MicroRNA profiling of antler stem cells in potentiated and dormant states and their potential roles in antler regeneration

Mol Genet Genomics. 2016 Apr;291(2):943-55. doi: 10.1007/s00438-015-1158-8. Epub 2016 Jan 6.

Abstract

MicroRNAs (miRNAs) can effectively regulate gene expression at the post-transcriptional level and play a critical role in tissue growth, development and regeneration. Our previous studies showed that antler regeneration is a stem cell-based process and antler stem cells reside in the periosteum of a pedicle, the permanent bony protuberance, from which antler regeneration takes place. Antlers are the only mammalian organ that can fully regenerate and hence provide a unique opportunity to identify miRNAs that are involved in organ regeneration. In the present study, we used next generation sequencing technology sequenced miRNAs of the stem cells derived from either the potentiated or the dormant pedicle periosteum. A population of both conserved and 20 deer-specific miRNAs was identified. These conserved miRNAs were derived from 453 homologous hairpin precursors across 88 animal species, and were further grouped into 167 miRNA families. Among them, the miR-296 is embryonic stem cell-specific. The potentiation process resulted in the significant regulation (>±2 Fold, q value <0.05) of conserved miRNAs; 8 miRNA transcripts were down- and 6 up-regulated. Several GO biology processes and the Wnt, MAPK and TGF-beta signaling pathways were found to be up-regulated as part of antlerogenic stem cell potentiation process. This research has identified miRNAs that are associated either with the dormant or the potentiated antler stem cells and identified some target miRNAs for further research into their role played in mammalian organ regeneration.

Keywords: Antler; Antler stem cells; Pedicle periosteum; Regeneration; miRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antlers / cytology
  • Antlers / metabolism*
  • Deer / genetics
  • Deer / growth & development
  • High-Throughput Nucleotide Sequencing*
  • MicroRNAs / biosynthesis*
  • MicroRNAs / genetics
  • Regeneration / genetics*
  • Stem Cells / metabolism

Substances

  • MicroRNAs