Convergence and divergence of bitterness biosynthesis and regulation in Cucurbitaceae

Differentiation of secondary metabolite profiles in closely related plant species provides clues for unravelling biosynthetic pathways and regulatory circuits, an area that is still underinvestigated. Cucurbitacins, a group of bitter and highly oxygenated tetracyclic triterpenes, are mainly produced by the plant family Cucurbitaceae. These compounds have similar structures, but differ in their antitumour activities and ecophysiological roles. By comparative analyses of the genomes of cucumber, melon and watermelon, we uncovered conserved syntenic loci encoding metabolic genes for distinct cucurbitacins. Characterization of the cytochrome P450s (CYPs) identified from these loci enabled us to unveil a novel multi-oxidation CYP for the tailoring of the cucurbitacin core skeleton as well as two other CYPs responsible for the key structural variations among cucurbitacins C, B and E. We also discovered a syntenic gene cluster of transcription factors that regulates the tissue-specific biosynthesis of cucurbitacins and may confer the loss of bitterness phenotypes associated with convergent domestication of wild cucurbits. This study illustrates the potential to exploit comparative genomics to identify enzymes and transcription factors that control the biosynthesis of structurally related yet unique natural products.

[1]  A. M. Rhodes,et al.  Cucurbitacins as kairomones for diabroticite beetles. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[2]  Anne Osbourn,et al.  Plant metabolic clusters - from genetics to genomics. , 2016, The New phytologist.

[3]  Jian Chao Chen,et al.  Cucurbitacins and cucurbitane glycosides: structures and biological activities. , 2005, Natural product reports.

[4]  D. Sandham A revolution in the making? [WiMax standards] , 2006 .

[5]  Hadi Quesneville,et al.  Formation of plant metabolic gene clusters within dynamic chromosomal regions , 2011, Proceedings of the National Academy of Sciences.

[6]  A. Aharoni,et al.  Biosynthesis of Antinutritional Alkaloids in Solanaceous Crops Is Mediated by Clustered Genes , 2013, Science.

[7]  O. Katare,et al.  Preparation and Pharmacological Evaluation of Silibinin Liposomes , 2003, Arzneimittelforschung.

[8]  V. De Luca,et al.  Mining the Biodiversity of Plants: A Revolution in the Making , 2012, Science.

[9]  K. Nakanishi,et al.  Ginkgolide derivatives for photolabeling studies: preparation and pharmacological evaluation. , 2002, Journal of medicinal chemistry.

[10]  A. Osbourn,et al.  Metabolic Diversification—Independent Assembly of Operon-Like Gene Clusters in Different Plants , 2008, Science.

[11]  Anthony M. Bolger,et al.  Evolution of a Complex Locus for Terpene Biosynthesis in Solanum[W][OPEN] , 2013, Plant Cell.

[12]  M Frey,et al.  Analysis of a chemical plant defense mechanism in grasses. , 1997, Science.

[13]  G. Challis,et al.  Strategies for the Discovery of New Natural Products by Genome Mining , 2009, Chembiochem : a European journal of chemical biology.

[14]  J. Keasling,et al.  High-level semi-synthetic production of the potent antimalarial artemisinin , 2013, Nature.

[15]  Asan,et al.  The genome of the cucumber, Cucumis sativus L. , 2009, Nature Genetics.

[16]  J. Bohlmann,et al.  Genes, enzymes and chemicals of terpenoid diversity in the constitutive and induced defence of conifers against insects and pathogens. , 2006, The New phytologist.

[17]  Y. Ebizuka,et al.  Cucurbitadienol synthase, the first committed enzyme for cucurbitacin biosynthesis, is a distinct enzyme from cycloartenol synthase for phytosterol biosynthesis , 2004 .

[18]  G. Lester Melon (Cucumis melo L.) fruit nutritional quality and health functionality , 1996 .

[19]  G. Ruxton,et al.  Coevolution can explain defensive secondary metabolite diversity in plants. , 2015, The New phytologist.

[20]  Mingyao Liu,et al.  Cucurbitacin E, a tetracyclic triterpenes compound from Chinese medicine, inhibits tumor angiogenesis through VEGFR2-mediated Jak2-STAT3 signaling pathway. , 2010, Carcinogenesis.

[21]  Vasiliki Falara,et al.  The Tomato Terpene Synthase Gene Family1[W][OA] , 2011, Plant Physiology.

[22]  Günter Theißen,et al.  Molecular mechanisms involved in convergent crop domestication. , 2013, Trends in plant science.

[23]  Seung Y. Rhee,et al.  Genomic Signatures of Specialized Metabolism in Plants , 2014, Science.

[24]  C. Bokemeyer,et al.  Cucurbitacin B, a novel in vivo potentiator of gemcitabine with low toxicity in the treatment of pancreatic cancer , 2010, British journal of pharmacology.

[25]  Timothy S. Ham,et al.  Production of the antimalarial drug precursor artemisinic acid in engineered yeast , 2006, Nature.

[26]  R. Gregg,et al.  In vitro myotoxicity of the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, pravastatin, lovastatin, and simvastatin, using neonatal rat skeletal myocytes. , 1995, Toxicology and applied pharmacology.

[27]  S. Mafu,et al.  To gibberellins and beyond! Surveying the evolution of (di)terpenoid metabolism. , 2014, Annual review of plant biology.

[28]  Jin-jian Lu,et al.  Biological activities and potential molecular targets of cucurbitacins: a focus on cancer , 2012, Anti-cancer drugs.

[29]  Xiaoquan Qi,et al.  Biosynthesis, regulation, and domestication of bitterness in cucumber , 2014, Science.

[30]  R. Guigó,et al.  The genome of melon (Cucumis melo L.) , 2012, Proceedings of the National Academy of Sciences.

[31]  J. Jeyapalan WHO focus on cancer , 2001 .

[32]  W. J. Lucas,et al.  The draft genome of watermelon (Citrullus lanatus) and resequencing of 20 diverse accessions , 2012, Nature Genetics.

[33]  T. Winzer,et al.  A Papaver somniferum 10-Gene Cluster for Synthesis of the Anticancer Alkaloid Noscapine , 2012, Science.

[34]  R. Okamoto,et al.  Cucurbitacin B induces apoptosis by inhibition of the JAK/STAT pathway and potentiates antiproliferative effects of gemcitabine on pancreatic cancer cells. , 2009, Cancer research.

[35]  A. Demilo,et al.  Rapid high-performance liquid chromatography method to quantitate elaterinide in juice and reconstituted residues from a bitter mutant of hawkesbury watermelon. , 1999, Journal of agricultural and food chemistry.

[36]  C. M. Jones,et al.  Cucumber Beetle Resistance and Mite Susceptibility Controlled by the Bitter Gene in Cucumis sativus L , 1971, Science.

[37]  P. G. Rao,et al.  Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents. , 2010, Chemical Society reviews.