Evidence map›Paper›PMID 25226791›Full record

ArticleBMC genomics2014

Muscle transcriptomic investigation of late fetal development identifies candidate genes for piglet maturity.

Valentin Voillet, Magali SanCristobal, Yannick Lippi, Pascal G P Martin, Nathalie Iannuccelli, Christine Lascor, Florence Vignoles, Yvon Billon, Laurianne Canario, Laurence Liaubet

Abstract read
In one paragraph

Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

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  7. PlasmaScientific reports · 2023
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4 · The record

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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

10 authors.

Valentin Voillet
Magali SanCristobal
Yannick Lippi
Pascal G P Martin
Nathalie Iannuccelli
Christine Lascor
Florence Vignoles
Yvon Billon
Laurianne Canario
Laurence LiaubetINRA, UMR1388 Génétique, Physiologie et Systèmes d' Elevage, F-31326 Castanet-Tolosan, France. laurence.liaubet@toulouse.inra.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn pigs, the perinatal period is the most critical time for survival. Piglet maturation, which occurs at the end of gestation, leads to a state of full development after birth. Therefore, maturity is an important determinant of early survival. Skeletal muscle plays a key role in adaptation to extra-uterine life, e.g. glycogen storage and thermoregulation. In this study, we performed microarray analysis to identify the genes and biological processes involved in piglet muscle maturity. Progeny from two breeds with extreme muscle maturity phenotypes were analyzed at two time points during gestation (gestational days 90 and 110). The Large White (LW) breed is a selected breed with an increased rate of mortality at birth, whereas the Meishan (MS) breed produces piglets with extremely low mortality at birth. The impact of the parental genome was analyzed with reciprocal crossed fetuses.

resultsMicroarray analysis identified 12,326 differentially expressed probes for gestational age and genotype. Such a high number reflects an important transcriptomic change that occurs between 90 and 110 days of gestation. 2,000 probes, corresponding to 1,120 unique annotated genes, involved more particularly in the maturation process were further studied. Functional enrichment and graph inference studies underlined genes involved in muscular development around 90 days of gestation, and genes involved in metabolic functions, such as gluconeogenesis, around 110 days of gestation. Moreover, a difference in the expression of key genes, e.g. PCK2, LDHA or PGK1, was detected between MS and LW just before birth. Reciprocal crossing analysis resulted in the identification of 472 genes with an expression preferentially regulated by one parental genome. Most of these genes (366) were regulated by the paternal genome. Among these paternally regulated genes, some known imprinted genes, such as MAGEL2 or IGF2, were identified and could have a key role in the maturation process.

conclusionThese results reveal the biological mechanisms that regulate muscle maturity in piglets. Maturity is also under the conflicting regulation of the parental genomes. Crucial genes, which could explain the biological differences in maturity observed between LW and MS breeds, were identified. These genes could be excellent candidates for a key role in the maturity.

Indexed as

Gene Expression Regulation, DevelopmentalGenetic Association StudiesAnimalsBreedingFemaleFetal DevelopmentGene Expression ProfilingGene OntologyGene Regulatory NetworksGenomeGenotypeMuscle DevelopmentMuscle, SkeletalOligonucleotide Array Sequence AnalysisPregnancyPrincipal Component Analysis

Identifiers

PMID25226791
PMCPMC4287105

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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.