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SRX5813963: GSM3758148: 3A; Homo sapiens; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 42.8M spots, 3.2G bases, 1.1Gb downloads

Submitted by: NCBI (GEO)
Study: Isolated fiber-type transcriptional profiles in human skeletal muscle
show Abstracthide Abstract
Skeletal muscle is a complex heterogeneous tissue comprised of diverse muscle fiber and non-fiber cell types that, in addition to movement, influences other systems such as immunity, metabolism and cognition. We investigated gene expression patterns of resident human skeletal muscle cells using both single-cell RNA-seq and RNA-seq of single muscle fiber dissections from vastus lateralis. We generated transcriptome profiles of the major multinucleated human skeletal muscle fiber-types as well as 11 human skeletal muscle mononuclear cell types, including immune, endothelial, pericyte and satellite cells. We delineated two fibro-adipogenic progenitor cell subtypes that may contribute to heterotopic ossification and muscular dystrophy fibrosis under pathological conditions. An important application of cell type signatures is for computational deconvolution of cell type specific gene expression changes using data from bulk transcriptome experiments. Analysis of transcriptome data from a 12 week resistance exercise training study using these human skeletal muscle cell-type signatures revealed significant changes in specific mononuclear cell-type proportions related to age, sex, acute exercise and training. This characterization of human skeletal muscle cell types will resolve cell-type specific changes in large-scale physical activity muscle transcriptome studies and can further the understanding of the diverse effects of exercise and the pathophysiology of muscle disease. Overall design: Muscle fibers were isolated from biopsies, MHC content of each fiber was determined by SDS-PAGE, and fibers of each fiber-type (I vs. IIa) were pooled for sequencing.
Sample: 3A
SAMN11613341 • SRS4743000 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: TriZol extraction (TRI Reagent, Molecular Research Center, Cincinnati, OH) The SMARTer® Ultra® Low Input RNA kit (Takara, Mountain View, CA) was used to generate cDNA from 9 ng of total RNA. Using the ThruPLEX® DNA-seq kit (Takara), 1-2 ng of double-stranded cDNA was end-repaired and A-tailed to prepare for adaptor ligation. Indexed adaptors were ligated to sample DNA, and the adaptor-ligated DNA library quality was assessed by measuring nanomolar concentration and the fragment size in base pairs. Sequencing was performed on the NextSeq 500 unit (Illumina, San Diego, CA)
Links:
Runs: 1 run, 42.8M spots, 3.2G bases, 1.1Gb
Run# of Spots# of BasesSizePublished
SRR903681642,783,3723.2G1.1Gb2020-01-21

ID:
7815004

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