| First Author | Fort L | Year | 2018 |
| Journal | Nat Cell Biol | Volume | 20 |
| Issue | 10 | Pages | 1159-1171 |
| PubMed ID | 30250061 | Mgi Jnum | J:268449 |
| Mgi Id | MGI:6270884 | Doi | 10.1038/s41556-018-0198-9 |
| Citation | Fort L, et al. (2018) Fam49/CYRI interacts with Rac1 and locally suppresses protrusions. Nat Cell Biol 20(10):1159-1171 |
| abstractText | Actin-based protrusions are reinforced through positive feedback, but it is unclear what restricts their size, or limits positive signals when they retract or split. We identify an evolutionarily conserved regulator of actin-based protrusion: CYRI (CYFIP-related Rac interactor) also known as Fam49 (family of unknown function 49). CYRI binds activated Rac1 via a domain of unknown function (DUF1394) shared with CYFIP, defining DUF1394 as a Rac1-binding module. CYRI-depleted cells have broad lamellipodia enriched in Scar/WAVE, but reduced protrusion-retraction dynamics. Pseudopods induced by optogenetic Rac1 activation in CYRI-depleted cells are larger and longer lived. Conversely, CYRI overexpression suppresses recruitment of active Scar/WAVE to the cell edge, resulting in short-lived, unproductive protrusions. CYRI thus focuses protrusion signals and regulates pseudopod complexity by inhibiting Scar/WAVE-induced actin polymerization. It thus behaves like a 'local inhibitor' as predicted in widely accepted mathematical models, but not previously identified in cells. CYRI therefore regulates chemotaxis, cell migration and epithelial polarization by controlling the polarity and plasticity of protrusions. |
