The LRR and RING domain protein LRSAM1 is an E3 ligase crucial for ubiquitin-dependent autophagy of intracellular salmonella typhimurium

Huett, Alan; Heath, Robert J.; Begun, Jakob; Sassi, Slim O.; Baxt, Leigh A.; Vyas, Jatin M.; Goldberg, Marcia B.; Xavier, Ramnik J.

Abstract

Several species of pathogenic bacteria replicate within an intracellular vacuolar niche. Bacteria that escape into the cytosol are captured by the autophagic pathway and targeted for lysosomal degradation, representing a defense against bacterial exploitation of the host cytosol. Autophagic capture of Salmonella Typhimurium occurs predominantly via generation of a polyubiquitin signal around cytosolic bacteria, binding of adaptor proteins, and recruitment of autophagic machinery. However, the components mediating bacterial target selection and ubiquitination remain obscure. We identify LRSAM1 as the E3 ligase responsible for anti-Salmonella autophagy-associated ubiquitination. LRSAM1 localizes to several intracellular bacterial pathogens and generates the bacteria-associated ubiquitin signal; these functions require LRSAM1's leucine-rich repeat and RING domains, respectively. Using cells from LRSAM1-deficient individuals, we confirm that LRSAM1 is required for ubiquitination associated with intracellular bacteria but dispensable for ubiquitination of aggregated proteins. LRSAM1 is therefore a bacterial recognition protein and ubiquitin ligase that defends the cytoplasm from invasive pathogens. © 2012 Elsevier Inc.

Citation

Huett, A., Heath, R. J., Begun, J., Sassi, S. O., Baxt, L. A., Vyas, J. M., Goldberg, M. B., & Xavier, R. J. (2012). The LRR and RING domain protein LRSAM1 is an E3 ligase crucial for ubiquitin-dependent autophagy of intracellular salmonella typhimurium. Cell Host and Microbe, 12(6), 778-790. https://doi.org/10.1016/j.chom.2012.10.019

• Journal Article Type: Article
• Acceptance Date: Oct 30, 2012
• Online Publication Date: Dec 12, 2012
• Publication Date: Dec 13, 2012
• Deposit Date: Aug 15, 2022
• Journal: Cell Host and Microbe
• Print ISSN: 1931-3128
• Electronic ISSN: 1934-6069
• Publisher: Cell Press
• Peer Reviewed: Peer Reviewed
• Volume: 12
• Issue: 6
• Pages: 778-790
• DOI: https://doi.org/10.1016/j.chom.2012.10.019
• Public URL: https://nottingham-repository.worktribe.com/output/3181758
• Publisher URL: https://www.sciencedirect.com/science/article/pii/S1931312812003915?via%3Dihub