Cargando…
In-depth proteome analysis of brain tissue from Ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling
EWS RNA binding protein 1 (EWSR1) is a multifunctional protein whose epigenetic signatures contribute to the pathogenesis of various human diseases, such as neurodegenerative disorders, skin development, and tumorigenic processes. However, the specific cellular functions and physiological characteri...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502055/ https://www.ncbi.nlm.nih.gov/pubmed/37709831 http://dx.doi.org/10.1038/s41598-023-42161-7 |
_version_ | 1785106236307406848 |
---|---|
author | Jung, Jin Woo Kim, Hyeyoon Park, Joonho Woo, Jongmin Jeon, Eunji Lee, Geeeun Park, Minseo Kim, Sarang Seo, Hoseok Cheon, Seongmin Dan, Kisoon Lee, Junghee Ryu, Hoon Han, Dohyun |
author_facet | Jung, Jin Woo Kim, Hyeyoon Park, Joonho Woo, Jongmin Jeon, Eunji Lee, Geeeun Park, Minseo Kim, Sarang Seo, Hoseok Cheon, Seongmin Dan, Kisoon Lee, Junghee Ryu, Hoon Han, Dohyun |
author_sort | Jung, Jin Woo |
collection | PubMed |
description | EWS RNA binding protein 1 (EWSR1) is a multifunctional protein whose epigenetic signatures contribute to the pathogenesis of various human diseases, such as neurodegenerative disorders, skin development, and tumorigenic processes. However, the specific cellular functions and physiological characteristics of EWSR1 remain unclear. In this study, we used quantitative mass spectrometry-based proteomics with tandem mass tag labeling to investigate the global proteome changes in brain tissue in Ewsr1 knockout and wild-type mice. From 9115 identified proteins, we selected 118 differentially expressed proteins, which is common to three quantitative data processing strategies including only protein level normalizations and spectrum-protein level normalization. Bioinformatics analysis of these common differentially expressed proteins revealed that proteins up-regulated in Ewsr1 knockout mouse are mostly related to the positive regulation of bone remodeling and inflammatory response. The down-regulated proteins were associated with the regulation of neurotransmitter levels or amino acid metabolic processes. Collectively, these findings provide insight into the physiological function and pathogenesis of EWSR1 on protein level. Better understanding of EWSR1 and its protein interactions will advance the field of clinical research into neuronal disorders. The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD026994. |
format | Online Article Text |
id | pubmed-10502055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105020552023-09-16 In-depth proteome analysis of brain tissue from Ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling Jung, Jin Woo Kim, Hyeyoon Park, Joonho Woo, Jongmin Jeon, Eunji Lee, Geeeun Park, Minseo Kim, Sarang Seo, Hoseok Cheon, Seongmin Dan, Kisoon Lee, Junghee Ryu, Hoon Han, Dohyun Sci Rep Article EWS RNA binding protein 1 (EWSR1) is a multifunctional protein whose epigenetic signatures contribute to the pathogenesis of various human diseases, such as neurodegenerative disorders, skin development, and tumorigenic processes. However, the specific cellular functions and physiological characteristics of EWSR1 remain unclear. In this study, we used quantitative mass spectrometry-based proteomics with tandem mass tag labeling to investigate the global proteome changes in brain tissue in Ewsr1 knockout and wild-type mice. From 9115 identified proteins, we selected 118 differentially expressed proteins, which is common to three quantitative data processing strategies including only protein level normalizations and spectrum-protein level normalization. Bioinformatics analysis of these common differentially expressed proteins revealed that proteins up-regulated in Ewsr1 knockout mouse are mostly related to the positive regulation of bone remodeling and inflammatory response. The down-regulated proteins were associated with the regulation of neurotransmitter levels or amino acid metabolic processes. Collectively, these findings provide insight into the physiological function and pathogenesis of EWSR1 on protein level. Better understanding of EWSR1 and its protein interactions will advance the field of clinical research into neuronal disorders. The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD026994. Nature Publishing Group UK 2023-09-14 /pmc/articles/PMC10502055/ /pubmed/37709831 http://dx.doi.org/10.1038/s41598-023-42161-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jung, Jin Woo Kim, Hyeyoon Park, Joonho Woo, Jongmin Jeon, Eunji Lee, Geeeun Park, Minseo Kim, Sarang Seo, Hoseok Cheon, Seongmin Dan, Kisoon Lee, Junghee Ryu, Hoon Han, Dohyun In-depth proteome analysis of brain tissue from Ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling |
title | In-depth proteome analysis of brain tissue from Ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling |
title_full | In-depth proteome analysis of brain tissue from Ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling |
title_fullStr | In-depth proteome analysis of brain tissue from Ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling |
title_full_unstemmed | In-depth proteome analysis of brain tissue from Ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling |
title_short | In-depth proteome analysis of brain tissue from Ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling |
title_sort | in-depth proteome analysis of brain tissue from ewsr1 knockout mouse by multiplexed isobaric tandem mass tag labeling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502055/ https://www.ncbi.nlm.nih.gov/pubmed/37709831 http://dx.doi.org/10.1038/s41598-023-42161-7 |
work_keys_str_mv | AT jungjinwoo indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT kimhyeyoon indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT parkjoonho indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT woojongmin indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT jeoneunji indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT leegeeeun indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT parkminseo indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT kimsarang indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT seohoseok indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT cheonseongmin indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT dankisoon indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT leejunghee indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT ryuhoon indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling AT handohyun indepthproteomeanalysisofbraintissuefromewsr1knockoutmousebymultiplexedisobarictandemmasstaglabeling |