首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain
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Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain

机译:听觉学习后的蛋白质组重排:小鼠脑中富含突触的蛋白质部分的高分辨率分析

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摘要

Learning and memory processes are accompanied by rearrangements of synaptic protein networks. While various studies have demonstrated the regulation of individual synaptic proteins during these processes, much less is known about the complex regulation of synaptic proteomes. Recently, we reported that auditory discrimination learning in mice is associated with a relative down‐regulation of proteins involved in the structural organization of synapses in various brain regions. Aiming at the identification of biological processes and signaling pathways involved in auditory memory formation, here, a label‐free quantification approach was utilized to identify regulated synaptic junctional proteins and phosphoproteins in the auditory cortex, frontal cortex, hippocampus, and striatum of mice 24 h after the learning experiment. Twenty proteins, including postsynaptic scaffolds, actin‐remodeling proteins, and RNA‐binding proteins, were regulated in at least three brain regions pointing to common, cross‐regional mechanisms. Most of the detected synaptic proteome changes were, however, restricted to individual brain regions. For example, several members of the Septin family of cytoskeletal proteins were up‐regulated only in the hippocampus, while Septin‐9 was down‐regulated in the hippocampus, the frontal cortex, and the striatum. Meta analyses utilizing several databases were employed to identify underlying cellular functions and biological pathways. Data are available via ProteomeExchange with identifier PXD003089.
机译:学习和记忆过程伴随着突触蛋白网络的重排。尽管各种研究已经证明了在这些过程中单个突触蛋白的调控,但对突触蛋白组学的复杂调控知之甚少。最近,我们报道了小鼠的听觉歧视学习与大脑各个区域的突触结构组织中涉及的蛋白质相对下调有关。为了识别与听觉记忆形成有关的生物学过程和信号传导途径,此处采用了无标记的定量方法来鉴定小鼠听觉皮层,额叶皮层,海马和纹状体中受调节的突触结合蛋白和磷酸化蛋白24小时经过学习实验。至少在三个指向共同的跨区域机制的大脑区域中,对二十种蛋白质进行了调节,其中包括突触后支架,肌动蛋白重塑蛋白和RNA结合蛋白。然而,大多数检测到的突触蛋白质组变化仅限于单个大脑区域。例如,Septin细胞骨架蛋白家族的几个成员仅在海马中被上调,而Septin-9在海马,额叶皮层和纹状体中被下调。利用利用几个数据库的元分析来识别潜在的细胞功能和生物学途径。数据可通过ProteomeExchange获得,标识符为PXD003089。

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