| Literature DB >> 7736595 |
K Ichtchenko1, Y Hata, T Nguyen, B Ullrich, M Missler, C Moomaw, T C Südhof.
Abstract
Neurexins are neuronal cell surface proteins with hundreds of isoforms generated by alternative splicing. Here we describe neuroligin 1, a neuronal cell surface protein that is enriched in synaptic plasma membranes and acts as a splice site-specific ligand for beta-neurexins. Neuroligin 1 binds to beta-neurexins only if they lack an insert in the alternatively spliced sequence of the G domain, but not if they contain an insert. The extracellular sequence of neuroligin 1 is composed of a catalytically inactive esterase domain homologous to acetylcholinesterase. In situ hybridization reveals that alternative splicing of neurexins at the site recognized by neuroligin 1 is highly regulated. These findings support a model whereby alternative splicing of neurexins creates a family of cell surface receptors that confers interactive specificity onto their resident neurons.Entities:
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Year: 1995 PMID: 7736595 DOI: 10.1016/0092-8674(95)90396-8
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582