Novel insights into molecular mechanisms of Pseudourostyla cristata encystment using comparative transcriptomics

Sci Rep. 2019 Dec 13;9(1):19109. doi: 10.1038/s41598-019-55608-7.

Abstract

The encystment of many ciliates is an advanced survival strategy against adversity and the most important reason for ciliates existence worldwide. However, the molecular mechanism for the encystment of free-living ciliates is poorly understood. Here, we performed comparative transcriptomic analysis of dormant cysts and trophonts from Pseudourostyla cristata using transcriptomics, qRT-PCR and bioinformatic techniques. We identified 2565 differentially expressed unigenes between the dormant cysts and the trophonts. The total number of differentially expressed genes in GO database was 1752. The differential unigenes noted to the GO terms were 1993. These differential categories were mainly related to polyamine transport, pectin decomposition, cytoplasmic translation, ribosome, respiratory chain, ribosome structure, ion channel activity, and RNA ligation. A total of 224 different pathways were mapped. Among them, 184 pathways were upregulated, while 162 were downregulated. Further investigation showed that the calcium and AMPK signaling pathway had important induction effects on the encystment. In addition, FOXO and ubiquitin-mediated proteolysis signaling pathway jointly regulated the encystment. Based on these findings, we propose a hypothetical signaling network that regulates Pseudourostyla cristata encystment. Overall, these results provide deeper insights into the molecular mechanisms of ciliates encystment and adaptation to adverse environments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Calcium / metabolism
  • Cilia / metabolism
  • Ciliophora / genetics
  • Ciliophora / metabolism*
  • Computational Biology
  • Cytoplasm / metabolism
  • Forkhead Box Protein O1 / metabolism
  • Gene Expression Profiling
  • Glutathione Peroxidase / metabolism
  • Microscopy, Electron, Scanning
  • RNA / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ribosomes / metabolism
  • Sequence Analysis, RNA
  • Signal Transduction*
  • Superoxide Dismutase / metabolism
  • Transcriptome*
  • Ubiquitin / metabolism

Substances

  • Forkhead Box Protein O1
  • Ubiquitin
  • RNA
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • AMP-Activated Protein Kinases
  • Calcium