TRIM2 E3 ligase substrate discovery reveals zinc-mediated regulation of TMEM106B in the endolysosomal pathway

Title data

Perez-Borrajero, Cecilia ; Stein, Frank ; Schweimer, Kristian ; Rettel, Mandy ; Schwarz, Jennifer J. ; Haberkant, Per ; Lapouge, Karine ; Gayk, Jesse ; Hoffmann, Thomas ; Bhogaraju, Sagar ; Noh, Kyung-Min ; Savitski, Mikhail ; Mahamid, Julia ; Hennig, Janosch:
TRIM2 E3 ligase substrate discovery reveals zinc-mediated regulation of TMEM106B in the endolysosomal pathway.
In: EMBO Reports. (2026) .
ISSN 1469-3178
DOI: https://doi.org/10.1038/s44319-025-00667-3

Project information

Abstract in another language

TRIM2 is a mammalian E3 ligase with particularly high expression in Purkinje neurons, where it contributes to neuronal development and homeostasis. The understanding of ubiquitin E3 ligase function hinges on thoroughly identifying their cellular targets, but the transient nature of signaling complexes leading to ubiquitination poses a significant challenge for detailed mechanistic studies. Here, we tailored a recently developed ubiquitin-specific proximity labeling tool to identify substrates of TRIM2 in cells. We show that TRIM2 targets proteins involved in the endolysosomal pathway. Specifically, we demonstrate using biochemical and structural studies, that TRIM2 ubiquitinates TMEM106B at lysine residues located in the cytosolic N-terminal region. Substrate recognition involves a direct interaction between TRIM2 and a newly identified zinc-coordination motif in TMEM106B that mediates homodimerization, is required for specific protein-protein interactions, and lysosomal size regulation. We found that in addition to catalysis, the tripartite motif is involved in substrate recruitment. Our study thus contributes a catalog of TRIM2 effectors and identifies a previously unrecognized regulatory region of TMEM106B crucial to its function.