Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/34599
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dc.contributor.authorFreem, Lucyen_UK
dc.contributor.authorSummers, Kim Men_UK
dc.contributor.authorGheyas, Almas Aen_UK
dc.contributor.authorPsifidi, Andronikien_UK
dc.contributor.authorBoulton, Kayen_UK
dc.contributor.authorMacCallum, Amandaen_UK
dc.contributor.authorHarne, Rakhien_UK
dc.contributor.authorO’Dell, Jennyen_UK
dc.contributor.authorBush, Stephen Jen_UK
dc.contributor.authorHume, David Aen_UK
dc.date.accessioned2022-10-16T00:00:40Z-
dc.date.available2022-10-16T00:00:40Z-
dc.date.issued2019en_UK
dc.identifier.other1032en_UK
dc.identifier.urihttp://hdl.handle.net/1893/34599-
dc.description.abstractThere is increasing recognition that the underlying genetic variation contributing to complex traits influences transcriptional regulation and can be detected at a population level as expression quantitative trait loci. At the level of an individual, allelic variation in transcriptional regulation of individual genes can be detected by measuring allele-specific expression in RNAseq data. We reasoned that extreme variants in gene expression could be identified by analysis of inbred progeny with shared grandparents. Commercial chickens have been intensively selected for production traits. Selection is associated with large blocks of linkage disequilibrium with considerable potential for co-selection of closely linked “hitch-hiker alleles” affecting traits unrelated to the feature being selected, such as immune function, with potential impact on the productivity and welfare of the animals. To test this hypothesis that there is extreme allelic variation in immune-associated genes we sequenced a founder population of commercial broiler and layer birds. These birds clearly segregated genetically based upon breed type. Each genome contained numerous candidate null mutations, protein-coding variants predicted to be deleterious and extensive non-coding polymorphism. We mated selected broiler-layer pairs then generated cohorts of F2 birds by sibling mating of the F1 generation. Despite the predicted prevalence of deleterious coding variation in the genomic sequence of the founders, clear detrimental impacts of inbreeding on survival and post-hatch development were detected in only one F2 sibship of 15. There was no effect on circulating leukocyte populations in hatchlings. In selected F2 sibships we performed RNAseq analysis of the spleen and isolated bone marrow-derived macrophages (with and without lipopolysaccharide stimulation). The results confirm the predicted emergence of very large differences in expression of individual genes and sets of genes. Network analysis of the results identified clusters of co-expressed genes that vary between individuals and suggested the existence of trans-acting variation in the expression in macrophages of the interferon response factor family that distinguishes the parental broiler and layer birds and influences the global response to lipopolysaccharide. This study shows that the impact of inbreeding on immune cell gene expression can be substantial at the transcriptional level, and potentially opens a route to accelerate selection using specific alleles known to be associated with desirable expression levels.en_UK
dc.language.isoenen_UK
dc.publisherFrontiers Media SAen_UK
dc.relationFreem L, Summers KM, Gheyas AA, Psifidi A, Boulton K, MacCallum A, Harne R, O’Dell J, Bush SJ & Hume DA (2019) Analysis of the Progeny of Sibling Matings Reveals Regulatory Variation Impacting the Transcriptome of Immune Cells in Commercial Chickens. Frontiers in Genetics, 10, Art. No.: 1032. https://doi.org/10.3389/fgene.2019.01032en_UK
dc.rights© 2019 Freem, Summers, Gheyas, Psifidi, Boulton, MacCallum, Harne, O’Dell, Bush and Hume. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY - https://creativecommons.org/licenses/by/4.0/). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectchickenen_UK
dc.subjectgenomeen_UK
dc.subjectinbreedingen_UK
dc.subjectallele-specificen_UK
dc.subjecttranscriptomeen_UK
dc.subjectmacrophageen_UK
dc.titleAnalysis of the Progeny of Sibling Matings Reveals Regulatory Variation Impacting the Transcriptome of Immune Cells in Commercial Chickensen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.3389/fgene.2019.01032en_UK
dc.identifier.pmid31803225en_UK
dc.citation.jtitleFrontiers in Geneticsen_UK
dc.citation.issn1664-8021en_UK
dc.citation.volume10en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderBiotechnology and Biological Sciences Research Councilen_UK
dc.contributor.funderBiotechnology and Biological Sciences Research Councilen_UK
dc.contributor.funderBiotechnology and Biological Sciences Research Councilen_UK
dc.author.emailalmas.gheyas@stir.ac.uken_UK
dc.citation.date14/11/2019en_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Queenslanden_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Londonen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Oxforden_UK
dc.contributor.affiliationUniversity of Queenslanden_UK
dc.identifier.isiWOS:000587355500001en_UK
dc.identifier.scopusid2-s2.0-85075980935en_UK
dc.identifier.wtid1831145en_UK
dc.contributor.orcid0000-0002-7682-4394en_UK
dc.date.accepted2019-09-25en_UK
dcterms.dateAccepted2019-09-25en_UK
dc.date.filedepositdate2022-10-15en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorFreem, Lucy|en_UK
local.rioxx.authorSummers, Kim M|en_UK
local.rioxx.authorGheyas, Almas A|0000-0002-7682-4394en_UK
local.rioxx.authorPsifidi, Androniki|en_UK
local.rioxx.authorBoulton, Kay|en_UK
local.rioxx.authorMacCallum, Amanda|en_UK
local.rioxx.authorHarne, Rakhi|en_UK
local.rioxx.authorO’Dell, Jenny|en_UK
local.rioxx.authorBush, Stephen J|en_UK
local.rioxx.authorHume, David A|en_UK
local.rioxx.projectBBS/E/D/20211552|Biotechnology and Biological Sciences Research Council|http://dx.doi.org/10.13039/501100000268en_UK
local.rioxx.projectBBS/E/D/20211550|Biotechnology and Biological Sciences Research Council|http://dx.doi.org/10.13039/501100000268en_UK
local.rioxx.projectBB/M011925/1|Biotechnology and Biological Sciences Research Council|http://dx.doi.org/10.13039/501100000268en_UK
local.rioxx.freetoreaddate2022-10-15en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2022-10-15|en_UK
local.rioxx.filenamefgene-10-01032.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1664-8021en_UK
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