The Ecdysteroidome of Drosophila: influence of diet and development

Author:

Lavrynenko Oksana12,Rodenfels Jonathan13,Carvalho Maria14,Dye Natalie A.1,Lafont Rene5,Eaton Suzanne1,Shevchenko Andrej1

Affiliation:

1. Max Planck Institute for Cell Biology and Genetics, Pfotenhauerstraße 108, 01307, Dresden, Germany

2. present address: Nestlé Institute of Health Sciences S.A, EPFL Innovation Park, Bâtiment H, 1015, Lausanne, Switzerland

3. present address: Molecular Biophysics & Biochemistry Department, Yale University, 333 Ceder Street, New Haven, CT, 06520, USA

4. present address: Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6, 2780-156, Oeiras, Portugal

5. Sorbonne Universités, UPMC Univ Paris 06, IBPS-BIOSIPE, 7 Quai Saint Bernard, Case Courrier 29, 75252 Paris Cedex 05, France

Abstract

Ecdysteroids are the hormones regulating development, physiology and fertility in arthropods, which synthesize them exclusively from dietary sterols. But how dietary sterol diversity influences the ecdysteroid profile, how animals ensure the production of desired hormones and whether there are functional differences between different ecdysteroids produced in vivo, remains unknown. This is because currently there is no analytical technology for unbiased, comprehensive and quantitative assessment of the full complement of endogenous ecdysteroids. We developed a new LC-MS/MS method to screen the entire chemical space of ecdysteroid-related structures and to quantify known and newly discovered hormones and their catabolites. We quantified the ecdysteroidome in Drosophila melanogaster and investigated how the ecdysteroid profile varies with diet and development. We show that Drosophila can produce 4 different classes of ecdysteroids, which are obligatorily derived from 4 types of dietary sterol precursors. Drosophila produces makisterone A from plant sterols and epi-makisterone A from ergosterol, the major yeast sterol. However they prefer to selectively utilize scarce ergosterol precursors to make a novel hormone 24,28-dehydromakisterone A and trace cholesterol to synthesize 20-hydroxyecdysone. Interestingly, epi-makisterone A supports only larval development, while all other ecdysteroids allow full adult development. We suggest that evolutionary pressure against producing epi-C24 ecdysteroids may explain selective utilization of ergosterol precursors and the puzzling preference for cholesterol.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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