MassIVE MSV000088006

Partial Public PXD028031

Interactomic analysis reveals a new homeostatic role for the HIV restriction factor TRIM5 alpha in mitophagy

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Description

The protein TRIM5 alpha has multiple roles in anti-retroviral defense, but the mechanisms underlying TRIM5 alpha action are unclear. Here, we used an APEX2-based proteomics approach to identify TRIM5 alpha-interacting proteins. Analysis of the TRIM5 alpha interactome found proteins participating in a wide variety of cellular functions including regulating antiviral signaling pathways. We used this data set to uncover a novel role for TRIM5 alpha in mitophagy, an autophagy-based mode of mitochondrial quality control that is compromised in multiple human diseases. Mitochondrial damage triggered the relocalization of TRIM5 alpha to ER-mitochondria contact sites where TRIM5 alpha colocalized with markers of autophagy initiation and autophagosome biogenesis. Furthermore, we found that TRIM5 alpha knockout attenuated both Parkin-dependent and Parkin-independent mitophagy by preventing the recruitment of autophagy regulators FIP200 and ATG13 to unhealthy mitochondria. Finally, TRIM5 alpha knockout cells showed reduced mitochondrial function under basal conditions and were more susceptible to uncontrolled immune activation and cell death in response to mitochondrial damage than were wild type cells. Taken together, our studies have identified a homeostatic role for a protein previously recognized exclusively for its antiviral actions. [doi:10.25345/C51N9S] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: TRIM5a

Contact

Principal Investigators:
(in alphabetical order) 		Michael A Mandell, Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center,, USA
Submitting User: brettsp1
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