ArticleGenetics, selection, evolution : GSE2026
Genomic analysis of the inbreeding load for body weight, carcass and reproductive traits in the Rubia Gallega beef cattle population.
Article in Genetics, selection, evolution : GSE, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
backgroundInbreeding, resulting from mating between relatives, leads to inbreeding depression, which can be traced back to hidden ancestral inbreeding loads. These loads exhibit variability and act as additive genetic effects that are only expressed in the inbred offspring. The objective of this study was to quantify the variance of the inbreeding loads and its correlation with additive genetic effects for seven traits in the Rubia Gallega population: birth weight, weaning weight, cold carcass weight, carcass conformation, carcass fatness, calving interval, and age at first parity. A single-step GBLUP Bayesian analysis was used by a Gibbs sampler. Additionally, the equivalence between GBLUP and SNP-BLUP was used for locating the genomic regions associated with the highest variances.
resultsThe pedigree included 522,885 animals, of which 4984 were genotyped with the Axiom_BovMDv3 chip. A total of 246,393 individuals were inbred, with an average inbreeding coefficient of 0.044 ± 0.059, attributed to 4712 ancestors through 9.8 million partial inbreeding contributions. The estimated proportion of phenotypic variance explained by inbreeding loads for an inbreeding coefficient of 0.10 ranged from 0.012 (Birth weight) to 0.101 (Weaning weight), consistently below the heritabilities of the traits. Genetic correlations between inbreeding load and additive effects were always negative. The average prediction accuracy for inbreeding-load effects in young selection candidates was low and exceeded 0.7 only in older animals. The genomic distribution of additive and inbreeding load variances was uneven, with some regions overlapping and others being specific to inbreeding load.
conclusionsThis study demonstrates that the inbreeding load variance is low compared to the additive genetic variance across a range of growth, carcass, and reproductive traits. The results were also consistent with a previous study that theoretically demonstrated a negative correlation between additive effects and inbreeding load. The potential to purge deleterious alleles appears limited, largely due to the low prediction accuracy observed in young individuals. Nevertheless, the higher accuracy of inbreeding-load estimates in ancestral animals could still be exploited to guide the unavoidable inbreeding in small populations through informed mating strategies, thereby minimizing undesirable inbreeding-depression effects. The heterogeneous genomic distribution of the inbreeding load suggests new opportunities for identifying genes in which deleterious or semideleterious alleles may be located.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.