Evidence map›Paper›PMID 26842494›Full record

ArticleGenetics, selection, evolution : GSE2016

Differential contribution of genomic regions to marked genetic variation and prediction of quantitative traits in broiler chickens.

Rostam Abdollahi-Arpanahi, Gota Morota, Bruno D Valente, Andreas Kranis, Guilherme J M Rosa, Daniel Gianola

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Article in Genetics, selection, evolution : GSE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

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18citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rostam Abdollahi-ArpanahiDepartment of Animal Sciences, University of Wisconsin, Madison, WI, USA. r.abdollahi@ut.ac.ir.
Gota MorotaDepartment of Animal Science, University of Nebraska, Lincoln, NE, USA. morota@unl.edu.
Bruno D ValenteDepartment of Animal Sciences, University of Wisconsin, Madison, WI, USA. bvalente@wisc.edu.
Andreas KranisAviagen Ltd, Midlothian, UK. akranis@aviagen.com.
Guilherme J M RosaDepartment of Animal Sciences, University of Wisconsin, Madison, WI, USA. grosa@wisc.edu.
Daniel GianolaDepartment of Animal Sciences, University of Wisconsin, Madison, WI, USA. gianola@ansci.wisc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenome-wide association studies in humans have found enrichment of trait-associated single nucleotide polymorphisms (SNPs) in coding regions of the genome and depletion of these in intergenic regions. However, a recent release of the ENCyclopedia of DNA elements showed that ~80 % of the human genome has a biochemical function. Similar studies on the chicken genome are lacking, thus assessing the relative contribution of its genic and non-genic regions to variation is relevant for biological studies and genetic improvement of chicken populations.

methodsA dataset including 1351 birds that were genotyped with the 600K Affymetrix platform was used. We partitioned SNPs according to genome annotation data into six classes to characterize the relative contribution of genic and non-genic regions to genetic variation as well as their predictive power using all available quality-filtered SNPs. Target traits were body weight, ultrasound measurement of breast muscle and hen house egg production in broiler chickens. Six genomic regions were considered: intergenic regions, introns, missense, synonymous, 5' and 3' untranslated regions, and regions that are located 5 kb upstream and downstream of coding genes. Genomic relationship matrices were constructed for each genomic region and fitted in the models, separately or simultaneously. Kernel-based ridge regression was used to estimate variance components and assess predictive ability. Contribution of each class of genomic regions to dominance variance was also considered.

resultsVariance component estimates indicated that all genomic regions contributed to marked additive genetic variation and that the class of synonymous regions tended to have the greatest contribution. The marked dominance genetic variation explained by each class of genomic regions was similar and negligible (~0.05). In terms of prediction mean-square error, the whole-genome approach showed the best predictive ability.

conclusionsAll genic and non-genic regions contributed to phenotypic variation for the three traits studied. Overall, the contribution of additive genetic variance to the total genetic variance was much greater than that of dominance variance. Our results show that all genomic regions are important for the prediction of the targeted traits, and the whole-genome approach was reaffirmed as the best tool for genome-enabled prediction of quantitative traits.

Indexed as

GenomePolymorphism, Single NucleotideQuantitative Trait LociAnimalsBody WeightChickensDatasets as TopicEggsFemaleGenomicsGenotypeMeatPhenotypeSelection, Genetic

Identifiers

PMID26842494
PMCPMC4739338

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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 OpenQuestion graph.