Transcriptome sequencing of Zhikong scallop (Chlamys farreri) and comparative transcriptomic analysis with Yesso scallop (Patinopecten yessoensis)

PLoS One. 2013 May 7;8(5):e63927. doi: 10.1371/journal.pone.0063927. Print 2013.

Abstract

Background: Bivalves play an important role in the ecosystems they inhabit and represent an important food source all over the world. So far limited genetic research has focused on this group of animals largely due to the lack of sufficient genetic or genomic resources. Here, we performed de novo transcriptome sequencing to produce the most comprehensive expressed sequence tag resource for Zhikong scallop (Chlamys farreri), and conducted the first transcriptome comparison for scallops.

Results: In a single 454 sequencing run, 1,033,636 reads were produced and then assembled into 26,165 contigs. These contigs were then clustered into 24,437 isotigs and further grouped into 20,056 isogroups. About 47% of the isogroups showed significant matches to known proteins based on sequence similarity. Transcripts putatively involved in growth, reproduction and stress/immune-response were identified through Gene ontology (GO) and KEGG pathway analyses. Transcriptome comparison with Yesso scallop (Patinopecten yessoensis) revealed similar patterns of GO representation. Moreover, 38 putative fast-evolving genes were identified through analyzing the orthologous gene pairs between the two scallop species. More than 46,000 single nucleotide polymorphisms (SNPs) and 350 simple sequence repeats (SSRs) were also detected.

Conclusion: Our study provides the most comprehensive transcriptomic resource currently available for C. farreri. Based on this resource, we performed the first large-scale transcriptome comparison between the two scallop species, C. farreri and P. yessoensis, and identified a number of putative fast-evolving genes, which may play an important role in scallop speciation and/or local adaptation. A large set of single nucleotide polymorphisms and simple sequence repeats were identified, which are ready for downstream marker development. This transcriptomic resource should lay an important foundation for future genetic or genomic studies on C. farreri.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Female
  • Gene Expression Profiling*
  • Gene Library
  • Male
  • Microsatellite Repeats / genetics
  • Molecular Sequence Annotation
  • Pectinidae / genetics*
  • Polymorphism, Single Nucleotide / genetics
  • Sequence Analysis, DNA*
  • Transcriptome / genetics*

Grants and funding

This work was supported by National Basic Research Program of China [973 Program, 2010CB126406], National Natural Science Foundation of China [31172384, 30972239], National High Technology Research and Development Program of China [2012AA092204, 2012AA10405, 2012AA10402, 2012AA10401], Open Project Program of the Key Laboratory of Marine Bio-resources Sustainable Utilization, SCSIO, CAS and Scholarship award for Excellent Doctoral Student granted by China Ministry of Education. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.