| First Author | Roppongi RT | Year | 2020 |
| Journal | Neuron | Volume | 106 |
| Issue | 1 | Pages | 108-125.e12 |
| PubMed ID | 31995730 | Mgi Jnum | J:292715 |
| Mgi Id | MGI:6449295 | Doi | 10.1016/j.neuron.2020.01.003 |
| Citation | Roppongi RT, et al. (2020) LRRTMs Organize Synapses through Differential Engagement of Neurexin and PTPsigma. Neuron 106(1):108-125.e12 |
| abstractText | Presynaptic neurexins (Nrxs) and type IIa receptor-type protein tyrosine phosphatases (RPTPs) organize synapses through a network of postsynaptic ligands. We show that leucine-rich-repeat transmembrane neuronal proteins (LRRTMs) differentially engage the protein domains of Nrx but require its heparan sulfate (HS) modification to induce presynaptic differentiation. Binding to the HS of Nrx is sufficient for LRRTM3 and LRRTM4 to induce synaptogenesis. We identify mammalian Nrx1gamma as a potent synapse organizer and reveal LRRTM4 as its postsynaptic ligand. Mice expressing a mutant form of LRRTM4 that cannot bind to HS show structural and functional deficits at dentate gyrus excitatory synapses. Through the HS of Nrx, LRRTMs also recruit PTPsigma to induce presynaptic differentiation but function to varying degrees in its absence. PTPsigma forms a robust complex with Nrx, revealing an unexpected interaction between the two presynaptic hubs. These findings underscore the complex interplay of synapse organizers in specifying the molecular logic of a neural circuit. |
