| First Author | Martenson JS | Year | 2017 |
| Journal | Elife | Volume | 6 |
| PubMed ID | 28816653 | Mgi Jnum | J:257148 |
| Mgi Id | MGI:6116938 | Doi | 10.7554/eLife.27443 |
| Citation | Martenson JS, et al. (2017) Assembly rules for GABAA receptor complexes in the brain. Elife 6:e27443 |
| abstractText | GABAA receptor (GABAAR) pentamers are assembled from a pool of 19 subunits, and variety in subunit combinations diversifies GABAAR functions to tune brain activity. Pentamers with distinct subunit compositions localize differentially at synaptic and non-synaptic sites to mediate phasic and tonic inhibition, respectively. Despite multitudes of theoretical permutations, limited subunit combinations have been identified in the brain. Currently, no molecular model exists for combinatorial GABAAR assembly in vivo. Here, we reveal assembly rules of native GABAAR complexes that explain GABAAR subunit subcellular distributions using mice and Xenopus laevis oocytes. First, alpha subunits possess intrinsic signals to segregate into distinct pentamers. Second, gamma2 is essential for GABAAR assembly with Neuroligin-2 (NL2) and GARLHs, which localize GABAARs at synapses. Third, delta suppresses alpha6 synaptic localization by preventing assembly with GARLHs/NL2. These findings establish the first molecular model for combinatorial GABAAR assembly in vivo and reveal an assembly pathway regulating GABAAR synaptic localization. |
