Epigenomics and genotype-phenotype association analyses reveal conserved genetic architecture of complex traits in cattle and human.


Journal

BMC biology
ISSN: 1741-7007
Titre abrégé: BMC Biol
Pays: England
ID NLM: 101190720

Informations de publication

Date de publication:
03 07 2020
Historique:
received: 16 10 2019
accepted: 12 05 2020
entrez: 5 7 2020
pubmed: 6 7 2020
medline: 5 6 2021
Statut: epublish

Résumé

Lack of comprehensive functional annotations across a wide range of tissues and cell types severely hinders the biological interpretations of phenotypic variation, adaptive evolution, and domestication in livestock. Here we used a combination of comparative epigenomics, genome-wide association study (GWAS), and selection signature analysis, to shed light on potential adaptive evolution in cattle. We cross-mapped 8 histone marks of 1300 samples from human to cattle, covering 178 unique tissues/cell types. By uniformly analyzing 723 RNA-seq and 40 whole genome bisulfite sequencing (WGBS) datasets in cattle, we validated that cross-mapped histone marks captured tissue-specific expression and methylation, reflecting tissue-relevant biology. Through integrating cross-mapped tissue-specific histone marks with large-scale GWAS and selection signature results, we for the first time detected relevant tissues and cell types for 45 economically important traits and artificial selection in cattle. For instance, immune tissues are significantly associated with health and reproduction traits, multiple tissues for milk production and body conformation traits (reflecting their highly polygenic architecture), and thyroid for the different selection between beef and dairy cattle. Similarly, we detected relevant tissues for 58 complex traits and diseases in humans and observed that immune and fertility traits in humans significantly correlated with those in cattle in terms of relevant tissues, which facilitated the identification of causal genes for such traits. For instance, PIK3CG, a gene highly specifically expressed in mononuclear cells, was significantly associated with both age-at-menopause in human and daughter-still-birth in cattle. ICAM, a T cell-specific gene, was significantly associated with both allergic diseases in human and metritis in cattle. Collectively, our results highlighted that comparative epigenomics in conjunction with GWAS and selection signature analyses could provide biological insights into the phenotypic variation and adaptive evolution. Cattle may serve as a model for human complex traits, by providing additional information beyond laboratory model organisms, particularly when more novel phenotypes become available in the near future.

Sections du résumé

BACKGROUND
Lack of comprehensive functional annotations across a wide range of tissues and cell types severely hinders the biological interpretations of phenotypic variation, adaptive evolution, and domestication in livestock. Here we used a combination of comparative epigenomics, genome-wide association study (GWAS), and selection signature analysis, to shed light on potential adaptive evolution in cattle.
RESULTS
We cross-mapped 8 histone marks of 1300 samples from human to cattle, covering 178 unique tissues/cell types. By uniformly analyzing 723 RNA-seq and 40 whole genome bisulfite sequencing (WGBS) datasets in cattle, we validated that cross-mapped histone marks captured tissue-specific expression and methylation, reflecting tissue-relevant biology. Through integrating cross-mapped tissue-specific histone marks with large-scale GWAS and selection signature results, we for the first time detected relevant tissues and cell types for 45 economically important traits and artificial selection in cattle. For instance, immune tissues are significantly associated with health and reproduction traits, multiple tissues for milk production and body conformation traits (reflecting their highly polygenic architecture), and thyroid for the different selection between beef and dairy cattle. Similarly, we detected relevant tissues for 58 complex traits and diseases in humans and observed that immune and fertility traits in humans significantly correlated with those in cattle in terms of relevant tissues, which facilitated the identification of causal genes for such traits. For instance, PIK3CG, a gene highly specifically expressed in mononuclear cells, was significantly associated with both age-at-menopause in human and daughter-still-birth in cattle. ICAM, a T cell-specific gene, was significantly associated with both allergic diseases in human and metritis in cattle.
CONCLUSION
Collectively, our results highlighted that comparative epigenomics in conjunction with GWAS and selection signature analyses could provide biological insights into the phenotypic variation and adaptive evolution. Cattle may serve as a model for human complex traits, by providing additional information beyond laboratory model organisms, particularly when more novel phenotypes become available in the near future.

Identifiants

pubmed: 32620158
doi: 10.1186/s12915-020-00792-6
pii: 10.1186/s12915-020-00792-6
pmc: PMC7334855
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

80

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/D/30002275
Pays : United Kingdom
Organisme : HDR-UK
ID : HDR-9004
Pays : International
Organisme : NHGRI NIH HHS
ID : U41 HG010972
Pays : United States
Organisme : NHGRI NIH HHS
ID : R01 HG007175
Pays : United States
Organisme : National Institute of Food and Agriculture
ID : 2013-67015-20951
Pays : International
Organisme : H2020 Marie Skłodowska-Curie Actions
ID : 801215
Pays : International
Organisme : NCI NIH HHS
ID : U01 CA200060
Pays : United States
Organisme : National Institute of Food and Agriculture
ID : 2016-67015-24886
Pays : International
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/D/10002070
Pays : United Kingdom
Organisme : NIDA NIH HHS
ID : R25 DA027995
Pays : United States
Organisme : National Institute of Food and Agriculture
ID : 2019-67015-29321
Pays : International
Organisme : MRF
ID : MR/P015514/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P015514/1
Pays : United Kingdom
Organisme : United States - Israel Binational Agricultural Research and Development Fund
ID : US-4997-17
Pays : International
Organisme : NIEHS NIH HHS
ID : U24 ES026699
Pays : United States

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Auteurs

Shuli Liu (S)

Animal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, BARC-East, Beltsville, MD, 20705, USA.
College of Animal Science and Technology, China Agricultural University, Beijing, 100193, China.

Ying Yu (Y)

College of Animal Science and Technology, China Agricultural University, Beijing, 100193, China.

Shengli Zhang (S)

College of Animal Science and Technology, China Agricultural University, Beijing, 100193, China.

John B Cole (JB)

Animal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, BARC-East, Beltsville, MD, 20705, USA.

Albert Tenesa (A)

MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.
The Roslin Institute, University of Edinburgh, Edinburgh, EH25 9RG, UK.

Ting Wang (T)

Department of Genetics, Washington University School of Medicine, St. Louis, MO, 63110, USA.

Tara G McDaneld (TG)

US Meat Animal Research Center, Agricultural Research Service, USDA, Clay Center, NE, 68933, USA.

Li Ma (L)

Department of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA. lima@umd.edu.

George E Liu (GE)

Animal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, BARC-East, Beltsville, MD, 20705, USA. George.Liu@usda.gov.

Lingzhao Fang (L)

Animal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, BARC-East, Beltsville, MD, 20705, USA. Lingzhao.fang@igmm.ed.ac.uk.
MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK. Lingzhao.fang@igmm.ed.ac.uk.
Department of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA. Lingzhao.fang@igmm.ed.ac.uk.

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