FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Jipa, A., Vedelek, V., Merényi, Z., Ürmösi, A., Takáts, S., Kovács, A.L., Horváth, G.V., Sinka, R., Juhász, G. (2021). Analysis of Drosophila Atg8 proteins reveals multiple lipidation-independent roles.  Autophagy 17(9): 2565--2575.
FlyBase ID
FBrf0251487
Publication Type
Research paper
Abstract
Yeast Atg8 and its homologs are involved in autophagosome biogenesis in all eukaryotes. These are the most widely used markers for autophagy thanks to the association of their lipidated forms with autophagic membranes. The Atg8 protein family expanded in animals and plants, with most Drosophila species having two Atg8 homologs. In this Brief Report, we use clear-cut genetic analysis in Drosophila melanogaster to show that lipidated Atg8a is required for autophagy, while its non-lipidated form is essential for developmentally programmed larval midgut elimination and viability. In contrast, expression of Atg8b is restricted to the male germline and its loss causes male sterility without affecting autophagy. We find that high expression of non-lipidated Atg8b in the male germline is required for fertility. Consistent with these non-canonical functions of Atg8 proteins, loss of Atg genes required for Atg8 lipidation lead to autophagy defects but do not cause lethality or male sterility.
PubMed ID
PubMed Central ID
PMC8496532 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Autophagy
    Title
    Autophagy
    Publication Year
    2005-
    ISBN/ISSN
    1554-8627 1554-8635
    Data From Reference