Evidence map›Paper›PMID 25572546›Full record

ArticlePhysiological genomics2015

Gene expression changes controlling distinct adaptations in the heart and skeletal muscle of a hibernating mammal.

Katie L Vermillion, Kyle J Anderson, Marshall Hampton, Matthew T Andrews

Open access · greenAbstract read
In one paragraph

Article in Physiological genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 75 citations in OpenAlex.

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  9. Extensive longevity and DNA virus-driven adaptation in nearcticbioRxiv : the preprint server for biology · 2025
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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

4 authors at 1 institution in 1 country.

Katie L VermillionDepartment of Biology, University of Minnesota Duluth, Duluth, Minnesota; and.
Kyle J AndersonDepartment of Biology, University of Minnesota Duluth, Duluth, Minnesota; and.
Marshall HamptonDepartment of Mathematics and Statistics, University of Minnesota Duluth, Duluth, Minnesota.
Matthew T AndrewsDepartment of Biology, University of Minnesota Duluth, Duluth, Minnesota; and mandrews@d.umn.edu.
University of Minnesota, Duluth · US

Funding

Genetic Control of Heart Function in a Hibernating MammalRC2HL101625 · NHLBI · UNIVERSITY OF MINNESOTA DULUTH · PI ANDREWS, MATTHEW T. · 2009 to 2010
$1.2M
NHLBI NIH HHS 1RC2HL-101625-01NHLBI NIH HHS RC2 HL101625
6 · The paper itself

Abstract

Throughout the hibernation season, the thirteen-lined ground squirrel (Ictidomys tridecemlineatus) experiences extreme fluctuations in heart rate, metabolism, oxygen consumption, and body temperature, along with prolonged fasting and immobility. These conditions necessitate different functional requirements for the heart, which maintains contractile function throughout hibernation, and the skeletal muscle, which remains largely inactive. The adaptations used to maintain these contractile organs under such variable conditions serves as a natural model to study a variety of medically relevant conditions including heart failure and disuse atrophy. To better understand how two different muscle tissues maintain function throughout the extreme fluctuations of hibernation we performed Illumina HiSeq 2000 sequencing of cDNAs to compare the transcriptome of heart and skeletal muscle across the circannual cycle. This analysis resulted in the identification of 1,076 and 1,466 differentially expressed genes in heart and skeletal muscle, respectively. In both heart and skeletal muscle we identified a distinct cold-tolerant mechanism utilizing peroxisomal metabolism to make use of elevated levels of unsaturated depot fats. The skeletal muscle transcriptome also shows an early increase in oxidative capacity necessary for the altered fuel utilization and increased oxygen demand of shivering. Expression of the fetal gene expression profile is used to maintain cardiac tissue, either through increasing myocyte size or proliferation of resident cardiomyocytes, while skeletal muscle function and mass are protected through transcriptional regulation of pathways involved in protein turnover. This study provides insight into how two functionally distinct muscles maintain function under the extreme conditions of mammalian hibernation.

Indexed as

Gene Expression ProfilingGene Expression RegulationAdaptation, PhysiologicalAnimalsCluster AnalysisFatty AcidsFetusGlycolysisHeartHibernationMolecular Sequence AnnotationMuscle, SkeletalOligonucleotide Array Sequence AnalysisOrgan SpecificityOxidation-ReductionPeroxisomesFatty AcidsRNA, Messengerhearthibernationskeletal muscletranscriptomics

Identifiers

PMID25572546
PMCPMC4346737
OpenAlexW2167763573

What OpenQuestion holds

Textmetadata
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.