A novel terpene synthase produces an anti-aphrodisiac pheromone in the butterflyHeliconius melpomene

التفاصيل البيبلوغرافية
العنوان: A novel terpene synthase produces an anti-aphrodisiac pheromone in the butterflyHeliconius melpomene
المؤلفون: Anna Orteu, Byers Kjrp, Kathy Darragh, Ian A. Warren, Diana Abondano Almeida, Chris D. Jiggins, Ana Pinharanda, Sylvia Fernanda Garza, Richard M. Merrill, Daiane Szczerbowski, John W. Davey, W. O. McMillan, Stefan Schulz, Pasi Rastas
بيانات النشر: Cold Spring Harbor Laboratory, 2019.
سنة النشر: 2019
مصطلحات موضوعية: 0106 biological sciences, Genetics, 0303 health sciences, biology, Phylogenetic tree, Monoterpene, media_common.quotation_subject, fungi, Insect, biology.organism_classification, 010603 evolutionary biology, 01 natural sciences, Hemiptera, Heliconius melpomene, Lepidoptera genitalia, Terpene, 03 medical and health sciences, Pheromone, 030304 developmental biology, media_common
الوصف: Terpenes, a group of structurally diverse compounds, are the biggest class of secondary metabolites. While the biosynthesis of terpenes by enzymes known as terpene synthases (TPSs) has been described in plants and microorganisms, few TPSs have been identified in insects, despite the presence of terpenes in multiple insect species. Indeed, in many insect species, it remains unclear whether terpenes are sequestered from plants or biosynthesisedde novo. No homologs of plant TPSs have been found in insect genomes, though insect TPSs with an independent evolutionary origin have been found in Hemiptera and Coleoptera. In the butterflyHeliconius melpomene, the monoterpene (E)-β-ocimene acts as an anti-aphrodisiac pheromone, where it is transferred during mating from males to females to avoid re-mating by deterring males. To date only one insect monoterpene synthase has been described, inIps pini(Coleoptera), and is a multifunctional TPS and isoprenyl diphosphate synthase (IDS). Here, we combine linkage mapping and expression studies to identify candidate genes involved in the biosynthesis of (E)-β-ocimene. We confirm thatH. melpomenehas two enzymes that exhibit TPS activity, and one of these, HMEL037106g1 is able to synthesise (E)-β-ocimenein vitro. Unlike the enzyme inIps pini, these enzymes only exhibit residual IDS activity, suggesting they are more specialised TPSs, akin to those found in plants. Phylogenetic analysis shows that these enzymes are unrelated to previously described plant and insect TPSs. The distinct evolutionary origin of TPSs in Lepidoptera suggests that they have evolved multiple times in insects.Significance statementTerpenes are a diverse class of natural compounds, used by both plants and animals for a variety of functions, including chemical communication. In insects it is often unclear whether they are synthesisedde novoor sequestered from plants. Some plants and insects have converged to use the same compounds. For instance, (E)-β-ocimene is a common component of floral scent and is also used by the butterflyHeliconius melpomeneas an anti-aphrodisiac pheromone. We describe two novel terpene synthases, one of which synthesises (E)-β-ocimene inH. melpomene, unrelated not only to plant enzymes but also other recently identified insect terpene synthases. This provides the first evidence that the ability to synthesise terpenes has arisen multiple times independently within the insects.
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f4a6c5b2ae23e8193ee85ebbf4f791f
https://doi.org/10.1101/779678
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....2f4a6c5b2ae23e8193ee85ebbf4f791f
قاعدة البيانات: OpenAIRE