FB2025_01 , released February 20, 2025
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Citation
Kiss, V., Jipa, A., Varga, K., Takáts, S., Maruzs, T., Lőrincz, P., Simon-Vecsei, Z., Szikora, S., Földi, I., Bajusz, C., Tóth, D., Vilmos, P., Gáspár, I., Ronchi, P., Mihály, J., Juhász, G. (2020). Drosophila Atg9 regulates the actin cytoskeleton via interactions with profilin and Ena.  Cell Death Differ. 27(5): 1677--1692.
FlyBase ID
FBrf0245495
Publication Type
Research paper
Abstract
Autophagy ensures the turnover of cytoplasm and requires the coordinated action of Atg proteins, some of which also have moonlighting functions in higher eukaryotes. Here we show that the transmembrane protein Atg9 is required for female fertility, and its loss leads to defects in actin cytoskeleton organization in the ovary and enhances filopodia formation in neurons in Drosophila. Atg9 localizes to the plasma membrane anchor points of actin cables and is also important for the integrity of the cortical actin network. Of note, such phenotypes are not seen in other Atg mutants, suggesting that these are independent of autophagy defects. Mechanistically, we identify the known actin regulators profilin and Ena/VASP as novel binding partners of Atg9 based on microscopy, biochemical, and genetic interactions. Accordingly, the localization of both profilin and Ena depends on Atg9. Taken together, our data identify a new and unexpected role for Atg9 in actin cytoskeleton regulation.
PubMed ID
PubMed Central ID
PMC7206052 (PMC) (EuropePMC)
Related Publication(s)
Personal communication to FlyBase

Correction: P{Atg9-3xmCherry} contains UAS too.
Jipa, 2024.3.26, Correction: P{Atg9-3xmCherry} contains UAS too. [FBrf0259118]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Cell Death Differ.
    Title
    Cell Death and Differentiation
    Publication Year
    1994-
    ISBN/ISSN
    1350-9047
    Data From Reference
    Aberrations (1)
    Alleles (11)
    Genes (7)
    Physical Interactions (5)
    Cell Lines (1)
    Natural transposons (1)
    Experimental Tools (4)
    Transgenic Constructs (5)