| First Author | Kim JY | Year | 2024 |
| Journal | Front Mol Neurosci | Volume | 17 |
| Pages | 1421932 | PubMed ID | 38932934 |
| Mgi Jnum | J:350269 | Mgi Id | MGI:7661579 |
| Doi | 10.3389/fnmol.2024.1421932 | Citation | Kim JY, et al. (2024) ARHGEF5 binds Drebrin and affects alpha-tubulin acetylation to direct neuronal morphogenesis and migration during mouse brain development. Front Mol Neurosci 17:1421932 |
| abstractText | Rho guanine nucleotide exchange factors (Rho GEFs) activate Rho GTPases, which act as molecular switches regulating various essential cellular functions. This study investigated the role of ARHGEF5, a Rho GEF known for its involvement in cell migration and invasion processes, in the context of brain development. We found that ARHGEF5 is essential for dendrite development during the early stages of neuronal growth. We also discovered that ARHGEF5 binds to Drebrin E, which is vital for coordinating actin and microtubule dynamics, and facilitates the interaction between Drebrin E and Cyclin-dependent kinase 5, which phosphorylates Drebrin E. Notably, ARHGEF5 deficiency resulted in a decrease in acetylated alpha-tubulin levels, and the expression of an alpha-tubulin acetylation mimetic mutant (K40Q) rescued the defects in dendrite development and neuronal migration, suggesting ARHGEF5's role in modulating microtubule stability. Additionally, ARHGEF5 was shown to influence Golgi positioning in the leading processes of migrating cortical neurons during brain development. Our study suggests that ARHGEF5 plays a crucial role in integrating cytoskeletal dynamics with neuronal morphogenesis and migration processes during brain development. |
