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Synaptic proteome changes in mouse brain regions upon auditory discrimination learning
Author(s) -
Kähne Thilo,
Kolodziej Angela,
Smalla KarlHeinz,
Eisenschmidt Elke,
Haus UtzUwe,
Weismantel Robert,
Kropf Siegfried,
Wetzel Wolfram,
Ohl Frank W.,
Tischmeyer Wolfgang,
Naumann Michael,
Gundelfinger Eckart D.
Publication year - 2012
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.201100669
Subject(s) - proteome , neuroscience , postsynaptic potential , hippocampus , biology , auditory cortex , postsynaptic density , striatum , biochemistry , receptor , dopamine
Changes in synaptic efficacy underlying learning and memory processes are assumed to be associated with alterations of the protein composition of synapses. Here, we performed a quantitative proteomic screen to monitor changes in the synaptic proteome of four brain areas (auditory cortex, frontal cortex, hippocampus striatum) during auditory learning. Mice were trained in a shuttle box GO / NO ‐ GO paradigm to discriminate between rising and falling frequency modulated tones to avoid mild electric foot shock. Control‐treated mice received corresponding numbers of either the tones or the foot shocks. Six hours and 24 h later, the composition of a fraction enriched in synaptic cytomatrix‐associated proteins was compared to that obtained from naïve mice by quantitative mass spectrometry. In the synaptic protein fraction obtained from trained mice, the average percentage (± SEM ) of downregulated proteins (59.9 ± 0.5%) exceeded that of upregulated proteins (23.5 ± 0.8%) in the brain regions studied. This effect was significantly smaller in foot shock (42.7 ± 0.6% down, 40.7 ± 1.0% up) and tone controls (43.9 ± 1.0% down, 39.7 ± 0.9% up). These data suggest that learning processes initially induce removal and/or degradation of proteins from presynaptic and postsynaptic cytoskeletal matrices before these structures can acquire a new, postlearning organisation. In silico analysis points to a general role of insulin‐like signalling in this process.