Reference-free population genomics from next-generation transcriptome data and the vertebrate-invertebrate gap

PLoS Genet. 2013 Apr;9(4):e1003457. doi: 10.1371/journal.pgen.1003457. Epub 2013 Apr 11.

Abstract

In animals, the population genomic literature is dominated by two taxa, namely mammals and drosophilids, in which fully sequenced, well-annotated genomes have been available for years. Data from other metazoan phyla are scarce, probably because the vast majority of living species still lack a closely related reference genome. Here we achieve de novo, reference-free population genomic analysis from wild samples in five non-model animal species, based on next-generation sequencing transcriptome data. We introduce a pipe-line for cDNA assembly, read mapping, SNP/genotype calling, and data cleaning, with specific focus on the issue of hidden paralogy detection. In two species for which a reference genome is available, similar results were obtained whether the reference was used or not, demonstrating the robustness of our de novo inferences. The population genomic profile of a hare, a turtle, an oyster, a tunicate, and a termite were found to be intermediate between those of human and Drosophila, indicating that the discordant genomic diversity patterns that have been reported between these two species do not reflect a generalized vertebrate versus invertebrate gap. The genomic average diversity was generally higher in invertebrates than in vertebrates (with the notable exception of termite), in agreement with the notion that population size tends to be larger in the former than in the latter. The non-synonymous to synonymous ratio, however, did not differ significantly between vertebrates and invertebrates, even though it was negatively correlated with genetic diversity within each of the two groups. This study opens promising perspective regarding genome-wide population analyses of non-model organisms and the influence of population size on non-synonymous versus synonymous diversity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Drosophila / genetics*
  • Genome, Human*
  • Genotype
  • Hares / genetics
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Invertebrates / genetics
  • Isoptera / genetics
  • Metagenomics*
  • Ostreidae / genetics
  • Polymorphism, Single Nucleotide
  • Transcriptome / genetics*
  • Turtles / genetics
  • Urochordata / genetics
  • Vertebrates / genetics

Grants and funding

This work was supported by a European Research Council (ERC) grant to NG (ERC PopPhyl 232971). Further support was obtained from the Portuguese Science and Technology Foundation, FCT (project PTDC/BIA-EVF/111931/2009, co-funded by FEDER/COMPETE; post-doc grants SFRH/BPD/43264/2008, PTDC/BIA-EVF/115069/2009 and SFRH/BPD/72343/2010 to JM-F and MC respectively, co-funded by the E. Social Fund). The work of SG and BN was supported by Agropolis Resource Centre for Crop Conservation, Adaptation and Diversity, a flagship project of the Agropolis Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.