Abstract

Endives (Cichorium endivia L.) are popular vegetables, diversified into curly/frisée- and smooth/broad-leafed (escaroles) cultivar types (cultigroups), and consumed as fresh and bagged salads. They are rich in sesquiterpene lactones (STL) that exert proven function on bitter taste and human health. The assembly of a reference transcriptome of 77,022 unigenes and RNA-sequencing experiments were carried out to characterize the differences between endives and escaroles at the gene structural and expression levels. A set of 3177 SNPs distinguished smooth from curly cultivars, and an SNP-supported phylogenetic tree separated the cultigroups into two distinct clades, consistently with the botanical varieties of origin (crispum and latifolium, respectively). A pool of 699 genes maintained differential expression pattern (core-DEGs) in pairwise comparisons between curly vs smooth cultivars grown in the same environment. Accurate annotation allowed the identification of 26 genes in the sesquiterpenoid biosynthesis pathway, which included several germacreneA synthase, germacreneA oxidase and costunolidesynthase members (GAS/GAO/COS module), required for the synthesis of costunolide, a key precursor of lactucopicrin- and lactucin-like sesquiterpene lactones. The core-DEGs contained a GAS gene (contig83192) that was positively correlated with STL levels and recurrently more expressed in curly than smooth endives, suggesting a cultigroup-specific behavior. The significant positive correlation of GAS/GAO/COS transcription and STL abundance (2.4-fold higher in frisée endives) suggested that sesquiterpenoid pathway control occurs at the transcriptional level. Based on correlation analyses, five transcription factors (MYB, MYB-related and WRKY) were inferred to act on contig83192/GAS and specific STL, suggesting the occurrence of two distinct routes in STL biosynthesis.

Highlights

  • Introduction TheCichorium endivia (L.) species belong to the Asteraceae family and includes the botanical varietiesTestone et al Horticulture Research (2019)6:1 dentate margins

  • Transcriptome features A cDNA library was synthesized from equal quantities of RNA isolated from apical tips, stems, leaves, and roots of C. endivia plants sampled at both transplant and harvest stages (Table 1)

  • The “onestep” procedure consisted of a de novo assembling by Trinity, which led to 255,105 sequences with an N50 and mean contig length of 1586 and 1048 bp, respectively

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Summary

Introduction

Introduction TheCichorium endivia (L.) species belong to the Asteraceae family and includes the botanical varietiesTestone et al Horticulture Research (2019)6:1 dentate margins. The consumption of endives has been increasing in fresh and minimally processed segments worldwide and greatly in Europe, where Italy, Spain, and France are major representatives of Cichorium spp. products The Cichorium spp. genetic consensus map[7] has included markers from a C. intybus × C. endivia cross[4]; molecular marker assisted breeding of endive is expected to increase considering the recent development of genomic tools[8]. Commercialized cultivars mostly consist of pure lines derived from repeated selfings of plants from local populations or of hybrids selected from parental line cross (F1 hybrid production is poorly explored ). Breeding programs are mainly performed by private seed companies to develop varieties suitable for the fresh-salad or minimally processed-salad markets, able to span the whole year cultivation (outdoor or in greenhouse), namely cold resistant in spring and heat tolerant in summer

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