De Novo Transcriptome Analysis Provides Insights into Immune Related Genes and the RIG-I-Like Receptor Signaling Pathway in the Freshwater Planarian (Dugesia japonica)

PLoS One. 2016 Mar 17;11(3):e0151597. doi: 10.1371/journal.pone.0151597. eCollection 2016.

Abstract

Background: The freshwater planarian Dugesia japonica (D. japonica) possesses extraordinary ability to regenerate lost organs or body parts. Interestingly, in the process of regeneration, there is little wound infection, suggesting that D. japonica has a formidable innate immune system. The importance of immune system prompted us to search for immune-related genes and RIG-I-like receptor signaling pathways.

Results: Transcriptome sequencing of D. japonica was performed on an IlluminaHiSeq2000 platform. A total of 27,180 transcripts were obtained by Trinity assembler. CEGMA analysis and mapping of all trimmed reads back to the assembly result showed that our transcriptome assembly covered most of the whole transcriptome. 23,888 out of 27,180 transcripts contained ORF (open reading fragment), and were highly similar to those in Schistosoma mansoni using BLASTX analysis. 8,079 transcripts (29.7%) and 8,668 (31.9%) were annotated by Blast2GO and KEGG respectively. A DYNLRB-like gene was cloned to verify its roles in the immune response. Finally, the expression patterns of 4 genes (RIG-I, TRAF3, TRAF6, P38) in the RIG-I-like receptor signaling pathway were detected, and the results showed they are very likely to be involved in planarian immune response.

Conclusion: RNA-Seq analysis based on the next-generation sequencing technology was an efficient approach to discover critical genes and to understand their corresponding biological functions. Through GO and KEGG analysis, several critical and conserved signaling pathways and genes related to RIG-I-like receptor signaling pathway were identified. Four candidate genes were selected to identify their expression dynamics in the process of pathogen stimulation. These annotated transcripts of D. japonica provide a useful resource for subsequent investigation of other important pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • DEAD-box RNA Helicases / genetics
  • Gene Ontology
  • Helminth Proteins / genetics*
  • Helminth Proteins / immunology
  • Immunity / genetics*
  • In Situ Hybridization
  • Models, Genetic
  • Molecular Sequence Data
  • Planarians / genetics*
  • Planarians / immunology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Amino Acid
  • Signal Transduction / genetics*
  • Signal Transduction / immunology
  • Transcriptome*

Substances

  • Helminth Proteins
  • DEAD-box RNA Helicases

Grants and funding

This work was supported by the National Natural Science Foundation of China (Grant Numbers 31172074, 30700071, 31572263), the Shandong Provincial Natural Science Foundation (Grant Number ZR2010CL002), the Educational Commission of Shandong Province for University Excellent Teacher of International Cooperation Training Project, Young Teacher Support Program in Shandong University of Technology and the Immolife-biotech Co. Ltd. The funder from Immolife-biotech Co. Ltd. only provided support in the form of salaries for Yang An, but did not have any additional role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.