Authors: Sánchez-Blanco A; Kim SK
Abstract: A common property of aging in all animals is that chronologically and genetically identical individuals age at different rates. To unveil mechanisms that influence aging variability, we identified markers of remaining lifespan for Caenorhabditis elegans. In transgenic lines, we expressed fluorescent reporter constructs from promoters of C. elegans genes whose expression change with age. The expression levels of aging markers in individual worms from a young synchronous population correlated with their remaining lifespan. We identified eight aging markers, with the superoxide dismutase gene sod-3 expression being the best single predictor of remaining lifespan. Correlation with remaining lifespan became stronger if expression from two aging markers was monitored simultaneously, accounting for up to 49% of the variation in individual lifespan. Visualizing the physiological age of chronologically-identical individuals allowed us to show that a major source of lifespan variability is different pathogenicity from individual to individual and that the mechanism involves variable activation of the insulin-signaling pathway.
Keywords: Aging/*genetics; Animals; Animals, Genetically Modified/genetics/growth & development/metabolism; Bacillus subtilis/pathogenicity; Caenorhabditis elegans/*genetics/growth & development/microbiology; Caenorhabditis elegans Proteins/genetics/*metabolism; Escherichia coli/pathogenicity; Food; Gene Expression; Genes, Reporter; Green Fluorescent Proteins/metabolism; Longevity; Superoxide Dismutase/genetics/*metabolism
Journal: PLoS genetics Volume: 7 Issue: 4 Pages: e1002047 Date: May 3, 2011 PMID: 21533182 |
Sánchez-Blanco A, Kim SK (2011) Variable pathogenicity determines individual lifespan in Caenorhabditis elegans. PLoS genetics 7: e1002047.
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