Evidence map›Paper›PMID 29237423›Full record

ArticleBMC genomics2017

Deciphering the genetic regulation of peripheral blood transcriptome in pigs through expression genome-wide association study and allele-specific expression analysis.

T Maroilley, G Lemonnier, J Lecardonnel, D Esquerré, Y Ramayo-Caldas, M J Mercat, C Rogel-Gaillard, J Estellé

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
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

21 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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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

8 authors at 3 institutions in 1 country.

T MaroilleyGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France. tatiana.maroilley@inra.fr.ORCID http://orcid.org/0000-0002-3392-5363
G LemonnierGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France.
J LecardonnelGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France.
D EsquerréGenPhySE, INRA, INPT, ENVT, Université de Toulouse, 31326, Castanet-Tolosan, France.
Y Ramayo-CaldasGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France.
M J MercatIFIP - Institut du porc/BIOPORC, La Motte au Vicomte, BP 35104, 35651, Le Rheu, France.
C Rogel-GaillardGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France. claire.rogel-gaillard@inra.fr.
J EstelléGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France. jordi.estelle@inra.fr.
AgroParisTech · FRÉcole Nationale Vétérinaire de Toulouse · FRInstitut du Porc · FR

Funding

Agence Nationale de la Recherche ANR-06-GANI-08Agence Nationale de la Recherche ANR-10-GENM-016BIOPORC PhD grantINRA PhD grantINRA PigMuNome
6 · The paper itself

Abstract

backgroundEfforts to improve sustainability in livestock production systems have focused on two objectives: investigating the genetic control of immune function as it pertains to robustness and disease resistance, and finding predictive markers for use in breeding programs. In this context, the peripheral blood transcriptome represents an important source of biological information about an individual's health and immunological status, and has been proposed for use as an intermediate phenotype to measure immune capacity. The objective of this work was to study the genetic architecture of variation in gene expression in the blood of healthy young pigs using two approaches: an expression genome-wide association study (eGWAS) and allele-specific expression (ASE) analysis.

resultsThe blood transcriptomes of 60-day-old Large White pigs were analyzed by expression microarrays for eGWAS (242 animals) and by RNA-Seq for ASE analysis (38 animals). Using eGWAS, the expression levels of 1901 genes were found to be associated with expression quantitative trait loci (eQTLs). We recovered 2839 local and 1752 distant associations (Single Nucleotide Polymorphism or SNP located less or more than 1 Mb from expression probe, respectively). ASE analyses confirmed the extensive cis-regulation of gene transcription in blood, and revealed allelic imbalance in 2286 SNPs, which affected 763 genes. eQTLs and ASE-genes were widely distributed on all chromosomes. By analyzing mutually overlapping eGWAS results, we were able to describe putative regulatory networks, which were further refined using ASE data. At the functional level, genes with genetically controlled expression that were detected by eGWAS and/or ASE analyses were significantly enriched in biological processes related to RNA processing and immune function. Indeed, numerous distant and local regulatory relationships were detected within the major histocompatibility complex region on chromosome 7, revealing ASE for most class I and II genes.

conclusionsThis study represents, to the best of our knowledge, the first genome-wide map of the genetic control of gene expression in porcine peripheral blood. These results represent an interesting resource for the identification of genetic markers and blood biomarkers associated with variations in immunity traits in pigs, as well as any other complex traits for which blood is an appropriate surrogate tissue.

Indexed as

AllelesTranscriptomeAnimalsBiomarkersFemaleGene Expression RegulationGene Regulatory NetworksGenome-Wide Association StudyHistocompatibility AntigensMalePolymorphism, Single NucleotideQuantitative Trait LociRNASwineBiomarkersHistocompatibility AntigensRNAAllele-Specific ExpressionBloodeGWASeQTLPigRNA-SeqTranscriptome

Identifiers

PMID29237423
PMCPMC5729405
OpenAlexW2772982121

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LicenceCC BY
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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 OpenQuestion graph.