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Molecular and Genetic Analysis of Synaptic Signaling in Drosophila

机译:果蝇突触信号的分子和遗传分析。

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摘要

Molecular and genetic analysis of synaptic signaling in Drosophila has yielded many insights into nervous system development, properties of synaptic transmission, and how long-lasting changes in neurons occur. Synaptic signaling components required for synaptic transmission and pathways leading to nervous system plasticity are typically conserved from insects to humans. The role of proteins and genes in synaptic function in flies can be analyzed from the level of a single synapse to complex behaviors in the whole organism. Because of a fully sequenced genome and the ease of mutagenesis in flies, genetic screens have been useful in identifying novel regulators of synaptic transmission and long-term memory.In flies, conditional mutations affecting synaptic transmission at nerve terminals often lead to temperature sensitive paralysis. In a screen for mutations that interact with Drosophila shibirets mutants, the stoned gene was identified as a regulator of synaptic vesicle cycling. Stoned encodes two neuronally expressed proteins, stonedA and B, which are required for synaptic vesicle recycling and normal synaptic transmission. However, the exact functions of the two stoned proteins are not fully understood. We investigate distinct roles of the stoned proteins here and show that stoned has a novel role in synaptic growth.Memory in flies can be divided into genetically distinct phases based on the requirement for protein synthesis and activation of the transcription factor CREB. Novel regulators of long-term olfactory avoidance memory were isolated in a mutant screen in flies. Mutants in the Drosophila gene lk6, homologous to the translational regulator MNK, have defects in long-term olfactory avoidance memory. We find that lk6 is highly expressed in the fly nervous system, and is activated by and functions downstream of Ras/ERK signaling in fly neurons. Insights provided here from Drosophila add to the evidence that MNK may be the link between ERK signaling and the regulation of translation in long-term plasticity.Ultimately, understanding synaptic function has therapeutic potential to aid in alleviation of nervous system dysfunction. Insight into the molecular pathways underlying plasticity and long-term memory gained from studies in flies, mollusks, and rodents has been pivotal in the development of potential drugs to aid in memory deficits in humans.
机译:果蝇中突触信号传导的分子和遗传分析已对神经系统发育,突触传递特性以及神经元如何持续发生变化产生了许多见解。突触传递和导致神经系统可塑性的途径所需的突触信号成分通常从昆虫到人类都是保守的。蛋白质和基因在果蝇突触功能中的作用可以从单个突触的水平到整个生物体的复杂行为进行分析。由于基因组的序列已完全测序,并且苍蝇易于诱变,因此遗传筛选可用于识别新型的突触传递和长期记忆调节剂。在苍蝇中,影响神经末梢突触传递的条件突变通常会导致温度敏感性麻痹。在筛选与果蝇Shibirets突变体相互作用的突变时,被鉴定的基因被确定为突触小泡循环的调节剂。 Stoned编码两种神经元表达的蛋白,stonedA和B,这是突触小泡再循环和正常突触传递所必需的。但是,这两种石头蛋白的确切功能尚不完全清楚。我们在这里研究了石头蛋白的独特作用,并表明石头蛋白在突触生长中具有新的作用。根据蛋白质合成和转录因子CREB激活的要求,果蝇的记忆可分为遗传上不同的阶段。在果蝇的突变体筛选中分离出了新型的长期嗅觉回避调节因子。果蝇基因lk6中的突变体,与翻译调节子MNK同源,在长期的嗅觉回避记忆中有缺陷。我们发现lk6在果蝇神经系统中高度表达,并由果蝇神经元中的Ras / ERK信号激活并在下游起作用。果蝇在这里提供的见解增加了证据,即MNK可能是ERK信号传导和长期可塑性翻译调控之间的联系。最终,了解突触功能具有治疗潜力,有助于缓解神经系统功能障碍。从果蝇,软体动物和啮齿类动物的研究中获得的对可塑性和长期记忆的分子途径的深入了解一直是开发潜在药物以帮助人类记忆不足的关键。

著录项

  • 作者

    Jackson Taryn;

  • 作者单位
  • 年度 2005
  • 总页数
  • 原文格式 PDF
  • 正文语种 EN
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