Evidence map›Paper›PMID 29272997›Full record

ArticleBMC genomics2017

Genome variation and conserved regulation identify genomic regions responsible for strain specific phenotypes in rat.

David Martín-Gálvez, Denis Dunoyer de Segonzac, Man Chun John Ma, Anne E Kwitek, David Thybert, Paul Flicek

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 78% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

David Martín-GálvezEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK.
Denis Dunoyer de SegonzacEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK.
Man Chun John MaDepartment of Pharmacology, University of Iowa, Iowa City, IA, USA.
Anne E KwitekDepartment of Pharmacology, University of Iowa, Iowa City, IA, USA.
David ThybertEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK. david.thybert@earlham.ac.uk.
Paul FlicekEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK. flicek@ebi.ac.uk.ORCID 0000-0002-3897-7955
European Bioinformatics Institute · GBUniversity of Iowa · US

Funding

Dissecting the genetics of the Metabolic Syndrome on Chromosome 17 of the LH ratR01HL089895 · NHLBI · UNIVERSITY OF IOWA · PI KWITEK, ANNE E. · 2008 to 2012
$1.7M
Identification of a metabolic syndrome transcriptome signature in the LH ratR21DK089417 · NIDDK · UNIVERSITY OF IOWA · PI KWITEK, ANNE E., XING, YI · 2010 to 2011
$411k
European Commission HEALTH-F4-2010-241504National Institutes of Health (US) R01 HL089895NHLBI NIH HHS R01 HL089895NIDDK NIH HHS R21 DK089417NIH HHS R21 DK089417Wellcome TrustWellcome Trust WT108749/Z/15/Z
6 · The paper itself

Abstract

backgroundThe genomes of laboratory rat strains are characterised by a mosaic haplotype structure caused by their unique breeding history. These mosaic haplotypes have been recently mapped by extensive sequencing of key strains. Comparison of genomic variation between two closely related rat strains with different phenotypes has been proposed as an effective strategy for the discovery of candidate strain-specific regions involved in phenotypic differences. We developed a method to prioritise strain-specific haplotypes by integrating genomic variation and genomic regulatory data predicted to be involved in specific phenotypes. Specifically, we aimed to identify genomic regions associated with Metabolic Syndrome (MetS), a disorder of energy utilization and storage affecting several organ systems.

resultsWe compared two Lyon rat strains, Lyon Hypertensive (LH) which is susceptible to MetS, and Lyon Low pressure (LL), which is susceptible to obesity as an intermediate MetS phenotype, with a third strain (Lyon Normotensive, LN) that is resistant to both MetS and obesity. Applying a novel metric, we ranked the identified strain-specific haplotypes using evolutionary conservation of the occupancy three liver-specific transcription factors (HNF4A, CEBPA, and FOXA1) in five rodents including rat. Consideration of regulatory information effectively identified regions with liver-associated genes and rat orthologues of human GWAS variants related to obesity and metabolic traits. We attempted to find possible causative variants and compared them with the candidate genes proposed by previous studies. In strain-specific regions with conserved regulation, we found a significant enrichment for published evidence to obesity-one of the metabolic symptoms shown by the Lyon strains-amongst the genes assigned to promoters with strain-specific variation.

conclusionsOur results show that the use of functional regulatory conservation is a potentially effective approach to select strain-specific genomic regions associated with phenotypic differences among Lyon rats and could be extended to other systems.

Indexed as

Genetic VariationGenomeRegulatory Elements, TranscriptionalAnimalsBase SequenceBinding SitesConserved SequenceHaplotypesHumansLiverMetabolic SyndromePhenotypeProtein Interaction MapsRatsRats, Inbred StrainsSpecies SpecificityTranscription FactorsEvolutionGenome regulationMetabolic syndrome

Identifiers

PMID29272997
PMCPMC5741965
OpenAlexW2952263075

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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.