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Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain
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 th...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089584/ https://www.ncbi.nlm.nih.gov/pubmed/27062398 http://dx.doi.org/10.1111/jnc.13636 |
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author | Kähne, Thilo Richter, Sandra Kolodziej, Angela Smalla, Karl‐Heinz Pielot, Rainer Engler, Alexander Ohl, Frank W. Dieterich, Daniela C. Seidenbecher, Constanze Tischmeyer, Wolfgang Naumann, Michael Gundelfinger, Eckart D. |
author_facet | Kähne, Thilo Richter, Sandra Kolodziej, Angela Smalla, Karl‐Heinz Pielot, Rainer Engler, Alexander Ohl, Frank W. Dieterich, Daniela C. Seidenbecher, Constanze Tischmeyer, Wolfgang Naumann, Michael Gundelfinger, Eckart D. |
author_sort | Kähne, Thilo |
collection | PubMed |
description | 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. [Image: see text]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. |
format | Online Article Text |
id | pubmed-5089584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50895842016-11-09 Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain Kähne, Thilo Richter, Sandra Kolodziej, Angela Smalla, Karl‐Heinz Pielot, Rainer Engler, Alexander Ohl, Frank W. Dieterich, Daniela C. Seidenbecher, Constanze Tischmeyer, Wolfgang Naumann, Michael Gundelfinger, Eckart D. J Neurochem ORIGINAL ARTICLES 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. [Image: see text]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. John Wiley and Sons Inc. 2016-05-26 2016-07 /pmc/articles/PMC5089584/ /pubmed/27062398 http://dx.doi.org/10.1111/jnc.13636 Text en © 2016 The Authors. Journal of Neurochemistry published by John Wiley & Sons Ltd on behalf of International Society for Neurochemistry. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | ORIGINAL ARTICLES Kähne, Thilo Richter, Sandra Kolodziej, Angela Smalla, Karl‐Heinz Pielot, Rainer Engler, Alexander Ohl, Frank W. Dieterich, Daniela C. Seidenbecher, Constanze Tischmeyer, Wolfgang Naumann, Michael Gundelfinger, Eckart D. Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain |
title | Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain |
title_full | Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain |
title_fullStr | Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain |
title_full_unstemmed | Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain |
title_short | Proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain |
title_sort | proteome rearrangements after auditory learning: high‐resolution profiling of synapse‐enriched protein fractions from mouse brain |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089584/ https://www.ncbi.nlm.nih.gov/pubmed/27062398 http://dx.doi.org/10.1111/jnc.13636 |
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