NMDA受体的表达和C端结构在臂轮虫中的表达及后生动物的长时程增强。

Q4 Neuroscience Invertebrate Neuroscience Pub Date : 2013-12-01 Epub Date: 2013-04-02 DOI:10.1007/s10158-013-0154-0
Nathan J Kenny, Peter K Dearden
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引用次数: 2

摘要

n -甲基- d -天冬氨酸(NMDA)受体NR2亚基的C端被认为在通过被称为长期增强(LTP)的现象在双侧记忆的分子建立中起主要作用。尽管NR2亚基在记忆研究中被用作模型已有很长的历史,但其在磷藻类动物中的表达和结构仍未被分类。本文报道了NMDA NR1和NR2亚基在单纲轮虫臂轮虫(Brachionus plicatilis)中的克隆和原位表达分析。RNA原位杂交表明,NMDA受体亚基在B. plicatilis中的表达是神经的,与其他物种的表达一致,这是第一个证实NMDA受体亚基在光合动物分支中表达的报告。然而,在B. plicatilis中发现的单个NR2亚基缺乏脊椎动物中发现的长C末端结构域,这被认为是调节LTP的。进一步的研究发现,软体动物和环节动物的NR2亚基具有较长的胞内C端结构域。由于软体动物(尤其是加利福尼亚海陆动物)的数据是我们了解LTP的基础,了解这些不同的光栖动物C末端在体内的功能将对我们如何考虑整个后生动物学习和记忆的分子控制的进化以及将实验结果解释为认知的重要组成部分有许多影响。
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NMDA receptor expression and C terminus structure in the rotifer Brachionus plicatilis and long-term potentiation across the Metazoa.

The C termini of N-methyl-D-aspartate (NMDA) receptor NR2 subunits are thought to play a major role in the molecular establishment of memory across the Bilateria, via the phenomenon known as long-term potentiation (LTP). Despite their long history of use as models in the study of memory, the expression and structure of the NR2 subunit in the Lophotrochozoa has remained uncategorized. Here, we report the phylogenic relationships of NR subunits across the Bilateria, and the cloning and in situ analysis of expression of NMDA NR1 and NR2 subunits in the monogont rotifer Brachionus plicatilis. RNA in situ hybridization suggests expression of NMDA receptor subunits in B. plicatilis is neural, consistent with expression observed in other species, and ours is the first report confirming NR2 expression in the lophotrochozoan clade. However, the single NR2 subunit identified in B. plicatilis was found to lack the long C terminal domain found in vertebrates, which is believed to modulate LTP. Further investigation revealed that mollusc and annelid NR2 subunits possess long intracellular C terminal domains. As data from molluscs (and particularly Aplysia californica) are the basis for much of our understanding of LTP, understanding how these diverse lophotrochozoan C termini function in vivo will have many implications for how we consider the evolution of the molecular control of learning and memory across the Metazoa as a whole and interpret the results of experiments into this vital component of cognition.

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来源期刊
Invertebrate Neuroscience
Invertebrate Neuroscience NEUROSCIENCES-
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期刊介绍: Invertebrate Neurosciences publishes peer-reviewed original articles, reviews and technical reports describing recent advances in the field of invertebrate neuroscience. The journal reports on research that exploits the simplicity and experimental tractability of the invertebrate preparations to underpin fundamental advances in neuroscience. Articles published in Invertebrate Neurosciences serve to highlight properties of signalling in the invertebrate nervous system that may be exploited in the field of antiparisitics, molluscicides and insecticides. Aspects of particular interest include: Functional analysis of the invertebrate nervous system; Molecular neuropharmacology and toxicology; Neurogenetics and genomics; Functional anatomy; Neurodevelopment; Neuronal networks; Molecular and cellular mechanisms of behavior and behavioural plasticity.
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