Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pgen.1006126
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dc.titleSteroid Hormone Signaling Is Essential for Pheromone Production and Oenocyte Survival
dc.contributor.authorChiang Y.N.
dc.contributor.authorTan K.J.
dc.contributor.authorChung H.
dc.contributor.authorLavrynenko O.
dc.contributor.authorShevchenko A.
dc.contributor.authorYew J.Y.
dc.date.accessioned2020-03-13T05:23:37Z
dc.date.available2020-03-13T05:23:37Z
dc.date.issued2016
dc.identifier.citationChiang Y.N., Tan K.J., Chung H., Lavrynenko O., Shevchenko A., Yew J.Y. (2016). Steroid Hormone Signaling Is Essential for Pheromone Production and Oenocyte Survival. PLoS Genetics 12 (6) : e1006126. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1006126
dc.identifier.issn15537390
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/165385
dc.description.abstractMany of the lipids found on the cuticles of insects function as pheromones and communicate information about age, sex, and reproductive status. In Drosophila, the composition of the information-rich lipid profile is dynamic and changes over the lifetime of an individual. However, the molecular basis of this change is not well understood. To identify genes that control cuticular lipid production in Drosophila, we performed a RNA interference screen and used Direct Analysis in Real Time and gas chromatography mass spectrometry to quantify changes in the chemical profiles. Twelve putative genes were identified whereby transcriptional silencing led to significant differences in cuticular lipid production. Amongst them, we characterized a gene which we name spidey, and which encodes a putative steroid dehydrogenase that has sex- and age-dependent effects on viability, pheromone production, and oenocyte survival. Transcriptional silencing or overexpression of spidey during embryonic development results in pupal lethality and significant changes in levels of the ecdysone metabolite 20-hydroxyecdysonic acid and 20-hydroxyecdysone. In contrast, inhibiting gene expression only during adulthood resulted in a striking loss of oenocyte cells and a concomitant reduction of cuticular hydrocarbons, desiccation resistance, and lifespan. Oenocyte loss and cuticular lipid levels were partially rescued by 20-hydroxyecdysone supplementation. Taken together, these results identify a novel regulator of pheromone synthesis and reveal that ecdysteroid signaling is essential for the maintenance of cuticular lipids and oenocytes throughout adulthood. © 2016 Chiang et al.
dc.publisherPublic Library of Science
dc.sourceUnpaywall 20200320
dc.subject20 hydroxyecdysonic acid
dc.subjectecdysone
dc.subjectecdysterone
dc.subjecthydrocarbon
dc.subjectpheromone
dc.subjectsteroid hormone
dc.subjectsteroid reductase
dc.subjectunclassified drug
dc.subjectecdysterone
dc.subjecthydrocarbon
dc.subjectlipid
dc.subjectoxidoreductase
dc.subjectpheromone
dc.subjectsteroid
dc.subjectadult
dc.subjectadulthood
dc.subjectage
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcell loss
dc.subjectcell survival
dc.subjectcontrolled study
dc.subjectcuticle
dc.subjectdesiccation
dc.subjectDrosophila melanogaster
dc.subjectembryo
dc.subjectembryo development
dc.subjectfemale
dc.subjectgender
dc.subjectgene identification
dc.subjectgene overexpression
dc.subjectgene repression
dc.subjectgene silencing
dc.subjecthormone synthesis
dc.subjectlethality
dc.subjectlifespan
dc.subjectlipogenesis
dc.subjectmale
dc.subjectmass fragmentography
dc.subjectnonhuman
dc.subjectoenocyte
dc.subjectRNA interference
dc.subjectspidey gene
dc.subjectanimal
dc.subjectgenetics
dc.subjectmetabolism
dc.subjectphysiology
dc.subjectreproduction
dc.subjectsexual development
dc.subjectsignal transduction
dc.subjectAnimals
dc.subjectDrosophila melanogaster
dc.subjectEcdysterone
dc.subjectFemale
dc.subjectHydrocarbons
dc.subjectLipids
dc.subjectMale
dc.subjectOxidoreductases
dc.subjectPheromones
dc.subjectReproduction
dc.subjectRNA Interference
dc.subjectSex Characteristics
dc.subjectSignal Transduction
dc.subjectSteroids
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.1371/journal.pgen.1006126
dc.description.sourcetitlePLoS Genetics
dc.description.volume12
dc.description.issue6
dc.description.pagee1006126
dc.published.statePublished
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