A TBK1-independent primordial function of STING in lysosomal biogenesis

• DOI: 10.1016/j.molcel.2024.08.026
• Publication Date: 2024-09-19T15:55:00Z
• Authors: Bo Lv; William A. Dion; Haoxiang Yang; Jinrui Xun; Do-Hyung Kim; Bokai Zhu; Jay Xiaojun Tan
• Keywords: Mice, Knockout; Mice; HEK293 Cells; Organelle Biogenesis; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Cell Survival; Autophagy; Animals; Membrane Proteins; Humans; Protein Serine-Threonine Kinases; Lysosomes; Signal Transduction

Stimulator of interferon genes (STING) is activated in many pathophysiological conditions, leading to TBK1-dependent interferon production in higher organisms. However, primordial functions of STING independent of TBK1 are poorly understood. Here, through proteomics and bioinformatics approaches, we identify lysosomal biogenesis as an unexpected function of STING. Transcription factor EB (TFEB), an evolutionarily conserved regulator of lysosomal biogenesis and host defense, is activated by STING from multiple species, including humans, mice, and frogs. STING-mediated TFEB activation is independent of TBK1, but it requires STING trafficking and its conserved proton channel. GABARAP lipidation, stimulated by the channel of STING, is key for STING-dependent TFEB activation. STING stimulates global upregulation of TFEB-target genes, mediating lysosomal biogenesis and autophagy. TFEB supports cell survival during chronic sterile STING activation, a common condition in aging and age-related diseases. These results reveal a primordial function of STING in the biogenesis of lysosomes, essential organelles in immunity and cellular stress resistance.