Evidence map›Paper›PMID 39905301›Full record

ArticleGenetics, selection, evolution : GSE2025

Sequence-based GWAS in 180,000 German Holstein cattle reveals new candidate variants for milk production traits.

Ana-Marija Križanac, Christian Reimer, Johannes Heise, Zengting Liu, Jennie E Pryce, Jörn Bennewitz, Georg Thaller, Clemens Falker-Gieske, Jens Tetens

Abstract read
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Article in Genetics, selection, evolution : GSE, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
–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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

9 authors.

Ana-Marija KrižanacDepartment of Animal Sciences, University of Goettingen, Burckhardtweg 2, 37077, Göttingen, Germany. ana-marija.krizanac@uni-goettingen.de.ORCID http://orcid.org/0000-0002-7446-8031
Christian ReimerCenter for Integrated Breeding Research, Department of Animal Sciences, University of Goettingen, Albrecht-Thaer-Weg 3, 37075, Göttingen, Germany.ORCID http://orcid.org/0000-0002-9697-2511
Johannes HeiseVereinigte Informationssysteme Tierhaltung w.V. (VIT), 27283, Verden, Germany.ORCID http://orcid.org/0000-0002-7605-7148
Zengting LiuVereinigte Informationssysteme Tierhaltung w.V. (VIT), 27283, Verden, Germany.ORCID http://orcid.org/0000-0002-7112-0320
Jennie E PryceAgriculture Victoria Research, AgriBio, Centre for AgriBioscience, Bundoora, VIC, 3083, Australia.ORCID http://orcid.org/0000-0002-1397-1282
Jörn BennewitzInstitute of Animal Science, University of Hohenheim, 70599, Stuttgart, Germany.ORCID http://orcid.org/0000-0001-6450-1160
Georg ThallerInstitute of Animal Breeding and Husbandry, Christian-Albrechts-University, 24118, Kiel, Germany.ORCID http://orcid.org/0000-0002-6782-2039
Clemens Falker-Gieske *Department of Animal Sciences, University of Goettingen, Burckhardtweg 2, 37077, Göttingen, Germany.ORCID http://orcid.org/0000-0001-9160-1909
Jens Tetens *Department of Animal Sciences, University of Goettingen, Burckhardtweg 2, 37077, Göttingen, Germany.ORCID http://orcid.org/0000-0001-5352-464X

Funding

Deutsche Forschungsgemeinschaft TE622/6-1
6 · The paper itself

Abstract

backgroundMilk production traits are complex and influenced by many genetic and environmental factors. Although extensive research has been performed for these traits, with many associations unveiled thus far, due to their crucial economic importance, complex genetic architecture, and the fact that causal variants in cattle are still scarce, there is a need for a better understanding of their genetic background. In this study, we aimed to identify new candidate loci associated with milk production traits in German Holstein cattle, the most important dairy breed in Germany and worldwide. For that purpose, 180,217 cattle were imputed to the sequence level and large-scale genome-wide association study (GWAS) followed by fine-mapping and evolutionary and functional annotation were carried out to identify and prioritize new association signals.

resultsUsing the imputed sequence data of a large cattle dataset, we identified 50,876 significant variants, confirming many known and identifying previously unreported candidate variants for milk (MY), fat (FY), and protein yield (PY). Genome-wide significant signals were fine-mapped with the Bayesian approach that determines the credible variant sets and generates the probability of causality for each signal. The variants with the highest probabilities of being causal were further classified using external information about the function and evolution, making the prioritization for subsequent validation experiments easier. The top potential causal variants determined with fine-mapping explained a large percentage of genetic variance compared to random ones; 178 variants explained 11.5%, 104 explained 7.7%, and 68 variants explained 3.9% of the variance for MY, FY, and PY, respectively, demonstrating the potential for causality.

conclusionsOur findings proved the power of large samples and sequence-based GWAS in detecting new association signals. In order to fully exploit the power of GWAS, one should aim at very large samples combined with whole-genome sequence data. These can also come with both computational and time burdens, as presented in our study. Although milk production traits in cattle are comprehensively investigated, the genetic background of these traits is still not fully understood, with the potential for many new associations to be revealed, as shown. With constantly growing sample sizes, we expect more insights into the genetic architecture of milk production traits in the future.

Indexed as

Genome-Wide Association StudyLactationMilkQuantitative Trait LociAnimalsBayes TheoremCattleFemaleGermanyPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID39905301
PMCPMC11796172

What Socratic holds

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Registered trials

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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 Socratic graph.