Mid Sweden University

miun.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
High-throughput muscle fiber typing from RNA sequencing data
Lund Univ, Dept Clin Sci, Malmö, Sweden.;Lund Univ, Dept Biol, Sci Life Lab, Natl Bioinformat Infrastruct Sweden, Lund, Sweden..
Max Planck Inst Evolutionary Anthropol, Leipzig, Germany..
Univ S Florida, Hlth Informat Inst, Morsani Coll Med, Gainesville, FL USA..
Lund Univ, Dept Clin Sci, Malmö, Sweden..
Show others and affiliations
2022 (English)In: Skeletal Muscle, ISSN 2044-5040, Vol. 12, no 1, article id 16Article in journal (Refereed) Published
Abstract [en]

Background: Skeletal muscle fiber type distribution has implications for human health, muscle function, and performance. This knowledge has been gathered using labor-intensive and costly methodology that limited these studies. Here, we present a method based on muscle tissue RNA sequencing data (totRNAseq) to estimate the distribution of skeletal muscle fiber types from frozen human samples, allowing for a larger number of individuals to be tested. Methods: By using single-nuclei RNA sequencing (snRNAseq) data as a reference, cluster expression signatures were produced by averaging gene expression of cluster gene markers and then applying these to totRNAseq data and inferring muscle fiber nuclei type via linear matrix decomposition. This estimate was then compared with fiber type distribution measured by ATPase staining or myosin heavy chain protein isoform distribution of 62 muscle samples in two independent cohorts (n = 39 and 22). Results: The correlation between the sequencing-based method and the other two were r(ATpas) = 0.44 [0.13-0.67], [95% CI], and r(myosin) = 0.83 [0.61-0.93], with p = 5.70 x 10(-3) and 2.00 x 10(-6), respectively. The deconvolution inference of fiber type composition was accurate even for very low totRNAseq sequencing depths, i.e., down to an average of similar to 10,000 paired-end reads. Conclusions: This new method (https://github.com/OlaHanssonLab/PredictFiberType) consequently allows for measurement of fiber type distribution of a larger number of samples using totRNAseq in a cost and labor-efficient way. It is now feasible to study the association between fiber type distribution and e.g. health outcomes in large well-powered studies.

Place, publisher, year, edition, pages
2022. Vol. 12, no 1, article id 16
National Category
Cell Biology
Identifiers
URN: urn:nbn:se:miun:diva-45742DOI: 10.1186/s13395-022-00299-4ISI: 000820254000001PubMedID: 35780170Scopus ID: 2-s2.0-85133403486OAI: oai:DiVA.org:miun-45742DiVA, id: diva2:1685321
Available from: 2022-08-02 Created: 2022-08-02 Last updated: 2022-08-02Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Ström, Kristoffer

Search in DiVA

By author/editor
Ström, Kristoffer
By organisation
Department of Health Sciences (HOV)
In the same journal
Skeletal Muscle
Cell Biology

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 33 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf