Abstract

BackgroundUnicellular dinoflagellates are an important group of primary producers within the marine plankton community. Many of these species are capable of forming harmful algae blooms (HABs) and of producing potent phycotoxins, thereby causing deleterious impacts on their environment and posing a threat to human health. The recently discovered toxigenic dinoflagellate Azadinium spinosum is known to produce azaspiracid toxins. These toxins are most likely produced by polyketide synthases (PKS). Recently, PKS I-like transcripts have been identified in a number of dinoflagellate species. Despite the global distribution of A. spinosum, little is known about molecular features. In this study, we investigate the genomic and transcriptomic features of A. spinosum with a focus on polyketide synthesis and PKS evolution.ResultsWe identify orphan and homologous genes by comparing the transcriptome data of A. spinosum with a diverse set of 18 other dinoflagellates, five further species out of the Rhizaria Alveolate Stramelopile (RAS)-group, and one representative from the Plantae. The number of orphan genes in the analysed dinoflagellate species averaged 27%. In contrast, within the A. spinosum transcriptome, we discovered 12,661 orphan transcripts (18%). The dinoflagellates toxins known as azaspiracids (AZAs) are structurally polyethers; we therefore analyse the transcriptome of A. spinosum with respect to polyketide synthases (PKSs), the primary biosynthetic enzymes in polyketide synthesis. We find all the genes thought to be potentially essential for polyketide toxin synthesis to be expressed in A. spinosum, whose PKS transcripts fall into the dinoflagellate sub-clade in PKS evolution.ConclusionsOverall, we demonstrate that the number of orphan genes in the A. spinosum genome is relatively small compared to other dinoflagellate species. In addition, all PKS domains needed to produce the azaspiracid carbon backbone are present in A. spinosum. Our study underscores the extraordinary evolution of such gene clusters and, in particular, supports the proposed structural and functional paradigm for PKS Type I genes in dinoflagellates.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-014-1205-6) contains supplementary material, which is available to authorized users.

Highlights

  • Unicellular dinoflagellates are an important group of primary producers within the marine plankton community

  • Features of the Azadinium spinosum genome The 454-shotgun sequencing on a GS Junior System yielded 103,860 high quality genomic reads (37 Mb) (GenBank accession number: SRR1576789)

  • The dataset provided substantial insights into the genomic structure and organization of A. spinosum, the total coverage was rather low for such a big genome

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Summary

Introduction

Unicellular dinoflagellates are an important group of primary producers within the marine plankton community. Many of these species are capable of forming harmful algae blooms (HABs) and of producing potent phycotoxins, thereby causing deleterious impacts on their environment and posing a threat to human health. The recently discovered toxigenic dinoflagellate Azadinium spinosum is known to produce azaspiracid toxins. These toxins are most likely produced by polyketide synthases (PKS). Dinoflagellate genomes are among the largest known among eukaryotes, ranging in size from 1.5 to 245 Gbp [11]. In addition to the structural peculiarities, the large genome size, high gene copy numbers, and a high content of repetitive genomic elements have made genome sequencing and assembly for dinoflagellate species a difficult task. Additional Transcriptomic studies (e.g. [13]) are beginning to focus research towards in-depth analysis of gene content in dinoflagellates

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