Suppr超能文献

细胞骨架调节因子成吉思汗在果蝇视觉系统的柱状靶标特异性中是必需的。

The cytoskeletal regulator Genghis khan is required for columnar target specificity in the Drosophila visual system.

机构信息

Department of Neurobiology, 299 W. Campus Drive, Stanford University, Stanford, CA 94305, USA.

出版信息

Development. 2011 Nov;138(22):4899-909. doi: 10.1242/dev.069930. Epub 2011 Oct 17.

Abstract

A defining characteristic of neuronal cell type is the growth of axons and dendrites into specific layers and columns of the brain. Although differences in cell surface receptors and adhesion molecules are known to cause differences in synaptic specificity, differences in downstream signaling mechanisms that determine cell type-appropriate targeting patterns are unknown. Using a forward genetic screen in Drosophila, we identify the GTPase effector Genghis khan (Gek) as playing a crucial role in the ability of a subset of photoreceptor (R cell) axons to innervate appropriate target columns. In particular, single-cell mosaic analyses demonstrate that R cell growth cones lacking Gek function grow to the appropriate ganglion, but frequently fail to innervate the correct target column. Further studies reveal that R cell axons lacking the activity of the small GTPase Cdc42 display similar defects, providing evidence that these proteins regulate a common set of processes. Gek is expressed in all R cells, and a detailed structure-function analysis reveals a set of regulatory domains with activities that restrict Gek function to the growth cone. Although Gek does not normally regulate layer-specific targeting, ectopic expression of Gek is sufficient to alter the targeting choices made by another R cell type, the targeting of which is normally Gek independent. Thus, specific regulation of cytoskeletal responses to targeting cues is necessary for cell type-appropriate synaptic specificity.

摘要

神经元细胞类型的一个特征是轴突和树突生长到大脑的特定层和柱中。虽然已知细胞表面受体和黏附分子的差异会导致突触特异性的差异,但决定细胞类型适当靶向模式的下游信号转导机制的差异尚不清楚。我们在果蝇中使用正向遗传筛选,确定 GTP 酶效应物 Genghis khan (Gek) 在一组光感受器 (R 细胞) 轴突能够支配适当的靶柱的能力中发挥关键作用。特别是,单细胞嵌合体分析表明,缺乏 Gek 功能的 R 细胞生长锥生长到适当的神经节,但经常不能支配正确的靶柱。进一步的研究表明,缺乏小 GTPase Cdc42 活性的 R 细胞轴突也显示出类似的缺陷,这提供了证据表明这些蛋白质调节一组共同的过程。Gek 在所有 R 细胞中表达,详细的结构-功能分析揭示了一组具有活性的调节域,这些活性将 Gek 功能限制在生长锥中。虽然 Gek 通常不调节层特异性靶向,但 Gek 的异位表达足以改变另一种 R 细胞类型的靶向选择,而这种靶向选择通常与 Gek 无关。因此,对靶向线索的细胞骨架反应的特定调节对于细胞类型适当的突触特异性是必要的。

相似文献

引用本文的文献

6
The cell biology of synaptic specificity during development.发育过程中突触特异性的细胞生物学。
Curr Opin Neurobiol. 2013 Dec;23(6):1018-26. doi: 10.1016/j.conb.2013.07.004. Epub 2013 Aug 6.

本文引用的文献

6
Many paths to synaptic specificity.多种途径实现突触特异性。
Annu Rev Cell Dev Biol. 2009;25:161-95. doi: 10.1146/annurev.cellbio.24.110707.175402.
7
Temporal identity in axonal target layer recognition.轴突靶层识别中的时间同一性
Nature. 2008 Dec 11;456(7223):800-3. doi: 10.1038/nature07407. Epub 2008 Nov 2.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验