News Release

Short-lived killifish reveals link between gene expression and longevity

Peer-Reviewed Publication

Cell Press

Gene Expression and Lifespan in the Killifish

image: This visual abstract depicts the longitudinal transcriptome analyses that was performed in a short-lived fish by taking two fin clips during early adult life to correlate gene expression with lifespan. Gene-coexpression network analysis identified complex I of the mitochondrial respiratory chain as a hub for negative correlation with lifespan, and its pharmacological inhibition prolonged lifespan and rejuvenated the transcriptome. view more 

Credit: Baumgart and Priebe et al./Cell Systems 2016

It's well known that genetic differences among individuals influence lifespan, but a new study appearing February 24 in Cell Systems suggests that differences in patterns of gene expression in youth may also predict longevity. Researchers of the shortest-lived vertebrate--the African turquoise killifish--found that when genes involved in a cell's energy production are less active at a young age, the animals tend to live longer.

Alessandro Cellerino of the Scuola Normale Superiore in Pisa, Italy, and the Leibniz Institute on Aging in Jena, Germany, and his colleagues analyzed the expression of genes in small biopsies from the fins of killifish at different times during the animals' lives, and they divided the fish into groups based on their longevity. Even under optimal conditions, the fish do not live beyond 4 to 12 months.

The team discovered that genes that are responsible for cellular respiration--the process by which mitochondria within cells use oxygen to burn sugar and produce energy--were less active at a young age in the fish that were long-lived.

When the researchers exposed the fish to a very low dose of a natural poison called rotenone, which inhibits the proteins (that collectively form mitochondrial complex I) responsible for the first step of cellular respiration, the fish lived longer.

While more information is needed to determine if the findings apply to humans, Cellerino notes that the function of mitochondria decreases with age in both humans and killifish alike. "Up to the present, it was thought that improving mitochondrial function would improve health in aged people; however, our results indicate a more complex scenario where the partial inhibition of mitochondrial function paradoxically has beneficial effects," he says.

This may occur because such inhibition produces a small amount of free radicals that do not harm the cells but can stimulate a positive, adaptive response. "This mechanism of adaptation after stress is called hormesis, and it was recently demonstrated that the positive effects of physical exercise in humans are due to hormesis and are destroyed by treatment with antioxidants," Cellerino explains.

This latest research suggests that the effects of aging on mitochondria may involve a compensatory response rather than one that causes problems. "This obviously has implications on the development of strategies to improve health in older people and prevent aging-associated diseases," Cellerino says.

Interestingly, there are FDA-approved drugs that inhibit mitochondrial complex I. Metformin, one such drug that is prescribed to treat type 2 diabetes, has been shown to extend the lifespan of mice. "Based on our data, we strongly suspect that the effect of metformin was due to inhibition of complex I and not to its anti-diabetic action," he says.

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This work was partially supported by the German Ministry for Education and Research and by an intramural grant of Scuola Normale Superiore.

Cell Systems, Baumgart and Priebe et al.: "Longitudinal RNA-Seq Analysis of Vertebrate Aging Identifies Mitochondrial Complex I as a Small-Molecule-Sensitive Modifier of Lifespan" http://dx.doi.org/10.1016/j.cels.2016.01.014

Cell Systems (@CellSystemsCP), published by Cell Press, is a monthly journal featuring papers that provide, support, or apply systems-level understanding in the life sciences and related disciplines. Research describes novel discoveries, milestone achievements, applied research, translational findings, broadly useful tools or resources, or insights into the use of technology. For more information, please visit http://www.cell.com/cell-systems. To receive Cell Press media alerts, contact press@cell.com.


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