4.5 Article

Proteome rearrangements after auditory learning: high-resolution profiling of synapse-enriched protein fractions from mouse brain

期刊

JOURNAL OF NEUROCHEMISTRY
卷 138, 期 1, 页码 124-138

出版社

WILEY
DOI: 10.1111/jnc.13636

关键词

auditory learning; chemical synapse; label-free quantification; learning and memory; phosphoproteomics; quantitative mass spectrometry

资金

  1. Deutsche Forschungsgemeinschaft [SFB 779]
  2. State Saxony-Anhalt/European Regional Development Fund (ERDF) via the Center for Behavioral Brain Sciences (CBBS)
  3. Initiative for Research and Innovation of the Leibniz Association (SAW)

向作者/读者索取更多资源

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.

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