Preprint · not peer-reviewed Researchers Educators

Genome-wide meQTL mapping in cattle blood identifies cis and trans regulators of DNA methylation

A bioRxiv preprint uses the bovine EpiChip methylation array to map methylation quantitative trait loci across the cattle genome, opening new avenues for dissecting complex trait regulation in livestock.

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A preprint posted to bioRxiv reports the first large-scale methylation quantitative trait locus (meQTL) mapping study in cattle, using a recently developed epigenotyping array called EpiChip. Developed as part of the European RUMIGEN project, EpiChip interrogates 43,317 CpG sites distributed across the bovine genome. The authors applied this resource to blood samples, identifying both cis-acting meQTLs — where a genetic variant influences methylation at a nearby genomic position — and trans-acting meQTLs, where a variant influences methylation at a more distant locus.

MeQTL mapping is of interest in livestock genetics because DNA methylation represents one mechanism through which genetic variation can influence gene expression and ultimately phenotypic traits such as milk production, disease resistance, and growth. The identification of trans-acting meQTLs is particularly informative for understanding how individual genetic variants may propagate regulatory effects across the genome.

The study contributes to a broader effort to build multi-omic reference resources for cattle, analogous to projects such as GTEx in humans, which map how genetic variation shapes molecular phenotypes. The EpiChip array's relatively compact size compared with whole-genome bisulphite sequencing makes large-scale population studies of this kind tractable. The preprint has not yet been peer-reviewed.

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  1. Primary sourcePreprint bioRxiv (Cold Spring Harbor Laboratory) · 2026-07-08
    Genome-wide meQTL mapping in cattle blood reveals cis and trans regulation of DNA methylation

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meqtl dna-methylation cattle livestock-genomics epichip epigenetics rumigen quantitative-genetics
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Genetic Current is the news section of Evagene, an academic, research, and educational pedigree-modelling platform. Stories are AI-drafted summaries of items from trusted public sources, written for researchers, clinicians, educators, students, genealogists, and patients with an interest in genetics. Summaries are for educational and research purposes only and are not medical advice.

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