Premium
Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain
Author(s) -
Kähne Thilo,
Richter Sandra,
Kolodziej Angela,
Smalla KarlHeinz,
Pielot Rainer,
Engler Alexander,
Ohl Frank W.,
Dieterich Daniela C.,
Seidenbecher Constanze,
Tischmeyer Wolfgang,
Naumann Michael,
Gundelfinger Eckart D.
Publication year - 2016
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/jnc.13636
Subject(s) - neuroscience , proteome , biology , striatum , synapse , hippocampus , auditory cortex , postsynaptic density , dopamine , bioinformatics , excitatory postsynaptic potential , inhibitory postsynaptic potential
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 PXD 003089.How does the protein composition of synapses change in different brain areas upon auditory learning? We unravel discrete proteome changes in mouse auditory cortex, frontal cortex, hippocampus, and striatum functionally implicated in the learning process. We identify not only common but also area‐specific biological pathways and cellular processes modulated 24 h after training, indicating individual contributions of the regions to memory processing.