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Proteome dynamics during postnatal mouse corpus callosum development

Formation of cortical connections requires the precise coordination of numerous discrete phases. This is particularly significant with regard to the corpus callosum, whose development undergoes several dynamic stages including the crossing of axon projections, elimination of exuberant projections, a...

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Autores principales: Son, Alexander I., Fu, Xiaoqin, Suto, Fumikazu, Liu, Judy S., Hashimoto-Torii, Kazue, Torii, Masaaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368975/
https://www.ncbi.nlm.nih.gov/pubmed/28349996
http://dx.doi.org/10.1038/srep45359
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author Son, Alexander I.
Fu, Xiaoqin
Suto, Fumikazu
Liu, Judy S.
Hashimoto-Torii, Kazue
Torii, Masaaki
author_facet Son, Alexander I.
Fu, Xiaoqin
Suto, Fumikazu
Liu, Judy S.
Hashimoto-Torii, Kazue
Torii, Masaaki
author_sort Son, Alexander I.
collection PubMed
description Formation of cortical connections requires the precise coordination of numerous discrete phases. This is particularly significant with regard to the corpus callosum, whose development undergoes several dynamic stages including the crossing of axon projections, elimination of exuberant projections, and myelination of established tracts. To comprehensively characterize the molecular events in this dynamic process, we set to determine the distinct temporal expression of proteins regulating the formation of the corpus callosum and their respective developmental functions. Mass spectrometry-based proteomic profiling was performed on early postnatal mouse corpus callosi, for which limited evidence has been obtained previously, using stable isotope of labeled amino acids in mammals (SILAM). The analyzed corpus callosi had distinct proteomic profiles depending on age, indicating rapid progression of specific molecular events during this period. The proteomic profiles were then segregated into five separate clusters, each with distinct trajectories relevant to their intended developmental functions. Our analysis both confirms many previously-identified proteins in aspects of corpus callosum development, and identifies new candidates in understudied areas of development including callosal axon refinement. We present a valuable resource for identifying new proteins integral to corpus callosum development that will provide new insights into the development and diseases afflicting this structure.
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spelling pubmed-53689752017-03-30 Proteome dynamics during postnatal mouse corpus callosum development Son, Alexander I. Fu, Xiaoqin Suto, Fumikazu Liu, Judy S. Hashimoto-Torii, Kazue Torii, Masaaki Sci Rep Article Formation of cortical connections requires the precise coordination of numerous discrete phases. This is particularly significant with regard to the corpus callosum, whose development undergoes several dynamic stages including the crossing of axon projections, elimination of exuberant projections, and myelination of established tracts. To comprehensively characterize the molecular events in this dynamic process, we set to determine the distinct temporal expression of proteins regulating the formation of the corpus callosum and their respective developmental functions. Mass spectrometry-based proteomic profiling was performed on early postnatal mouse corpus callosi, for which limited evidence has been obtained previously, using stable isotope of labeled amino acids in mammals (SILAM). The analyzed corpus callosi had distinct proteomic profiles depending on age, indicating rapid progression of specific molecular events during this period. The proteomic profiles were then segregated into five separate clusters, each with distinct trajectories relevant to their intended developmental functions. Our analysis both confirms many previously-identified proteins in aspects of corpus callosum development, and identifies new candidates in understudied areas of development including callosal axon refinement. We present a valuable resource for identifying new proteins integral to corpus callosum development that will provide new insights into the development and diseases afflicting this structure. Nature Publishing Group 2017-03-28 /pmc/articles/PMC5368975/ /pubmed/28349996 http://dx.doi.org/10.1038/srep45359 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Son, Alexander I.
Fu, Xiaoqin
Suto, Fumikazu
Liu, Judy S.
Hashimoto-Torii, Kazue
Torii, Masaaki
Proteome dynamics during postnatal mouse corpus callosum development
title Proteome dynamics during postnatal mouse corpus callosum development
title_full Proteome dynamics during postnatal mouse corpus callosum development
title_fullStr Proteome dynamics during postnatal mouse corpus callosum development
title_full_unstemmed Proteome dynamics during postnatal mouse corpus callosum development
title_short Proteome dynamics during postnatal mouse corpus callosum development
title_sort proteome dynamics during postnatal mouse corpus callosum development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368975/
https://www.ncbi.nlm.nih.gov/pubmed/28349996
http://dx.doi.org/10.1038/srep45359
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