Immunity
Volume 36, Issue 6, 29 June 2012, Pages 933-946
Journal home page for Immunity

Article
The Mitochondrial Proteins NLRX1 and TUFM Form a Complex that Regulates Type I Interferon and Autophagy

https://doi.org/10.1016/j.immuni.2012.03.025Get rights and content
Under an Elsevier user license
open archive

Summary

The mitochondrial protein MAVS (also known as IPS-1, VISA, and CARDIF) interacts with RIG-I-like receptors (RLRs) to induce type I interferon (IFN-I). NLRX1 is a mitochondrial nucleotide-binding, leucine-rich repeats (NLR)-containing protein that attenuates MAVS-RLR signaling. Using Nlrx1−/− cells, we confirmed that NLRX1 attenuated IFN-I production, but additionally promoted autophagy during viral infection. This dual function of NLRX1 paralleled the previously described functions of the autophagy-related proteins Atg5-Atg12, but NLRX1 did not associate with Atg5-Atg12. High-throughput quantitative mass spectrometry and endogenous protein-protein interaction revealed an NLRX1-interacting partner, mitochondrial Tu translation elongation factor (TUFM). TUFM interacted with Atg5-Atg12 and Atg16L1 and has similar functions as NLRX1 by inhibiting RLR-induced IFN-I but promoting autophagy. In the absence of NLRX1, increased IFN-I and decreased autophagy provide an advantage for host defense against vesicular stomatitis virus. This study establishes a link between an NLR protein and the viral-induced autophagic machinery via an intermediary partner, TUFM.

Highlights

► NLRX1 suppresses VSV-mediated type 1 IFN production but enhances autophagy ► TUFM works with NLRX1 to inhibit RLR-induced type 1 IFN signaling ► TUFM enhances autophagy and interacts with Atg5-Atg12 and Atg16L1 ► NLRX1-mediated autophagy and IFN-I inhibition enhance VSV replication

Cited by (0)

8

Present address: Department of Diagnostic Sciences, School of Dental Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA

9

These authors contributed equally to this work