Characterization of thermally sensitive miRNAs reveals a central role of the FoxO signaling pathway in regulating the cellular stress response of an extreme stenotherm, Trematomus bernacchii

Mar Genomics. 2019 Dec:48:100698. doi: 10.1016/j.margen.2019.100698. Epub 2019 Jul 12.

Abstract

Despite the lack of an inducible heat shock response (HSR), the Antarctic notothenioid fish, Trematomus bernacchii, has retained a level of physiological plasticity that can at least partially compensate for the effects of acute heat stress. Over the last decade, both physiological and transcriptomic studies have signaled these fish can mitigate the effects of acute heat stress by employing other aspects of the cellular stress response (CSR) that help confer thermotolerance as well as drive homeostatic mechanisms during long-term thermal acclimations. However, the regulatory mechanisms that determine temperature-induced changes in gene expression remain largely unexplored in this species. Therefore, this study utilized next generation sequencing coupled with an in silico approach to explore the regulatory role of microRNAs in governing the transcriptomic level response observed in this Antarctic notothenioid with respect to the CSR. Using RNAseq, we characterized the expression of 125 distinct miRNA orthologues in T. bernacchii gill tissue. Additionally, we identified 12 miRNAs that appear to be thermally responsive based on differential expression (DE) analyses performed between fish acclimated to control (-1.5 °C) and an acute heat stress (+4 °C). We further characterized the functional role of these DE miRNAs using bioinformatics pipelines to identify putative gene targets of the DE miRNAs and subsequent gene set enrichment analyses, which together suggest these miRNAs are involved in regulating diverse aspects of the CSR in T. bernacchii.

Keywords: Antarctica; Cellular stress; MicroRNA; Notothenioid; Stenothermic fish.

MeSH terms

  • Acclimatization
  • Animals
  • Forkhead Box Protein O1 / genetics*
  • Gills
  • Heat-Shock Response*
  • Hot Temperature
  • MicroRNAs / genetics*
  • Nucleic Acid Conformation
  • Perciformes / genetics*
  • Signal Transduction*
  • Transcriptome

Substances

  • Forkhead Box Protein O1
  • MicroRNAs