Cargando…
Pig genome functional annotation enhances the biological interpretation of complex traits and human disease
The functional annotation of livestock genomes is crucial for understanding the molecular mechanisms that underpin complex traits of economic importance, adaptive evolution and comparative genomics. Here, we provide the most comprehensive catalogue to date of regulatory elements in the pig (Sus scro...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494738/ https://www.ncbi.nlm.nih.gov/pubmed/34615879 http://dx.doi.org/10.1038/s41467-021-26153-7 |
_version_ | 1784579379972538368 |
---|---|
author | Pan, Zhangyuan Yao, Yuelin Yin, Hongwei Cai, Zexi Wang, Ying Bai, Lijing Kern, Colin Halstead, Michelle Chanthavixay, Ganrea Trakooljul, Nares Wimmers, Klaus Sahana, Goutam Su, Guosheng Lund, Mogens Sandø Fredholm, Merete Karlskov-Mortensen, Peter Ernst, Catherine W. Ross, Pablo Tuggle, Christopher K. Fang, Lingzhao Zhou, Huaijun |
author_facet | Pan, Zhangyuan Yao, Yuelin Yin, Hongwei Cai, Zexi Wang, Ying Bai, Lijing Kern, Colin Halstead, Michelle Chanthavixay, Ganrea Trakooljul, Nares Wimmers, Klaus Sahana, Goutam Su, Guosheng Lund, Mogens Sandø Fredholm, Merete Karlskov-Mortensen, Peter Ernst, Catherine W. Ross, Pablo Tuggle, Christopher K. Fang, Lingzhao Zhou, Huaijun |
author_sort | Pan, Zhangyuan |
collection | PubMed |
description | The functional annotation of livestock genomes is crucial for understanding the molecular mechanisms that underpin complex traits of economic importance, adaptive evolution and comparative genomics. Here, we provide the most comprehensive catalogue to date of regulatory elements in the pig (Sus scrofa) by integrating 223 epigenomic and transcriptomic data sets, representing 14 biologically important tissues. We systematically describe the dynamic epigenetic landscape across tissues by functionally annotating 15 different chromatin states and defining their tissue-specific regulatory activities. We demonstrate that genomic variants associated with complex traits and adaptive evolution in pig are significantly enriched in active promoters and enhancers. Furthermore, we reveal distinct tissue-specific regulatory selection between Asian and European pig domestication processes. Compared with human and mouse epigenomes, we show that porcine regulatory elements are more conserved in DNA sequence, under both rapid and slow evolution, than those under neutral evolution across pig, mouse, and human. Finally, we provide biological insights on tissue-specific regulatory conservation, and by integrating 47 human genome-wide association studies, we demonstrate that, depending on the traits, mouse or pig might be more appropriate biomedical models for different complex traits and diseases. |
format | Online Article Text |
id | pubmed-8494738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84947382021-10-07 Pig genome functional annotation enhances the biological interpretation of complex traits and human disease Pan, Zhangyuan Yao, Yuelin Yin, Hongwei Cai, Zexi Wang, Ying Bai, Lijing Kern, Colin Halstead, Michelle Chanthavixay, Ganrea Trakooljul, Nares Wimmers, Klaus Sahana, Goutam Su, Guosheng Lund, Mogens Sandø Fredholm, Merete Karlskov-Mortensen, Peter Ernst, Catherine W. Ross, Pablo Tuggle, Christopher K. Fang, Lingzhao Zhou, Huaijun Nat Commun Article The functional annotation of livestock genomes is crucial for understanding the molecular mechanisms that underpin complex traits of economic importance, adaptive evolution and comparative genomics. Here, we provide the most comprehensive catalogue to date of regulatory elements in the pig (Sus scrofa) by integrating 223 epigenomic and transcriptomic data sets, representing 14 biologically important tissues. We systematically describe the dynamic epigenetic landscape across tissues by functionally annotating 15 different chromatin states and defining their tissue-specific regulatory activities. We demonstrate that genomic variants associated with complex traits and adaptive evolution in pig are significantly enriched in active promoters and enhancers. Furthermore, we reveal distinct tissue-specific regulatory selection between Asian and European pig domestication processes. Compared with human and mouse epigenomes, we show that porcine regulatory elements are more conserved in DNA sequence, under both rapid and slow evolution, than those under neutral evolution across pig, mouse, and human. Finally, we provide biological insights on tissue-specific regulatory conservation, and by integrating 47 human genome-wide association studies, we demonstrate that, depending on the traits, mouse or pig might be more appropriate biomedical models for different complex traits and diseases. Nature Publishing Group UK 2021-10-06 /pmc/articles/PMC8494738/ /pubmed/34615879 http://dx.doi.org/10.1038/s41467-021-26153-7 Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Pan, Zhangyuan Yao, Yuelin Yin, Hongwei Cai, Zexi Wang, Ying Bai, Lijing Kern, Colin Halstead, Michelle Chanthavixay, Ganrea Trakooljul, Nares Wimmers, Klaus Sahana, Goutam Su, Guosheng Lund, Mogens Sandø Fredholm, Merete Karlskov-Mortensen, Peter Ernst, Catherine W. Ross, Pablo Tuggle, Christopher K. Fang, Lingzhao Zhou, Huaijun Pig genome functional annotation enhances the biological interpretation of complex traits and human disease |
title | Pig genome functional annotation enhances the biological interpretation of complex traits and human disease |
title_full | Pig genome functional annotation enhances the biological interpretation of complex traits and human disease |
title_fullStr | Pig genome functional annotation enhances the biological interpretation of complex traits and human disease |
title_full_unstemmed | Pig genome functional annotation enhances the biological interpretation of complex traits and human disease |
title_short | Pig genome functional annotation enhances the biological interpretation of complex traits and human disease |
title_sort | pig genome functional annotation enhances the biological interpretation of complex traits and human disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494738/ https://www.ncbi.nlm.nih.gov/pubmed/34615879 http://dx.doi.org/10.1038/s41467-021-26153-7 |
work_keys_str_mv | AT panzhangyuan piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT yaoyuelin piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT yinhongwei piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT caizexi piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT wangying piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT bailijing piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT kerncolin piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT halsteadmichelle piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT chanthavixayganrea piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT trakooljulnares piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT wimmersklaus piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT sahanagoutam piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT suguosheng piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT lundmogenssandø piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT fredholmmerete piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT karlskovmortensenpeter piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT ernstcatherinew piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT rosspablo piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT tugglechristopherk piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT fanglingzhao piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease AT zhouhuaijun piggenomefunctionalannotationenhancesthebiologicalinterpretationofcomplextraitsandhumandisease |