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果蝇视觉图谱中突触伙伴的与活动无关的预先指定。

Activity-independent prespecification of synaptic partners in the visual map of Drosophila.

作者信息

Hiesinger P Robin, Zhai R Grace, Zhou Yi, Koh Tong-Wey, Mehta Sunil Q, Schulze Karen L, Cao Yu, Verstreken Patrik, Clandinin Thomas R, Fischbach Karl-Friedrich, Meinertzhagen Ian A, Bellen Hugo J

机构信息

Howard Hughes Medical Institute, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Curr Biol. 2006 Sep 19;16(18):1835-43. doi: 10.1016/j.cub.2006.07.047.

Abstract

Specifying synaptic partners and regulating synaptic numbers are at least partly activity-dependent processes during visual map formation in all systems investigated to date . In Drosophila, six photoreceptors that view the same point in visual space have to be sorted into synaptic modules called cartridges in order to form a visuotopically correct map . Synapse numbers per photoreceptor terminal and cartridge are both precisely regulated . However, it is unknown whether an activity-dependent mechanism or a genetically encoded developmental program regulates synapse numbers. We performed a large-scale quantitative ultrastructural analysis of photoreceptor synapses in mutants affecting the generation of electrical potentials (norpA, trp;trpl), neurotransmitter release (hdc, syt), vesicle endocytosis (synj), the trafficking of specific guidance molecules during photoreceptor targeting (sec15), a specific guidance receptor required for visual map formation (Dlar), and 57 other novel synaptic mutants affecting 43 genes. Remarkably, in all these mutants, individual photoreceptors form the correct number of synapses per presynaptic terminal independently of cartridge composition. Hence, our data show that each photoreceptor forms a precise and constant number of afferent synapses independently of neuronal activity and partner accuracy. Our data suggest cell-autonomous control of synapse numbers as part of a developmental program of activity-independent steps that lead to a "hard-wired" visual map in the fly brain.

摘要

在迄今为止所研究的所有系统中,在视觉图谱形成过程中,指定突触伙伴和调节突触数量至少部分是依赖于活动的过程。在果蝇中,观看视觉空间中同一点的六个光感受器必须被分类到称为小眼的突触模块中,以便形成视觉拓扑正确的图谱。每个光感受器终端和小眼的突触数量都受到精确调节。然而,尚不清楚是依赖活动的机制还是基因编码的发育程序调节突触数量。我们对影响电位产生(norpA、trp;trpl)、神经递质释放(hdc、syt)、囊泡内吞作用(synj)、光感受器靶向过程中特定导向分子的运输(sec15)、视觉图谱形成所需的特定导向受体(Dlar)以及影响43个基因的57个其他新型突触突变体中的光感受器突触进行了大规模定量超微结构分析。值得注意的是,在所有这些突变体中,单个光感受器每个突触前终端形成的突触数量正确,与小眼组成无关。因此,我们的数据表明,每个光感受器独立于神经元活动和伙伴准确性形成精确且恒定数量的传入突触。我们的数据表明,突触数量的细胞自主控制是导致果蝇大脑中“硬连线”视觉图谱的与活动无关步骤的发育程序的一部分。

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