FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Song, J., Mizrak, A., Lee, C.W., Cicconet, M., Lai, Z.W., Tang, W.C., Lu, C.H., Mohr, S.E., Farese, R.V., Walther, T.C. (2022). Identification of two pathways mediating protein targeting from ER to lipid droplets.  Nat. Cell Biol. 24(9): 1364--1377.
FlyBase ID
FBrf0254506
Publication Type
Research paper
Abstract
Pathways localizing proteins to their sites of action are essential for eukaryotic cell organization and function. Although mechanisms of protein targeting to many organelles have been defined, how proteins, such as metabolic enzymes, target from the endoplasmic reticulum (ER) to cellular lipid droplets (LDs) is poorly understood. Here we identify two distinct pathways for ER-to-LD protein targeting: early targeting at LD formation sites during formation, and late targeting to mature LDs after their formation. Using systematic, unbiased approaches in Drosophila cells, we identified specific membrane-fusion machinery, including regulators, a tether and SNARE proteins, that are required for the late targeting pathway. Components of this fusion machinery localize to LD-ER interfaces and organize at ER exit sites. We identified multiple cargoes for early and late ER-to-LD targeting pathways. Our findings provide a model for how proteins target to LDs from the ER either during LD formation or by protein-catalysed formation of membrane bridges.
PubMed ID
PubMed Central ID
PMC9481466 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Cell Biol.
    Title
    Nature Cell Biology
    Publication Year
    1999-
    ISBN/ISSN
    1465-7392 1476-4679
    Data From Reference