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The human skeletal muscle transcriptome: sex differences, alternative splicing, and tissue homogeneity assessed with RNA sequencing
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för biokemi och biofysik.ORCID-id: 0000-0003-0839-2451
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för biokemi och biofysik.
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2014 (engelsk)Inngår i: The FASEB Journal, ISSN 0892-6638, E-ISSN 1530-6860, Vol. 28, nr 10, s. 4571-4581Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Human skeletal muscle health is important for quality of life and several chronic diseases, including type II diabetes, heart disease, and cancer. Skeletal muscle is a tissue widely used to study mechanisms behind different diseases and adaptive effects of controlled interventions. For such mechanistic studies, knowledge about the gene expression profiles in different states is essential. Since the baseline transcriptome has not been analyzed systematically, the purpose of this study was to provide a deep reference profile of female and male skeletal muscle. RNA sequencing data were analyzed from a large set of 45 resting human muscle biopsies. We provide extensive information on the skeletal muscle transcriptome, including 5 previously unannotated protein-coding transcripts. Global transcriptional tissue homogeneity was strikingly high, within both a specific muscle and the contralateral leg. We identified >23,000 known isoforms and found >5000 isoforms that differ between the sexes. The female and male transcriptome was enriched for genes associated with oxidative metabolism and protein catabolic processes, respectively. The data demonstrate remarkably high tissue homogeneity and provide a deep and extensive baseline reference for the human skeletal muscle transcriptome, with regard to alternative splicing, novel transcripts, and sex differences in functional ontology.

sted, utgiver, år, opplag, sider
2014. Vol. 28, nr 10, s. 4571-4581
Emneord [en]
gene expression profiling, biopsy, isoform, splice variant, novel transcript
HSV kategori
Identifikatorer
URN: urn:nbn:se:su:diva-108530DOI: 10.1096/fj.14-255000ISI: 000342222700032OAI: oai:DiVA.org:su-108530DiVA, id: diva2:762198
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AuthorCount:6;

Tilgjengelig fra: 2014-11-10 Laget: 2014-10-29 Sist oppdatert: 2022-02-23bibliografisk kontrollert

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Huss, MikaelKjellqvist, Sanela

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