miR-206 is required for changes in cell adhesion that drive muscle cell morphogenesis in Xenopus laevis

Dev Biol. 2018 Jun 15;438(2):94-110. doi: 10.1016/j.ydbio.2018.03.021. Epub 2018 Mar 26.

Abstract

MicroRNAs (miRNAs) are highly conserved small non-coding RNA molecules that post-transcriptionally regulate gene expression in multicellular organisms. Within the set of muscle-specific miRNAs, miR-206 expression is largely restricted to skeletal muscle and is found exclusively within the bony fish lineage. Although many studies have implicated miR-206 in muscle maintenance and disease, its role in skeletal muscle development remains largely unknown. Here, we examine the role of miR-206 during Xenopus laevis somitogenesis. In Xenopus laevis, miR-206 expression coincides with the onset of somitogenesis. We show that both knockdown and over-expression of miR-206 result in abnormal somite formation affecting muscle cell rotation, attachment, and elongation. In particular, our data suggests that miR-206 regulates changes in cell adhesion that affect the ability of newly formed somites to adhere to the notochord as well as to the intersomitic boundaries. Additionally, we show that β-dystroglycan and F-actin expression levels are significantly reduced, suggesting that knockdown of miR-206 levels affects cellular mechanics necessary for cell shape changes and attachments that are required for proper muscle formation.

Keywords: MiR-206; Morphogenesis; Muscle; Somite; Xenopus laevis; β-dystroglycan.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Actins / genetics
  • Animals
  • Cell Adhesion / genetics*
  • Cell Shape / genetics
  • Dystroglycans / genetics
  • Gene Expression Regulation, Developmental / genetics
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Morphogenesis / genetics
  • Muscle Cells / metabolism
  • Muscle Development / genetics
  • Muscles / metabolism
  • Notochord / metabolism
  • Sequence Homology, Nucleic Acid
  • Somites / metabolism*
  • Somites / physiology
  • Xenopus Proteins / genetics
  • Xenopus Proteins / metabolism
  • Xenopus laevis / genetics

Substances

  • Actins
  • MIRN206 microRNA, human
  • MicroRNAs
  • Xenopus Proteins
  • Dystroglycans