FB2024_02 , released April 23, 2024
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Citation
Texada, M.J., Malita, A., Christensen, C.F., Dall, K.B., Faergeman, N.J., Nagy, S., Halberg, K.A., Rewitz, K. (2019). Autophagy-Mediated Cholesterol Trafficking Controls Steroid Production.  Dev. Cell 48(5): 659--671.e4.
FlyBase ID
FBrf0241690
Publication Type
Research paper
Abstract
Steroid hormones are important signaling molecules that regulate growth and drive the development of many cancers. These factors act as long-range signals that systemically regulate the growth of the entire organism, whereas the Hippo/Warts tumor-suppressor pathway acts locally to limit organ growth. We show here that autophagy, a pathway that mediates the degradation of cellular components, also controls steroid production. This process is regulated by Warts (in mammals, LATS1/2) signaling, via its effector microRNA bantam, in response to nutrients. Specifically, autophagy-mediated mobilization and trafficking of the steroid precursor cholesterol from intracellular stores controls the production of the Drosophila steroid ecdysone. Furthermore, we also show that bantam regulates this process via the ecdysone receptor and Tor signaling, identifying pathways through which bantam regulates autophagy and growth. The Warts pathway thus promotes nutrient-dependent systemic growth during development by autophagy-dependent steroid hormone regulation (ASHR). These findings uncover an autophagic trafficking mechanism that regulates steroid production.
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Related Publication(s)
Note

Autophagy regulates steroid production by mediating cholesterol trafficking in endocrine cells.
Texada et al., 2019, Autophagy 15(8): 1478--1480 [FBrf0242754]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Dev. Cell
    Title
    Developmental Cell
    Publication Year
    2001-
    ISBN/ISSN
    1534-5807 1878-1551
    Data From Reference