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Comparison of multi-tissue aging between human and mouse

With the rapid growth of the aging population, exploring the biological basis of aging and related molecular mechanisms has become an important topic in modern scientific research. Aging can cause multiple organ function attenuations, leading to the occurrence and development of various age-related...

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Autores principales: Zhuang, Jujuan, Zhang, Lijun, Dai, Shuang, Cui, Lingyu, Guo, Cheng, Sloofman, Laura, Yang, Jialiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470208/
https://www.ncbi.nlm.nih.gov/pubmed/30996271
http://dx.doi.org/10.1038/s41598-019-42485-3
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author Zhuang, Jujuan
Zhang, Lijun
Dai, Shuang
Cui, Lingyu
Guo, Cheng
Sloofman, Laura
Yang, Jialiang
author_facet Zhuang, Jujuan
Zhang, Lijun
Dai, Shuang
Cui, Lingyu
Guo, Cheng
Sloofman, Laura
Yang, Jialiang
author_sort Zhuang, Jujuan
collection PubMed
description With the rapid growth of the aging population, exploring the biological basis of aging and related molecular mechanisms has become an important topic in modern scientific research. Aging can cause multiple organ function attenuations, leading to the occurrence and development of various age-related metabolic, nervous system, and cardiovascular diseases. In addition, aging is closely related to the occurrence and development of tumors. Although a number of studies have used various mouse models to study aging, further research is needed to associate mouse and human aging at the molecular level. In this paper, we systematically assessed the relationship between human and mouse aging by comparing multi-tissue age-related gene expression sets. We compared 18 human and mouse tissues, and found 9 significantly correlated tissue pairs. Functional analysis also revealed some terms related to aging in human and mouse. And we performed a crosswise comparison of homologous age-related genes with 18 tissues in human and mouse respectively, and found that human Brain_Cortex was significantly correlated with Brain_Hippocampus, which was also found in mouse. In addition, we focused on comparing four brain-related tissues in human and mouse, and found a gene–GFAP–related to aging in both human and mouse.
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spelling pubmed-64702082019-04-25 Comparison of multi-tissue aging between human and mouse Zhuang, Jujuan Zhang, Lijun Dai, Shuang Cui, Lingyu Guo, Cheng Sloofman, Laura Yang, Jialiang Sci Rep Article With the rapid growth of the aging population, exploring the biological basis of aging and related molecular mechanisms has become an important topic in modern scientific research. Aging can cause multiple organ function attenuations, leading to the occurrence and development of various age-related metabolic, nervous system, and cardiovascular diseases. In addition, aging is closely related to the occurrence and development of tumors. Although a number of studies have used various mouse models to study aging, further research is needed to associate mouse and human aging at the molecular level. In this paper, we systematically assessed the relationship between human and mouse aging by comparing multi-tissue age-related gene expression sets. We compared 18 human and mouse tissues, and found 9 significantly correlated tissue pairs. Functional analysis also revealed some terms related to aging in human and mouse. And we performed a crosswise comparison of homologous age-related genes with 18 tissues in human and mouse respectively, and found that human Brain_Cortex was significantly correlated with Brain_Hippocampus, which was also found in mouse. In addition, we focused on comparing four brain-related tissues in human and mouse, and found a gene–GFAP–related to aging in both human and mouse. Nature Publishing Group UK 2019-04-17 /pmc/articles/PMC6470208/ /pubmed/30996271 http://dx.doi.org/10.1038/s41598-019-42485-3 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhuang, Jujuan
Zhang, Lijun
Dai, Shuang
Cui, Lingyu
Guo, Cheng
Sloofman, Laura
Yang, Jialiang
Comparison of multi-tissue aging between human and mouse
title Comparison of multi-tissue aging between human and mouse
title_full Comparison of multi-tissue aging between human and mouse
title_fullStr Comparison of multi-tissue aging between human and mouse
title_full_unstemmed Comparison of multi-tissue aging between human and mouse
title_short Comparison of multi-tissue aging between human and mouse
title_sort comparison of multi-tissue aging between human and mouse
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470208/
https://www.ncbi.nlm.nih.gov/pubmed/30996271
http://dx.doi.org/10.1038/s41598-019-42485-3
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