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Dissecting myogenin-mediated retinoid X receptor signaling in myogenic differentiation. | LitMetric

Dissecting myogenin-mediated retinoid X receptor signaling in myogenic differentiation.

Commun Biol

Department of Cellular and Molecular Medicine and Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.

Published: June 2020

AI Article Synopsis

  • Understanding how myoblasts (muscle precursor cells) differentiate is crucial for improving muscle regeneration therapies for patients with muscle disorders.
  • Researchers demonstrated that the RXR-selective agonist, bexarotene, boosts myoblast differentiation by enhancing MyoD expression and myogenin protein levels.
  • The study revealed that RXR signaling influences myogenin's activity through epigenetic changes, such as increased histone acetylation, offering insights for potential therapeutic targets to promote muscle regeneration.

Article Abstract

Deciphering the molecular mechanisms underpinning myoblast differentiation is a critical step in developing the best strategy to promote muscle regeneration in patients suffering from muscle-related diseases. We have previously established that a rexinoid x receptor (RXR)-selective agonist, bexarotene, enhances the differentiation and fusion of myoblasts through a direct regulation of MyoD expression, coupled with an augmentation of myogenin protein. Here, we found that RXR signaling associates with the distribution of myogenin at poised enhancers and a distinct E-box motif. We also found an association of myogenin with rexinoid-responsive gene expression and identified an epigenetic signature related to histone acetyltransferase p300. Moreover, RXR signaling augments residue-specific histone acetylation at enhancers co-occupied by p300 and myogenin. Thus, genomic distribution of transcriptional regulators is an important designate for identifying novel targets as well as developing therapeutics that modulate epigenetic landscape in a selective manner to promote muscle regeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303199PMC
http://dx.doi.org/10.1038/s42003-020-1043-9DOI Listing

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