4.8 Article

Sex determination gene transformer regulates the male-female difference in Drosophila fat storage via the adipokinetic hormone pathway

Journal

ELIFE
Volume 10, Issue -, Pages -

Publisher

eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.72350

Keywords

sexual dimorphism; metabolism; lipids; neurons; sex determination; physiology; hormone; D; melanogaster

Categories

Funding

  1. Canadian Institutes of Health Research [PJT-153072]
  2. CIHR Sex and GenderScience chair program [GS4-171365]
  3. Natural Sciences and Engineering Research Council of Canada [RGPIN-2016-04249]
  4. Michael Smith Foundation for Health Research [16876]
  5. Canadian Foundation for Innovation [JELF-34879]

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Sex differences in whole-body fat storage exist in many species, with females storing more fat than males in fruit flies. The sex determination gene transformer (tra) plays a key role in regulating this difference, with its function in neurons, specifically Akh-producing cells (APCs), influencing fat storage in a sex-specific manner. This study identifies the Akh pathway as a mechanism underlying the male-female difference in whole-body triglyceride levels and provides insight into conserved mechanisms of sexual dimorphism in fat storage.
Sex differences in whole-body fat storage exist in many species. For example, Drosophila females store more fat than males. Yet, the mechanisms underlying this sex difference in fat storage remain incompletely understood. Here, we identify a key role for sex determination gene transformer (tra) in regulating the male-female difference in fat storage. Normally, a functional Tra protein is present only in females, where it promotes female sexual development. We show that loss of Tra in females reduced whole-body fat storage, whereas gain of Tra in males augmented fat storage. Tra's role in promoting fat storage was largely due to its function in neurons, specifically the Adipokinetic hormone (Akh)-producing cells (APCs). Our analysis of Akh pathway regulation revealed a male bias in APC activity and Akh pathway function, where this sex-biased regulation influenced the sex difference in fat storage by limiting triglyceride accumulation in males. Importantly, Tra loss in females increased Akh pathway activity, and genetically manipulating the Akh pathway rescued Tra-dependent effects on fat storage. This identifies sex-specific regulation of Akh as one mechanism underlying the male-female difference in whole-body triglyceride levels, and provides important insight into the conserved mechanisms underlying sexual dimorphism in whole-body fat storage.

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