Evidence map›Paper›PMID 27589727›Full record

ArticleInternational journal of molecular sciences2016

Integrative Analysis of Metabolomic, Proteomic and Genomic Data to Reveal Functional Pathways and Candidate Genes for Drip Loss in Pigs.

Julia Welzenbach, Christiane Neuhoff, Hanna Heidt, Mehmet Ulas Cinar, Christian Looft, Karl Schellander, Ernst Tholen, Christine Große-Brinkhaus

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

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  10. Review
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  12. Bioinformatics Methods for Mass Spectrometry-Based Proteomics Data Analysis.International journal of molecular sciences · 2020
    Review
  13. 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.

Julia WelzenbachInstitute of Animal Science, University of Bonn, Endenicher Allee 15, 53115 Bonn, Germany. jwel@itw.uni-bonn.de.
Christiane NeuhoffInstitute of Animal Science, University of Bonn, Endenicher Allee 15, 53115 Bonn, Germany. cneu@itw.uni-bonn.de.
Hanna HeidtInstitute of Animal Science, University of Bonn, Endenicher Allee 15, 53115 Bonn, Germany. heidt@ibla.lu.
Mehmet Ulas CinarInstitute of Animal Science, University of Bonn, Endenicher Allee 15, 53115 Bonn, Germany. mucinar@erciyes.edu.tr.
Christian LooftInstitute of Animal Science, University of Bonn, Endenicher Allee 15, 53115 Bonn, Germany. cloo@itw.uni-bonn.de.
Karl SchellanderInstitute of Animal Science, University of Bonn, Endenicher Allee 15, 53115 Bonn, Germany. ksch@itw.uni-bonn.de.
Ernst TholenInstitute of Animal Science, University of Bonn, Endenicher Allee 15, 53115 Bonn, Germany. etho@itw.uni-bonn.de.
Christine Große-BrinkhausInstitute of Animal Science, University of Bonn, Endenicher Allee 15, 53115 Bonn, Germany. cgro@itw.uni-bonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to integrate multi omics data to characterize underlying functional pathways and candidate genes for drip loss in pigs. The consideration of different omics levels allows elucidating the black box of phenotype expression. Metabolite and protein profiling was applied in Musculus longissimus dorsi samples of 97 Duroc × Pietrain pigs. In total, 126 and 35 annotated metabolites and proteins were quantified, respectively. In addition, all animals were genotyped with the porcine 60 k Illumina beadchip. An enrichment analysis resulted in 10 pathways, amongst others, sphingolipid metabolism and glycolysis/gluconeogenesis, with significant influence on drip loss. Drip loss and 22 metabolic components were analyzed as intermediate phenotypes within a genome-wide association study (GWAS). We detected significantly associated genetic markers and candidate genes for drip loss and for most of the metabolic components. On chromosome 18, a region with promising candidate genes was identified based on SNPs associated with drip loss, the protein "phosphoglycerate mutase 2" and the metabolite glycine. We hypothesize that association studies based on intermediate phenotypes are able to provide comprehensive insights in the genetic variation of genes directly involved in the metabolism of performance traits. In this way, the analyses contribute to identify reliable candidate genes.

Indexed as

Metabolic Networks and PathwaysMetabolomeQuantitative Trait LociAnimalsChromosomesGenome-Wide Association StudyPhenotypePolymorphism, Single NucleotideProteomeRed MeatSwineProteomecandidate genesdrip lossenrichment analysisgenome-wide association study (GWAS)metabolomicspork qualityproteomics

Identifiers

PMID27589727
PMCPMC5037705

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.