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Journal of Cell Science
Article . 2004 . Peer-reviewed
Data sources: Crossref
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Alfy, a novel FYVE-domain-containing protein associated with protein granules and autophagic membranes

Authors: Anne, Simonsen; Hanne C G, Birkeland; David J, Gillooly; Noboru, Mizushima; Akiko, Kuma; Tamotsu, Yoshimori; Thomas, Slagsvold; +2 Authors

Alfy, a novel FYVE-domain-containing protein associated with protein granules and autophagic membranes

Abstract

Phosphatidylinositol-3-phosphate [PtdIns(3)P] regulates endocytic and autophagic membrane traffic. In order to understand the downstream effects of PtdIns(3)P in these processes, it is important to identify PtdIns(3)P-binding proteins, many of which contain FYVE zinc-finger domains. Here, we describe a novel giant FYVE-domain-containing protein, named autophagy-linked FYVE protein (Alfy). Alfy is ubiquitously expressed, shares sequence similarity with the Chediak-Higashi-syndrome protein and has putative homologues in flies, nematodes and fission yeast. Alfy binds PtdIns(3)P in vitro and partially colocalizes with PtdIns(3)P in vivo. Unlike most other FYVE-domain proteins, Alfy is not found on endosomes but instead localizes mainly to the nuclear envelope. When HeLa cells are starved or treated with a proteasome inhibitor, Alfy relocalizes to characteristic filamentous cytoplasmic structures located close to autophagic membranes and ubiquitin-containing protein aggregates. By electron microscopy, similar structures can be found within autophagosomes. We propose that Alfy might target cytosolic protein aggregates for autophagic degradation.

Keywords

Proteasome Endopeptidase Complex, DNA, Complementary, Macromolecular Substances, Nuclear Envelope, Molecular Sequence Data, Autophagy-Related Proteins, Membrane Proteins, Intracellular Membranes, Cytoplasmic Granules, Phosphoric Monoester Hydrolases, Protein Structure, Tertiary, Microscopy, Electron, Transmission, Phagosomes, Autophagy, Humans, Chromosomes, Human, Pair 4, Conserved Sequence, Adaptor Proteins, Signal Transducing, HeLa Cells, Protein Binding

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    260
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    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
260
Top 1%
Top 1%
Top 10%
bronze