Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2019 Apr 17;9(1):6220.
doi: 10.1038/s41598-019-42485-3.

Comparison of multi-tissue aging between human and mouse

Affiliations
Comparative Study

Comparison of multi-tissue aging between human and mouse

Jujuan Zhuang et al. Sci Rep. .

Abstract

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.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Workflow of the aging project.
Figure 2
Figure 2
Functional groups in ClueGO Overview. ClueGO analysis of DEGs in Brain_Cerebellum, Brain_Cortex, Brain_Hippocampus and brain from human donors. Overview chart with functional groups including specific terms for DEGs. The percentage of genes per term is shown in each group.
Figure 3
Figure 3
Functionally grouped networks on cerebellum, neocortex, hippocampus and brain for mouse. Functionally grouped network with terms as nodes linked based on their kappa score level (≥ 0.4), where only the label of the most significant term per group is shown. Each node in the figure represents a term, and the node size represents the term enrichment significance. Functionally related groups partially overlap. The connection between the nodes reflects the correlation between the terms, and the color of the node reflects the enrichment classification of the node.

References

    1. Ames BN, Shigenaga MK, Hagen TM. Oxidants, antioxidants, and the degenerative diseases of aging. Proceedings of the National Academy of Sciences of the United States of America. 1993;90:7915–7922. doi: 10.1073/pnas.90.17.7915. - DOI - PMC - PubMed
    1. Beal MF. Aging, energy, and oxidative stress in neurodegenerative diseases. Annals of Neurology. 1995;38:357–366. doi: 10.1002/ana.410380304. - DOI - PubMed
    1. Jousilahti P, Vartiainen E, Tuomilehto J, Puska P. Sex, Age, Cardiovascular Risk Factors, and Coronary Heart Disease. Circulation. 1999;99:1165–1172. doi: 10.1161/01.CIR.99.9.1165. - DOI - PubMed
    1. Salib E. Risk factors for Alzheimer’s disease. Elderly Care. 2000;11:12. - PubMed
    1. Lindsay J, et al. Risk Factors for Alzheimer’s Disease: A Prospective Analysis from the Canadian Study of Health and Aging. American Journal of Epidemiology. 2002;156:445–453. doi: 10.1093/aje/kwf074. - DOI - PubMed

Publication types

Substances