| First Author | Wu Z | Year | 2023 |
| Journal | EMBO Rep | Volume | 24 |
| Issue | 5 | Pages | e55641 |
| PubMed ID | 36929224 | Mgi Jnum | J:336764 |
| Mgi Id | MGI:7470655 | Doi | 10.15252/embr.202255641 |
| Citation | Wu Z, et al. (2023) FAM69C functions as a kinase for eIF2alpha and promotes stress granule assembly. EMBO Rep 24(5):e55641 |
| abstractText | Stress granules are dynamic cytoplasmic ribonucleoprotein granules that assemble in response to cellular stress. Aberrant formation of stress granules has been linked to neurodegenerative diseases. However, the molecular mechanisms underlying the initiation of stress granules remain elusive. Here we report that the brain-enriched protein kinase FAM69C promotes stress granule assembly through phosphorylation of eukaryotic translation initiation factor 2 (eIF2alpha). FAM69C physically interacts with eIF2alpha and functions as a stress-specific kinase for eIF2alpha, leading to stress-induced protein translation arrest and stress granule assembly. Primary microglia derived from Fam69c knockout mice exhibit aberrant stress granule assembly in response to oxidative stress and ATP. Defective stress granule assembly in microglia correlates with the formation of ASC specks and NLRP3 inflammasome activation, whereas induction of stress granule precludes inflammasome formation. Consistently, increased NLRP3 levels, caspase-1 cleavage and Il18 expression corroborate microglia-associated neuroinflammation in aged Fam69c knockout mice. Our study demonstrates that FAM69C is critical for stress granule assembly and suggests its role in the regulation of microglia function. |
