Transcriptome analysis of the Portunus trituberculatus: de novo assembly, growth-related gene identification and marker discovery

PLoS One. 2014 Apr 10;9(4):e94055. doi: 10.1371/journal.pone.0094055. eCollection 2014.

Abstract

Background: The swimming crab, Portunus trituberculatus, is an important farmed species in China, has been attracting extensive studies, which require more and more genome background knowledge. To date, the sequencing of its whole genome is unavailable and transcriptomic information is also scarce for this species. In the present study, we performed de novo transcriptome sequencing to produce a comprehensive transcript dataset for major tissues of Portunus trituberculatus by the Illumina paired-end sequencing technology.

Results: Total RNA was isolated from eyestalk, gill, heart, hepatopancreas and muscle. Equal quantities of RNA from each tissue were pooled to construct a cDNA library. Using the Illumina paired-end sequencing technology, we generated a total of 120,137 transcripts with an average length of 1037 bp. Further assembly analysis showed that all contigs contributed to 87,100 unigenes, of these, 16,029 unigenes (18.40% of the total) can be matched in the GenBank non-redundant database. Potential genes and their functions were predicted by GO, KEGG pathway mapping and COG analysis. Based on our sequence analysis and published literature, many putative genes with fundamental roles in growth and muscle development, including actin, myosin, tropomyosin, troponin and other potentially important candidate genes were identified for the first time in this specie. Furthermore, 22,673 SSRs and 66,191 high-confidence SNPs were identified in this EST dataset.

Conclusion: The transcriptome provides an invaluable new data for a functional genomics resource and future biological research in Portunus trituberculatus. The data will also instruct future functional studies to manipulate or select for genes influencing growth that should find practical applications in aquaculture breeding programs. The molecular markers identified in this study will provide a material basis for future genetic linkage and quantitative trait loci analyses, and will be essential for accelerating aquaculture breeding programs with this species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aquaculture
  • Brachyura / genetics*
  • Brachyura / metabolism*
  • China
  • Computational Biology
  • Expressed Sequence Tags
  • Gene Expression Profiling*
  • Gene Library
  • Genetic Markers
  • Genomics
  • Microsatellite Repeats
  • Molecular Sequence Annotation
  • Polymorphism, Single Nucleotide
  • Quantitative Trait Loci
  • Real-Time Polymerase Chain Reaction
  • Sequence Analysis, DNA

Substances

  • Genetic Markers

Grants and funding

Financial support for this study was provided by the National High Technology Research and Development Program of China (Project 2012AA10A409), Agricultural science and Technology Achievements Transformation Fund Project of the Ministry of science and technology (Project 2013GB23260589), the National Natural Science Foundation of China (Grant No. 41306177), the National Science Foundation for Post-doctoral Scientists of China (Project 2013M531657), Special Scientific Research Funds for Central Non-profit Institutes, Yellow Sea Fisheries Research Institute (Project 20603022013039), Projects of independent innovation in Shandong Province (Project 2013CXC80202), Project development of science and technology in Shandong Province (Project 2011GHY11526). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.