA expression in porcine cells compared to that of the single copy haplotype. Therefore, we provide here the results of the most extensive genetic analysis on pig SLA-1. Nature Publishing Group UK 2020-01-20 /pmc/articles/PMC6971002/ /pubmed/31959823 http://dx.doi.org/10.1038/s41598-020-57712-5 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 Le, Minh Thong Choi, Hojun Lee, Hyejeong Le, Van Chanh Quy Ahn, Byeongyong Ho, Chak-Sum Hong, Kwonho Song, Hyuk Kim, Jin-Hoi Park, Chankyu SLA-1 Genetic Diversity in Pigs: Extensive Analysis of Copy Number Variation, Heterozygosity, Expression, and Breed Specificity |
title | SLA-1 Genetic Diversity in Pigs: Extensive Analysis of Copy Number Variation, Heterozygosity, Expression, and Breed Specificity |
title_full | SLA-1 Genetic Diversity in Pigs: Extensive Analysis of Copy Number Variation, Heterozygosity, Expression, and Breed Specificity |
title_fullStr | SLA-1 Genetic Diversity in Pigs: Extensive Analysis of Copy Number Variation, Heterozygosity, Expression, and Breed Specificity |
title_full_unstemmed | SLA-1 Genetic Diversity in Pigs: Extensive Analysis of Copy Number Variation, Heterozygosity, Expression, and Breed Specificity |
title_short | SLA-1 Genetic Diversity in Pigs: Extensive Analysis of Copy Number Variation, Heterozygosity, Expression, and Breed Specificity |
title_sort | sla-1 genetic diversity in pigs: extensive analysis of copy number variation, heterozygosity, expression, and breed specificity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971002/ https://www.ncbi.nlm.nih.gov/pubmed/31959823 http://dx.doi.org/10.1038/s41598-020-57712-5 |
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