Scientists at the University of Birmingham funded by the Biotechnology and Biological Sciences Research Council (BBSRC) have discovered that a gene called DAF-16 is strongly involved in determining the rate of ageing and average lifespan of the laboratory worm Caenorhabditis elegans (C. elegans) and its close evolutionary cousins.
DAF-16 is found in many other animals, including humans. It is possible that this knowledge could open up new avenues for altering ageing, immunity and resistance to stresses in humans. The research was published (01 April) in PLoS ONE.
Dr Robin May from the University’s College of Life and Environmental Sciences, who led the research said: “Ageing is a process that all organisms experience, but at very different rates. We know that, even between closely related species, average lifespans can vary enormously.
“We wanted to find out how normal ageing is being governed by genes and what effect these genes have on other traits, such as immunity. To do that, we looked at a gene that we already knew to be involved in the ageing process, called DAF-16, to see how it may determine the different rates of ageing in different species.”
Dr May and colleagues compared longevity, stress resistance and immunity in four related species: Caenorhabditis elegans, Caenorhabditis briggsae, Caenorhabditis remanei and Caenorhabditis brenneri. They also looked for differences in the activity of DAF-16 in each of the four species and found that they were all quite distinct in this respect. And, importantly, the differences in DAF-16 corresponded exactly to differences in longevity, stress resistance and imunity in the four species – in general more DAF-16 activity means longer life, increased stress resistance and better immunity against some but not all diseases.
Dr May continued: “DAF-16 is part of a group of genes that drive the biological processes involved in ageing, immunity and responses to physical or environmental stresses. The fact that subtle differences in DAF-16 between species seem to have such an impact on ageing and health is very interesting and may explain how differences in lifespan and related traits have arisen during evolution.”
The research in Birmingham is now moving on to look at the way in which DAF-16 coordinates a complex network of genes in order to balance the differing needs of an individual’s immune system over time.
Professor Douglas Kell said: “Research using model organisms that uncovers the biology underpinning ageing gives us the opportunity to understand some of the mechanisms that determine how humans age in a healthy, or at least normal, way. It is very important to develop a good understanding of healthy ageing if we are to appreciate what happens to an older person’s physiology when they become unwell or experience difficulties with everyday tasks such as recalling memories or moving around. Improving the healthspan to mirror increases in the lifespan is an important subject of BBSRC research.”
DAF-16 is part of a system within the nematode worms that is important in the ‘dauer’ stage of development and also affects life span and reproduction. The protein that is encoded by this gene is of a class called ‘forkhead transcription factors’, which act to control the expression of other genes. It is active in most cells and is very similar to human genes called FOXO1, FOXO3, FOXO4 and FOXO6.
To investigate lifespan, the researchers compared the longevity of four species of nematode worm (Caenorhabditis elegans, Caenorhabditis briggsae, Caenorhabditis remanei and Caenorhabditis brenneri) and also the expression of DAF-16. They found, for example, that Caenorhabditis remanei lives longer than Caenorhabditis elegans and DAF-16 expression is also 12 fold higher.
Research into the stress resistance and immunity of the four species involved exposing them to high temperature, heavy metals and a range of bacterial and fungal diseases. Those species with higher DAF-16 expression are generally more resistant to these stresses than those with lower DAF-16 expression, although in the case of salmonella infection, there was little difference between the four.
Contacts and sources:
Dr Robin May, Tel 0121 4145418 or 0777 2971319, email: firstname.lastname@example.org