4.7 Article

MicroRNA-17-92 Regulates the Transcription Factor E2F3b during Myogenesis In Vitro and In Vivo

Journal

Publisher

MDPI AG
DOI: 10.3390/ijms18040727

Keywords

miR-20a; E2F3b; muscle

Funding

  1. National Basic Research Program of China (973 Program) [2012CB124701]
  2. National Natural Science Foundation of China [81370151, 81570046, 31571199]
  3. Shenzhen Municipal Basic Research Program [JCYJ20150729104027220, JCYJ20160520174217859]
  4. Shenzhen Overseas High-Level Talents Innovation Program [YFZZ20111009]
  5. Shenzhen High-tech Development Project [CXZZ20140828163951592]
  6. Shenzhen University Interdisciplinary Innovation Team Project [000003]
  7. Transgenic Project from the Ministry of Agriculture [2014ZX08009-051B]

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Myogenic differentiation, which occurs during muscle development, is a highly ordered process that can be regulated by E2F transcription factors. Available data show that E2F3b, but not E2F3a, is upregulated and required for myogenic differentiation. However, the regulation of E2F3b expression in myogenic differentiation is not well understood. To investigate whether E2Fb expression is controlled by miRNAs, we used bioinformatics to combine the database of microRNAs downregulated during myogenesis and those predicted to target E2F3. This identified miR-17 and miR-20a as miRNAs potentially involved in E2F3 regulation. We found that miR-17-92 controls the expression of E2F3b in C2C12 cells during myogenic differentiation. Moreover, we confirmed that miR-20a regulates the expression of E2F3b proteins in vivo using a muscle regeneration model.

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