Abstract

Understanding the biological mechanisms behind aging, lifespan and healthspan is becoming increasingly important as the proportion of the world's population over the age of 65 grows, along with the cost and complexity of their care. BigData oriented approaches and analysis methods enable current and future bio-gerontologists to synthesize, distill and interpret vast, heterogeneous data from functional genomics studies of aging. GeneWeaver is an analysis system for integration of data that allows investigators to store, search, and analyze immense amounts of data including user-submitted experimental data, data from primary publications, and data in other databases. Aging related genome-wide gene sets from primary publications were curated into this system in concert with data from other model-organism and aging-specific databases, and applied to several questions in genrontology using. For example, we identified Cd63 as a frequently represented gene among aging-related genome-wide results. To evaluate the role of Cd63 in aging, we performed RNAi knockdown of the C. elegans ortholog, tsp-7, demonstrating that this manipulation is capable of extending lifespan. The tools in GeneWeaver enable aging researchers to make new discoveries into the associations between the genes, normal biological processes, and diseases that affect aging, healthspan, and lifespan.

Highlights

  • The population of individuals aged 65 and over is projected to be approximately 83.7 million in 2050, almost double its estimated number of 43.1 million in 2012 [1]

  • GeneWeaver was queried to identify gene sets related to the biological process of cellular senescence and phenotype of cognitive decline

  • Ingenuity Pathway Analysis (IPA) revealed that the intersection is significantly enriched with UVC-MAP kinase pathway members

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Summary

Introduction

The population of individuals aged 65 and over is projected to be approximately 83.7 million in 2050, almost double its estimated number of 43.1 million in 2012 [1]. Aging affects the entire organism, with age-associated decline occurring across organ systems and within distinct tissues and cell-types. Heterogeneous data integration identifies new aging genes and pathways

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