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pmid:26697350

Genomic-wide transcriptional profiling in primary myoblasts reveals Runx1-regulated genes in muscle regeneration.

Kfir Baruch Umansky · Ester Feldmesser · Yoram Groner

Genomics data · 2015 doi:10.1016/j.gdata.2015.08.030

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Genomic-wide transcriptional profiling in primary myoblasts reveals Runx1-regulated genes in muscle regeneration.
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10.1016/j.gdata.2015.08.030
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Kfir Baruch Umansky
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Ester Feldmesser
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Yoram Groner
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2015
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In response to muscle damage the muscle adult stem cells are activated and differentiate into myoblasts that regenerate the damaged tissue. We have recently showed that following myopathic damage the level of the Runx1 transcription factor (TF) is elevated and that during muscle regeneration this TF regulates the balance between myoblast proliferation and differentiation (Umansky et al.). We employed Runx1-dependent gene expression, Chromatin Immunoprecipitation sequencing (ChIP-seq), Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq) and histone H3K4me1/H3K27ac modification analyses to identify a subset of Runx1-regulated genes that are co-occupied by the TFs MyoD and c-Jun and are involved in muscle regeneration (Umansky et al.). The data is available at the GEO database under the superseries accession number GSE56131.
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Using in vivo loss- and gain-of-function models and genome-wide transcriptional analyses we identify a subset of Runx1-regulateed genes that participate in muscle regeneration.
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GSEA analysis of genes bound by all three TFs in comparison to Runx1-responsive genes in proliferating PMs (A) or gene expression data of WT myoblasts vs. differentiated myotubes (B).
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Transcription factor Runx1 cooperates with MyoD and c-Jun to regulate the balance of myoblast proliferation/differentiation
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Complete file
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We have recently showed that following myopathic damage the level of the Runx1 transcription factor (TF) is elevated and that during muscle regeneration this TF regulates the balance between myoblast proliferation and differentiation (Umansky et al.). We employed Runx1-dependent gene expression, Chromatin Immunoprecipitation sequencing (ChIP-seq), Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq) and histone H3K4me1/H3K27ac modification analyses to identify a subset of Runx1-regulated genes that are co-occupied by the TFs MyoD and c-Jun and are involved in muscle regeneration (Umansky et al.). 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