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Chronic exercise remodels the lysine acetylome in the mouse hippocampus

Physical exercise benefits hippocampal function through various molecular mechanisms. Protein acetylation, a conserved and widespread post-translational modification, is involved in the synaptic plasticity and memory. However, whether exercise can change global acetylation and the role of acetylated...

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Autores principales: Qian, Ping, Ma, Feifei, Zhang, Wanyu, Cao, Dingding, Li, Luya, Liu, Zhuo, Pei, Pei, Zhang, Ting, Wang, Shan, Wu, Jianxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650339/
https://www.ncbi.nlm.nih.gov/pubmed/36385767
http://dx.doi.org/10.3389/fnmol.2022.1023482
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author Qian, Ping
Ma, Feifei
Zhang, Wanyu
Cao, Dingding
Li, Luya
Liu, Zhuo
Pei, Pei
Zhang, Ting
Wang, Shan
Wu, Jianxin
author_facet Qian, Ping
Ma, Feifei
Zhang, Wanyu
Cao, Dingding
Li, Luya
Liu, Zhuo
Pei, Pei
Zhang, Ting
Wang, Shan
Wu, Jianxin
author_sort Qian, Ping
collection PubMed
description Physical exercise benefits hippocampal function through various molecular mechanisms. Protein acetylation, a conserved and widespread post-translational modification, is involved in the synaptic plasticity and memory. However, whether exercise can change global acetylation and the role of acetylated proteins in the hippocampus have remained largely unknown. Herein, using healthy adult mice running for 6 weeks as exercise model and sedentary mice as control, we analyzed the hippocampal lysine acetylome and proteome by Liquid chromatography-tandem mass spectrometry. As a result, we profiled the lysine acetylation landscape for the hippocampus and identified 3,876 acetyl sites and 1,764 acetylated proteins. A total of 272 acetyl sites on 252 proteins were differentially regulated by chronic exercise, among which 18.58% acetylated proteins were annotated in mitochondria. These proteins were dominantly deacetylated and mainly associated with carbon-related metabolism, the Hippo signaling pathway, ribosomes, and protein processing. Meanwhile, 21 proteins were significantly expressed and enriched in the pathway of complement and coagulation cascades. Our findings provide a new avenue for understanding the molecular mechanisms underlying the benefits of exercise for hippocampal function and can contribute to the promotion of public health.
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spelling pubmed-96503392022-11-15 Chronic exercise remodels the lysine acetylome in the mouse hippocampus Qian, Ping Ma, Feifei Zhang, Wanyu Cao, Dingding Li, Luya Liu, Zhuo Pei, Pei Zhang, Ting Wang, Shan Wu, Jianxin Front Mol Neurosci Neuroscience Physical exercise benefits hippocampal function through various molecular mechanisms. Protein acetylation, a conserved and widespread post-translational modification, is involved in the synaptic plasticity and memory. However, whether exercise can change global acetylation and the role of acetylated proteins in the hippocampus have remained largely unknown. Herein, using healthy adult mice running for 6 weeks as exercise model and sedentary mice as control, we analyzed the hippocampal lysine acetylome and proteome by Liquid chromatography-tandem mass spectrometry. As a result, we profiled the lysine acetylation landscape for the hippocampus and identified 3,876 acetyl sites and 1,764 acetylated proteins. A total of 272 acetyl sites on 252 proteins were differentially regulated by chronic exercise, among which 18.58% acetylated proteins were annotated in mitochondria. These proteins were dominantly deacetylated and mainly associated with carbon-related metabolism, the Hippo signaling pathway, ribosomes, and protein processing. Meanwhile, 21 proteins were significantly expressed and enriched in the pathway of complement and coagulation cascades. Our findings provide a new avenue for understanding the molecular mechanisms underlying the benefits of exercise for hippocampal function and can contribute to the promotion of public health. Frontiers Media S.A. 2022-10-28 /pmc/articles/PMC9650339/ /pubmed/36385767 http://dx.doi.org/10.3389/fnmol.2022.1023482 Text en Copyright © 2022 Qian, Ma, Zhang, Cao, Li, Liu, Pei, Zhang, Wang and Wu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Qian, Ping
Ma, Feifei
Zhang, Wanyu
Cao, Dingding
Li, Luya
Liu, Zhuo
Pei, Pei
Zhang, Ting
Wang, Shan
Wu, Jianxin
Chronic exercise remodels the lysine acetylome in the mouse hippocampus
title Chronic exercise remodels the lysine acetylome in the mouse hippocampus
title_full Chronic exercise remodels the lysine acetylome in the mouse hippocampus
title_fullStr Chronic exercise remodels the lysine acetylome in the mouse hippocampus
title_full_unstemmed Chronic exercise remodels the lysine acetylome in the mouse hippocampus
title_short Chronic exercise remodels the lysine acetylome in the mouse hippocampus
title_sort chronic exercise remodels the lysine acetylome in the mouse hippocampus
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650339/
https://www.ncbi.nlm.nih.gov/pubmed/36385767
http://dx.doi.org/10.3389/fnmol.2022.1023482
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