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A cellular cross-species RNA-seq atlas captures the transcriptional dynamics of myogenesis

GSE324958 Homo sapiens; Mus musculus Expression profiling by high throughput sequencing 24 samples Submitted 2026/03/16 Platform GPL24676Platform GPL24247
Summary
Skeletal muscle formation and regeneration is a tightly regulated process involving extensive transcriptional reprogramming as proliferating myoblasts fuse into mature myotubes. However, a comparative comprehensive analysis of the transcriptional landscape of humans and mouse myogenesis is missing. Here, we present a high-quality RNA-sequencing dataset profiling this transition in both mouse (C2C12) and human (LHCN-M2) myogenic cells. Samples were collected from proliferating myoblasts, the early differentiation phase, and from mature myocytes using identical protocols, ensuring stringent comparability. This unified dataset captures the major transcriptional shifts occurring in myoblasts, marking the onset of differentiation. Quality metrics, including PCA, read distribution, and clustering, confirmed high internal consistency across samples and species. Comparative analyses revealed shared global features of myogenesis but also distinct regulatory trajectories. Human differentiation showed early upregulation followed by suppression of metabolic and stress-related pathways, while structural and ECM-associated programs remained persistently elevated. In contrast, mouse C2C12 cells displayed early inflammatory activation and later enrichment of metabolic and contractile pathways typical of mature myotubes. Ortholog-based integration demonstrated decreasing cross-species correlation over time, indicating progressive reinforcement of species-specific differentiation programs. We additionally compared this bulk RNA-seq with tissue-derived myotubes from single-cell muscle datasets to determine which transcriptional programs are conserved in the in vitro models or which emerge only in vivo. This analysis delineates the conserved and context-specific features of myogenesis, identifying pathways that reflect culture-specific artifacts in both human and mouse muscle cells.
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Direct links to NCBI, no account and no request form: the whole study as GSE324958_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 24 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1438151 and SRA study SRP684092. Searching any of these in the dataset finder brings you back here.

Study design
6 conditions, mostly with about 4 replicates each
C2C12, day0 ×4 C2C12, day1 ×4 C2C12, day6 ×4 LHCNM2, day0 ×4 LHCNM2, day1 ×4 LHCNM2, day12 ×4

Supports a between-group comparison across 24 samples.

6 replicated groups read from 24 sample titles; they account for 24 of them. Check it against the sample list below before relying on it.

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