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The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.

TRIM Proteins Regulate Autophagy and Can Target Autophagic Substrates by Direct Recognition

Open access
Mandell, Michael A., Jain, Ashish, Arko-Mensah, John, Chauhan, Santosh, Kimura, Tomonori, Dinkins, Christina, Silvestri, Guido, Münch, Jan, Kirchhoff, Frank, Simonsen, Anne, Wei, Yongjie, Levine, Beth, Johansen, Terje, Deretic, Vojo·2014·Developmental Cell

Abstract

SUMMARY Autophagy, a homeostatic process whereby eukaryotic cells target cytoplasmic cargo for degradation, plays a broad role in health and disease states. Here we screened the TRIM family for roles in autophagy and found that half of TRIMs modulated autophagy. In mechanistic studies we show that TRIMs associate with autophagy factors and act as platforms assembling ULK1 and Beclin 1 in their activated states. Furthermore, TRIM5α acts as a selective autophagy receptor. Based on direct sequence-specific recognition, TRIM5α delivered its cognate cytosolic target, a viral capsid protein, for autophagic degradation. Thus, our study establishes that TRIMs can function both as regulators of autophagy and as autophagic cargo receptors, and reveals a new basis for selective autophagy in mammalian cells.

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Crossref · 10.1016/j.devcel.2014.06.013

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Metadata

Authors
Mandell, M. A., Jain, A., Arko-Mensah, J., Chauhan, S., Kimura, T., Dinkins, C., Silvestri, G., Münch, J., Kirchhoff, F., Simonsen, A., Wei, Y., Levine, B., Johansen, T., & Deretic, V.
Venue
Developmental Cell
Publisher
Elsevier BV
Published
2014-08
Volume
30
Issue
4
Pages
394-409
ISSN
1534-5807 (ISSN-L)
OpenAlex
W2127187639
Cited by
329
References
17
FWCI
19.55
Type
journal article
Language
en
Open access
bronze

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