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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-48201

Pertel, T; Hausmann, S; Morger, D; Züger, S; Guerra, J; Lascano, J; Reinhard, C; Santoni, F A; Uchil, P D; Chatel, L; Bisiaux, A; Albert, M L; Strambio-De-Castillia, C; Mothes, W; Pizzato, M; Grütter, M G; Luban, J (2011). TRIM5 is an innate immune sensor for the retrovirus capsid lattice. Nature, 472(7343):361-365.

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Abstract

TRIM5 is a RING domain-E3 ubiquitin ligase that restricts infection by human immunodeficiency virus (HIV)-1 and other retroviruses immediately following virus invasion of the target cell cytoplasm. Antiviral potency correlates with TRIM5 avidity for the retrovirion capsid lattice and several reports indicate that TRIM5 has a role in signal transduction, but the precise mechanism of restriction is unknown. Here we demonstrate that TRIM5 promotes innate immune signalling and that this activity is amplified by retroviral infection and interaction with the capsid lattice. Acting with the heterodimeric, ubiquitin-conjugating enzyme UBC13-UEV1A (also known as UBE2N-UBE2V1), TRIM5 catalyses the synthesis of unattached K63-linked ubiquitin chains that activate the TAK1 (also known as MAP3K7) kinase complex and stimulate AP-1 and NFκB signalling. Interaction with the HIV-1 capsid lattice greatly enhances the UBC13-UEV1A-dependent E3 activity of TRIM5 and challenge with retroviruses induces the transcription of AP-1 and NF-κB-dependent factors with a magnitude that tracks with TRIM5 avidity for the invading capsid. Finally, TAK1 and UBC13-UEV1A contribute to capsid-specific restriction by TRIM5. Thus, the retroviral restriction factor TRIM5 has two additional activities that are linked to restriction: it constitutively promotes innate immune signalling and it acts as a pattern recognition receptor specific for the retrovirus capsid lattice.

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Department of Biochemistry
07 Faculty of Science > Department of Biochemistry
DDC:570 Life sciences; biology
Language:English
Date:2011
Deposited On:01 Jun 2011 13:31
Last Modified:27 Nov 2013 22:29
Publisher:Nature Publishing Group
ISSN:0028-0836
Publisher DOI:10.1038/nature09976
PubMed ID:21512573
Citations:Web of Science®. Times Cited: 170
Google Scholar™
Scopus®. Citation Count: 177

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