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A Drosophila Genome-Wide Screen Identifies Regulators of Steroid Hormone Production and Developmental Timing. | LitMetric

AI Article Synopsis

  • Steroid hormones are crucial for development and are linked to various diseases, prompting a study to identify genes and pathways involved in their production through a genome-wide RNAi screen in fruit flies, discovering 1,906 relevant genes.
  • The research highlights a specific fatty acid elongase that manages cholesterol levels, essential for steroidogenesis, and also uncovers a new mechanism for mobilizing cholesterol that can help mitigate a specific genetic disorder.
  • The study also connects these cholesterol-trafficking processes to the TOR signaling pathway, illustrating how they regulate steroid production and growth, which is important for proper development timing and could impact disease mechanisms.

Article Abstract

Steroid hormones control important developmental processes and are linked to many diseases. To systematically identify genes and pathways required for steroid production, we performed a Drosophila genome-wide in vivo RNAi screen and identified 1,906 genes with potential roles in steroidogenesis and developmental timing. Here, we use our screen as a resource to identify mechanisms regulating intracellular levels of cholesterol, a substrate for steroidogenesis. We identify a conserved fatty acid elongase that underlies a mechanism that adjusts cholesterol trafficking and steroidogenesis with nutrition and developmental programs. In addition, we demonstrate the existence of an autophagosomal cholesterol mobilization mechanism and show that activation of this system rescues Niemann-Pick type C1 deficiency that causes a disorder characterized by cholesterol accumulation. These cholesterol-trafficking mechanisms are regulated by TOR and feedback signaling that couples steroidogenesis with growth and ensures proper maturation timing. These results reveal genes regulating steroidogenesis during development that likely modulate disease mechanisms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918455PMC
http://dx.doi.org/10.1016/j.devcel.2016.05.015DOI Listing

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