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神经连接蛋白1:β-神经突触素的一个剪接位点特异性配体。

Neuroligin 1: a splice site-specific ligand for beta-neurexins.

作者信息

Ichtchenko K, Hata Y, Nguyen T, Ullrich B, Missler M, Moomaw C, Südhof T C

机构信息

Department of Molecular Genetics, University of Texas Southwestern Medical Center at Dallas 75235, USA.

出版信息

Cell. 1995 May 5;81(3):435-43. doi: 10.1016/0092-8674(95)90396-8.

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.

摘要

神经连接蛋白是神经元细胞表面蛋白,通过可变剪接产生数百种异构体。在这里,我们描述了neuroligin 1,一种在突触质膜中富集的神经元细胞表面蛋白,它作为β-神经连接蛋白的剪接位点特异性配体。只有当β-神经连接蛋白在G结构域的可变剪接序列中没有插入片段时,neuroligin 1才会与之结合,而当它们含有插入片段时则不会。neuroligin 1的细胞外序列由与乙酰胆碱酯酶同源的无催化活性的酯酶结构域组成。原位杂交显示,在neuroligin 1识别的位点上,神经连接蛋白的可变剪接受严格调控。这些发现支持了一个模型,即神经连接蛋白的可变剪接产生了一系列细胞表面受体,赋予其所在神经元相互作用特异性。

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