Evidence map›Paper›PMID 31931710›Full record

ArticleBMC genomics2020

GWAS and fine-mapping of livability and six disease traits in Holstein cattle.

Ellen Freebern, Daniel J A Santos, Lingzhao Fang, Jicai Jiang, Kristen L Parker Gaddis, George E Liu, Paul M VanRaden, Christian Maltecca, John B Cole, Li Ma

Abstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

71 citing papers in PubMed.

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11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Ellen FreebernDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA.
Daniel J A SantosDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA.
Lingzhao FangDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA.
Jicai JiangDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA.
Kristen L Parker GaddisCouncil on Dairy Cattle Breeding, Bowie, MD, 20716, USA.
George E LiuAnimal Genomics and Improvement Laboratory, Henry A. Wallace Beltsville Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
Paul M VanRadenAnimal Genomics and Improvement Laboratory, Henry A. Wallace Beltsville Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
Christian MalteccaDepartment of Animal Science, North Carolina State University, Raleigh, 27695, USA.
John B ColeAnimal Genomics and Improvement Laboratory, Henry A. Wallace Beltsville Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
Li MaDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA. lima@umd.edu.ORCID http://orcid.org/0000-0003-1038-1081

Funding

National Institute of Food and Agriculture 2016-67015-24886National Institute of Food and Agriculture 2018-67015-28128United States - Israel Binational Agricultural Research and Development Fund US-4997-17
6 · The paper itself

Abstract

backgroundHealth traits are of significant economic importance to the dairy industry due to their effects on milk production and associated treatment costs. Genome-wide association studies (GWAS) provide a means to identify associated genomic variants and thus reveal insights into the genetic architecture of complex traits and diseases. The objective of this study is to investigate the genetic basis of seven health traits in dairy cattle and to identify potential candidate genes associated with cattle health using GWAS, fine mapping, and analyses of multi-tissue transcriptome data.

resultsWe studied cow livability and six direct disease traits, mastitis, ketosis, hypocalcemia, displaced abomasum, metritis, and retained placenta, using de-regressed breeding values and more than three million imputed DNA sequence variants. After data edits and filtering on reliability, the number of bulls included in the analyses ranged from 11,880 (hypocalcemia) to 24,699 (livability). GWAS was performed using a mixed-model association test, and a Bayesian fine-mapping procedure was conducted to calculate a posterior probability of causality to each variant and gene in the candidate regions. The GWAS detected a total of eight genome-wide significant associations for three traits, cow livability, ketosis, and hypocalcemia, including the bovine Major Histocompatibility Complex (MHC) region associated with livability. Our fine-mapping of associated regions reported 20 candidate genes with the highest posterior probabilities of causality for cattle health. Combined with transcriptome data across multiple tissues in cattle, we further exploited these candidate genes to identify specific expression patterns in disease-related tissues and relevant biological explanations such as the expression of Group-specific Component (GC) in the liver and association with mastitis as well as the Coiled-Coil Domain Containing 88C (CCDC88C) expression in CD8 cells and association with cow livability.

conclusionsCollectively, our analyses report six significant associations and 20 candidate genes of cattle health. With the integration of multi-tissue transcriptome data, our results provide useful information for future functional studies and better understanding of the biological relationship between genetics and disease susceptibility in cattle.

Indexed as

Chromosome MappingGenome-Wide Association StudyQuantitative Trait, HeritableQuantitative Trait LociAnimalsCattleCattle DiseasesDairyingGenetic Predisposition to DiseaseGenomicsPhenotypePolymorphism, Single NucleotideTranscriptomeDairy cattleFine mappingGene expressionGWASHealth trait

Identifiers

PMID31931710
PMCPMC6958677

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.