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JUMPn: A Streamlined Application for Protein Co-Expression Clustering and Network Analysis in Proteomics
Published on: October 19, 2021
Analysis of aging-related protein interactome and cross-network module comparisons across tissues provide new
1Virology Unit and Bioinformatics Centre, Institute of Microbial Technology, Council of Scientific & Industrial Research, Chandigarh, 160036, India.
Abstract:
Delaying the human aging process and thus eliminating the risk factors for age-related diseases is one of the prime objectives. While various aging-associated genes and proteins have been characterized, which provide a significant understanding of the human aging process, a significant success in regulating aging is not achieved yet. Understanding how aging proteins interact with each other and also with other proteins could provide important insights into the underlying mechanisms governing the aging process. Therefore, in this work, information of gene expression was included to the static aging-related protein interactome to understand the network-based relationships among aging-related essential (AE) proteins, aging-related non-essential (ANE) proteins, and housekeeping-proteins that could regulate or influence aging. Comprehensive analyses provided various systems-level insights into the regulatory characteristics of aging; for example, (i) network-based correlation analysis predicted functional relationships among AE proteins and ANE proteins; (ii) network variability analysis predicted aging to affect different tissues in strikingly different ways by differentially regulating various regulatory interactions; (iii) cross-network comparisons identified two aging-related modules to be significantly conserved across most of the tissues. Overall, the findings obtained during this study could be helpful for researchers to delay, prevent, or even reverse various aspects of the aging.
Insights
This study integrates gene expression with protein interactions to map aging networks. Findings reveal how aging affects tissues differently and identify conserved aging modules, offering insights to potentially delay or reverse aging.
Area of Science:
- Biogerontology
- Systems Biology
- Computational Biology
Background:
- Delaying human aging and preventing age-related diseases are key research goals.
- Understanding protein interactions is crucial for elucidating aging mechanisms.
- Current knowledge of aging-associated genes and proteins has not yet led to significant aging regulation success.
Purpose of the Study:
- To integrate gene expression data with the aging-related protein interactome.
- To analyze network-based relationships among aging-related essential (AE) proteins, aging-related non-essential (ANE) proteins, and housekeeping proteins.
- To gain systems-level insights into the regulatory characteristics of aging.
Main Methods:
- Incorporation of gene expression information into a static aging-related protein interactome.
- Network-based correlation analysis to predict functional relationships between AE and ANE proteins.
- Network variability analysis to assess tissue-specific regulation of aging.
- Cross-network comparisons to identify conserved aging-related modules.
Main Results:
- Predicted functional relationships among aging-related proteins.
- Demonstrated that aging impacts different tissues uniquely through differential regulation of interactions.
- Identified two aging-related modules conserved across most tissues.
Conclusions:
- The study provides systems-level insights into aging regulation.
- Findings can guide researchers in developing strategies to delay, prevent, or reverse aging.
- Understanding protein interaction networks is vital for aging research.
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