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缺乏突触蛋白 SAP47 会损害行为和突触可塑性。

Behavioral and synaptic plasticity are impaired upon lack of the synaptic protein SAP47.

机构信息

Neurobiologie und Genetik and Elektronenmikroskopie, Universität Würzburg, Biozentrum, 97074 Würzburg, Germany.

出版信息

J Neurosci. 2011 Mar 2;31(9):3508-18. doi: 10.1523/JNEUROSCI.2646-10.2011.

Abstract

The synapse-associated protein of 47 kDa (SAP47) is a member of a phylogenetically conserved gene family of hitherto unknown function. In Drosophila, SAP47 is encoded by a single gene (Sap47) and is expressed throughout all synaptic regions of the wild-type larval brain; specifically, electron microscopy reveals anti-SAP47 immunogold labeling within 30 nm of presynaptic vesicles. To analyze SAP47 function, we used the viable and fertile deletion mutant Sap47(156), which suffers from a 1.7 kb deletion in the regulatory region and the first exon. SAP47 cannot be detected by either immunoblotting or immunohistochemistry in Sap47(156) mutants. These mutants exhibit normal sensory detection of odorants and tastants as well as normal motor performance and basic neurotransmission at the neuromuscular junction. However, short-term plasticity at this synapse is distorted. Interestingly, Sap47(156) mutant larvae also show a 50% reduction in odorant-tastant associative learning ability; a similar associative impairment is observed in a second deletion allele (Sap47(201)) and upon reduction of SAP47 levels using RNA interference. In turn, transgenically restoring SAP47 in Sap47(156) mutant larvae rescues the defect in associative function. This report thus is the first to suggest a function for SAP47. It specifically argues that SAP47 is required for proper behavioral and synaptic plasticity in flies-and prompts the question whether its homologs are required for proper behavioral and synaptic plasticity in other species as well.

摘要

突触相关蛋白 47kDa(SAP47)是一个具有未知功能的进化保守基因家族的成员。在果蝇中,SAP47 由一个单一基因(Sap47)编码,在野生型幼虫大脑的所有突触区域都有表达;具体来说,电镜显示抗 SAP47 免疫金标记位于突触小泡 30nm 内。为了分析 SAP47 的功能,我们使用了具有活力和可育的缺失突变体 Sap47(156),该突变体在调节区和第一个外显子中发生了 1.7kb 的缺失。在 Sap47(156)突变体中,无论是免疫印迹还是免疫组织化学都无法检测到 SAP47。这些突变体在嗅觉和味觉的感觉检测、运动表现以及神经肌肉接头的基本神经传递方面都正常。然而,这个突触的短期可塑性受到了扭曲。有趣的是,Sap47(156)突变体幼虫的嗅觉-味觉联想学习能力也降低了 50%;在第二个缺失等位基因(Sap47(201))和使用 RNA 干扰降低 SAP47 水平时,也观察到类似的联想损伤。反过来,在 Sap47(156)突变体幼虫中转基因恢复 SAP47 可挽救联想功能的缺陷。因此,本报告首次提出了 SAP47 的功能。它特别表明,SAP47 是果蝇正常行为和突触可塑性所必需的,这也引发了一个问题,即它的同源物是否也是其他物种正常行为和突触可塑性所必需的。

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