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自我回避的分子基础。

The molecular basis of self-avoidance.

机构信息

Department of Biological Chemistry, Howard Hughes Medical Institute, David Geffen School of Medicine, University of California-Los Angeles, CA 90095-1662, USA.

出版信息

Annu Rev Neurosci. 2013 Jul 8;36:547-68. doi: 10.1146/annurev-neuro-062111-150414.

Abstract

Self-avoidance, the tendency of neurites of the same cell to selectively avoid each other, is a property of both vertebrate and invertebrate neurons. In Drosophila, self-avoidance is mediated by a large family of cell recognition molecules of the immunoglobulin superfamily encoded, via alternative splicing, by the Dscam1 locus. Dscam1 promotes self-avoidance in dendrites, axons, and prospective postsynaptic elements. Expression analysis suggests that each neuron expresses a unique combination of isoforms. Identical isoforms on sister neurites exhibit isoform-specific homophilic recognition and elicit repulsion between processes, thereby promoting self-avoidance. Although any isoform can promote self-avoidance, thousands are necessary to ensure that neurites readily discriminate between self and nonself. Recent studies indicate that a large family of cadherins in the mouse, i.e., the clustered protocadherins, functions in an analogous fashion to promote self-avoidance. These studies argue for the evolution of a common molecular strategy for self-avoidance.

摘要

自我回避,即同一细胞的神经突选择性地相互回避的趋势,是脊椎动物和无脊椎动物神经元的共同特性。在果蝇中,自我回避是由一个庞大的免疫球蛋白超家族的细胞识别分子家族介导的,这些分子通过选择性剪接,由 Dscam1 基因座编码。Dscam1 促进树突、轴突和潜在的突触后成分的自我回避。表达分析表明,每个神经元表达的异构体组合都是独特的。姐妹神经突上相同的异构体表现出异构体特异性的同种型识别,并在过程之间引起排斥,从而促进自我回避。尽管任何异构体都可以促进自我回避,但需要数千个异构体来确保神经突能够轻易地区分自我和非自我。最近的研究表明,小鼠中一大类钙粘蛋白,即簇状原钙粘蛋白,以类似的方式发挥作用,以促进自我回避。这些研究证明了自我回避的共同分子策略的进化。

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