Evidence map›Paper›PMID 26109061›Full record

ArticleBMC genomics2015

The human cardiac and skeletal muscle proteomes defined by transcriptomics and antibody-based profiling.

Cecilia Lindskog, Jerker Linné, Linn Fagerberg, Björn M Hallström, Carl Johan Sundberg, Malene Lindholm, Mikael Huss, Caroline Kampf, Howard Choi, David A Liem and 7 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Skeletal Muscle Involvement in Friedreich Ataxia.International journal of molecular sciences · 2024
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Variants inHGG advances · 2023
    Article
  15. Article
  16. Variants inmedRxiv : the preprint server for health sciences · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Article
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

17 authors at 7 institutions in 2 countries.

Cecilia LindskogScience for Life Laboratory, Dept of Immunology Genetics and Pathology, Uppsala University, SE-751 85, Uppsala, Sweden. cecilia.lindskog@igp.uu.se.
Jerker LinnéScience for Life Laboratory, Dept of Immunology Genetics and Pathology, Uppsala University, SE-751 85, Uppsala, Sweden. jerker.linne@igp.uu.se.
Linn FagerbergScience for Life Laboratory, KTH - Royal Institute of Technology, AlbaNova University Center, SE-171 21, Stockholm, Sweden. linn.fagerberg@scilifelab.se.
Björn M HallströmScience for Life Laboratory, KTH - Royal Institute of Technology, AlbaNova University Center, SE-171 21, Stockholm, Sweden. bjorn.hallstrom@scilifelab.se.
Carl Johan SundbergDepartment of Physiology and Pharmacology, Karolinska Institutet, SE-171 77, Stockholm, Sweden. carl.j.sundberg@ki.se.
Malene LindholmDepartment of Physiology and Pharmacology, Karolinska Institutet, SE-171 77, Stockholm, Sweden. Malene.Lindholm@ki.se.
Mikael HussScience for Life Laboratory, Dept of Biochemistry and Biophysics, Stockholm University, Box 1031, SE-17121, Solna, Sweden. mikael.huss@scilifelab.se.
Caroline KampfScience for Life Laboratory, Dept of Immunology Genetics and Pathology, Uppsala University, SE-751 85, Uppsala, Sweden. caroline.kampf@igp.uu.se.
Howard ChoiNHLBI Proteomics Center at UCLA, Departments of Physiology and Medicine, Division of Cardiology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA. cjh9595@ucla.edu.
David A LiemNHLBI Proteomics Center at UCLA, Departments of Physiology and Medicine, Division of Cardiology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA. dliemmd@gmail.com.
Peipei PingNHLBI Proteomics Center at UCLA, Departments of Physiology and Medicine, Division of Cardiology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA. pping@mednet.ucla.edu.
Leif VäremoDepartment of Chemical and Biological Engineering, Chalmers University of Technology, SE-412 58, Gothenburg, Sweden. leif.varemo@chalmers.se.
Adil MardinogluDepartment of Chemical and Biological Engineering, Chalmers University of Technology, SE-412 58, Gothenburg, Sweden. adilm@chalmers.se.
Jens NielsenDepartment of Chemical and Biological Engineering, Chalmers University of Technology, SE-412 58, Gothenburg, Sweden. nielsenj@chalmers.se.
Erik LarssonDepartment of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, SE-751 85, Uppsala, Sweden. erik.larsson@igp.uu.se.
Fredrik PonténScience for Life Laboratory, Dept of Immunology Genetics and Pathology, Uppsala University, SE-751 85, Uppsala, Sweden. fredrik.ponten@igp.uu.se.
Mathias UhlénScience for Life Laboratory, KTH - Royal Institute of Technology, AlbaNova University Center, SE-171 21, Stockholm, Sweden. mathias.uhlen@scilifelab.se.
Science for Life Laboratory · SEUniversity of California, Los Angeles · USChalmers University of Technology · SEKarolinska Institutet · SEAlbaNova · SEKTH Royal Institute of Technology · SEUppsala University · SE

Funding

NHLBI NIH HHS HHSN268201000035CPHS HHS HHSN268201000035C
6 · The paper itself

Abstract

backgroundTo understand cardiac and skeletal muscle function, it is important to define and explore their molecular constituents and also to identify similarities and differences in the gene expression in these two different striated muscle tissues. Here, we have investigated the genes and proteins with elevated expression in cardiac and skeletal muscle in relation to all other major human tissues and organs using a global transcriptomics analysis complemented with antibody-based profiling to localize the corresponding proteins on a single cell level.

resultsOur study identified a comprehensive list of genes expressed in cardiac and skeletal muscle. The genes with elevated expression were further stratified according to their global expression pattern across the human body as well as their precise localization in the muscle tissues. The functions of the proteins encoded by the elevated genes are well in line with the physiological functions of cardiac and skeletal muscle, such as contraction, ion transport, regulation of membrane potential and actomyosin structure organization. A large fraction of the transcripts in both cardiac and skeletal muscle correspond to mitochondrial proteins involved in energy metabolism, which demonstrates the extreme specialization of these muscle tissues to provide energy for contraction.

conclusionsOur results provide a comprehensive list of genes and proteins elevated in striated muscles. A number of proteins not previously characterized in cardiac and skeletal muscle were identified and localized to specific cellular subcompartments. These proteins represent an interesting starting point for further functional analysis of their role in muscle biology and disease.

Indexed as

AntibodiesGene Expression ProfilingHumansMuscle, SkeletalMyocardiumProteomeTranscriptomeAntibodiesProteome

Identifiers

PMID26109061
PMCPMC4479346
OpenAlexW1767363628

What OpenQuestion 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 OpenQuestion graph.