Abstract

Next generation sequencing technology rapidly developed research applications in the field of plant functional genomics. Several Hypericum spp. with an aim to generate and enhance gene annotations especially for genes coding the enzymes supposedly included in biosynthesis of valuable bioactive compounds were analyzed. The first de novo transcriptome profiling of Hypericum annulatum Moris, H. tomentosum L., H. kalmianum L., and H. androsaemum L. leaves cultivated in vitro was accomplished. All four species with only limited genomic information were selected on the basis of differences in ability to synthesize hypericins and presence of dark nodules accumulating these metabolites with purpose to enrich genomic background of Hypericum spp. H. annulatum was chosen because of high number of the dark nodules and high content of hypericin. H. tomentosum leaves are typical for the presence of only 1–2 dark nodules localized in the apical part. Both H. kalmianum and H. androsaemum lack hypericin and have no dark nodules. Four separated datasets of the pair-end reads were gathered and used for de novo assembly by Trinity program. Assembled transcriptomes were annotated to the public databases Swiss-Prot and non-redundant protein database (NCBI-nr). Gene ontology analysis was performed. Differences of expression levels in the marginal tissues with dark nodules and inner part of leaves lacking these nodules indicate a potential genetic background for hypericin formation as the presumed site of hypericin biosynthesis is in the cells adjacent to these structures. Altogether 165 contigs in H. annulatum and 100 contigs in H. tomentosum were detected as significantly differentially expressed (P < 0.05) and upregulated in the leaf rim tissues containing the dark nodules. The new sequences homologous to octaketide synthase and enzymes catalyzing phenolic oxidative coupling reactions indispensable for hypericin biosynthesis were discovered. The presented transcriptomic sequence data will improve current knowledge about the selected Hypericum spp. with proposed relation to hypericin biosynthesis and will provide a useful resource of genomic information for consequential studies in the field of functional genomics, proteomics and metabolomics.

Highlights

  • Hypericum is the genus with 496 species of plants spread worldwide (Nürk et al, 2013)

  • High-performance liquid chromatography analysis confirmed the presence of hypericins and emodin in hypericin producing spp., H. annulatum, H. tomentosum, and H. perforatum

  • The samples were deposited in NCBI Sequence Read Archive (SRA) with accession numbers SRX1528960 (H. annulatum leaves with dark nodules), SRX1528962 (H. annulatum leaves without dark nodules), SRX1528963 (H. tomentosum leaves with dark nodules), SRX1528964 (H. tomentosum leaves without dark nodules), SRX1528157 (H. androsaemum) and SRX1528958 (H. kalmianum)

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Summary

Introduction

Hypericum is the genus with 496 species of plants spread worldwide (Nürk et al, 2013). The metabolome of leaf tissue samples of ex vitro grown plants from the proximity to the dark nodules in Hypericum perforatum containing hypericin was visualized by the use of matrix-assisted laser desorption/ionization highresolution mass spectrometry (MALDI-HRMS; Kusari et al, 2015). This study suggested the site of hypericin biosynthesis is in dark nodules and adjacent leaf tissues. The localization of hypericin in dark nodules of the leaves of Hypericum spp. cultured in vitro was qualitatively assessed by desorption electrospray ionization mass spectrometry imaging (DESI-MSI). Acetyl-CoA is condensed with seven molecules of malonylCoA to form the octaketide chain. This undergoes specific cyclization to form emodin anthrone, the immediate precursor of hypericin, catalyzed by the octaketide synthase (OKS). Generation sequencing (NGS) method, especially RNASeq (RNA sequencing) used for cDNA identification enables deeper view into biological mechanisms with a potential to reveal unprecedented complexity of the transcriptomes in non-model plants

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