4.5 Article

Transcriptomic and epigenomics atlas of myotubes reveals insight into the circadian control of metabolism and development

Journal

EPIGENOMICS
Volume 12, Issue 8, Pages 701-713

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/epi-2019-0391

Keywords

C2C12; circadian; epigenetics; methylation; muscle; myotube; transcriptomics

Funding

  1. Novo Nordisk Foundation [NNF18CC003490]
  2. Novo Nordisk Foundation Challenge Grant [NNF14OC0011493]
  3. Swedish Research Council [2015-00165]
  4. Swedish Research Council [2015-00165] Funding Source: Swedish Research Council

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Aim: Innate circadian rhythms are critical for optimal tissue-specific functions, including skeletal muscle, a major insulin-sensitive tissue responsible for glucose homeostasis. We determined whether transcriptional oscillations are associated with CpG methylation changes in skeletal muscle. Materials & methods: We performed rhythmicity analysis on the transcriptome and CpG methylome of circadian synchronized myotubes. Results: We identified several transcripts and CpG-sites displaying oscillatory behavior, which were enriched with Gene Ontology terms related to metabolism and development. Oscillating CpG methylation was associated with rhythmic expression of 31 transcripts. Conclusion: Although circadian oscillations may be regulated by rhythmic DNA methylation, strong rhythmic associations between transcriptome and CpG methylation were not identified. This resource constitutes a transcriptomic/epigenomic atlas of skeletal muscle and regulation of circadian rhythms.

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