Evidence map›Paper›PMID 24551844›Full record

ArticleBioMed research international2014

Differential gene expression in high- and low-active inbred mice.

Michelle Dawes, Trudy Moore-Harrison, Alicia T Hamilton, Tyrone Ceaser, Kelli J Kochan, Penny K Riggs, J Timothy Lightfoot

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 11 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

7 authors at 2 institutions in 1 country.

Michelle DawesDepartment of Health and Kinesiology, Texas A&M University, College Station, TX 77843, USA ; Sydney and JL Huffines Institute for Sports Medicine and Human Performance, Texas A&M University, College Station, TX 77843, USA.
Trudy Moore-HarrisonDepartment of Kinesiology, University of North Carolina Charlotte, Charlotte, NC 28223, USA.
Alicia T HamiltonDepartment of Kinesiology, University of North Carolina Charlotte, Charlotte, NC 28223, USA.
Tyrone CeaserDepartment of Kinesiology, University of North Carolina Charlotte, Charlotte, NC 28223, USA.
Kelli J KochanDepartment of Animal Science, Texas A&M University, College Station, TX 77843, USA.
Penny K RiggsDepartment of Animal Science, Texas A&M University, College Station, TX 77843, USA.
J Timothy LightfootDepartment of Health and Kinesiology, Texas A&M University, College Station, TX 77843, USA ; Sydney and JL Huffines Institute for Sports Medicine and Human Performance, Texas A&M University, College Station, TX 77843, USA ; Department of Kinesiology, University of North Carolina Charlotte, Charlotte, NC 28223, USA.
Texas A&M University · USUniversity of North Carolina at Charlotte · US

Funding

GENETIC FACTORS RESPONSIBLE FOR EXERCISE ENDURANCER01AR050085 · NIAMS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI LIGHTFOOT, J TIMOTHY · 2005 to 2009
$1.6M
NIAMS NIH HHS NIAMS AR050085NIAMS NIH HHS R01 AR050085
6 · The paper itself

Abstract

Numerous candidate genes have been suggested in the recent literature with proposed roles in regulation of voluntary physical activity, with little evidence of these genes' functional roles. This study compared the haplotype structure and expression profile in skeletal muscle and brain of inherently high- (C57L/J) and low- (C3H/HeJ) active mice. Expression of nine candidate genes [Actn2, Actn3, Casq1, Drd2, Lepr, Mc4r, Mstn, Papss2, and Glut4 (a.k.a. Slc2a4)] was evaluated via RT-qPCR. SNPs were observed in regions of Actn2, Casq1, Drd2, Lepr, and Papss2; however, no SNPs were located in coding sequences or associated with any known regulatory sequences. In mice exposed to a running wheel, Casq1 (P = 0.0003) and Mstn (P = 0.002) transcript levels in the soleus were higher in the low-active mice. However, when these genes were evaluated in naïve animals, differential expression was not observed, demonstrating a training effect. Among naïve mice, no genes in either tissue exhibited differential expression between strains. Considering that no obvious SNP mechanisms were determined or differential expression was observed, our results indicate that genomic structural variation or gene expression data alone is not adequate to establish any of these genes' candidacy or causality in relation to regulation of physical activity.

Indexed as

Gene Expression RegulationAnimalsBrainGene Expression ProfilingHaplotypesMiceMice, Inbred C3HMice, Inbred C57BLMotor ActivityMuscle, SkeletalPolymorphism, Single Nucleotide

Identifiers

PMID24551844
PMCPMC3914289
OpenAlexW2079247403

What OpenQuestion holds

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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 OpenQuestion graph.