Coordinatore | UNIVERSITY OF GLASGOW
Organization address
address: University Avenue contact info |
Nazionalità Coordinatore | United Kingdom [UK] |
Totale costo | 200˙371 € |
EC contributo | 200˙371 € |
Programma | FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
Code Call | FP7-PEOPLE-2011-IEF |
Funding Scheme | MC-IEF |
Anno di inizio | 2012 |
Periodo (anno-mese-giorno) | 2012-06-01 - 2014-05-31 |
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UNIVERSITY OF GLASGOW
Organization address
address: University Avenue contact info |
UK (GLASGOW) | coordinator | 200˙371.80 |
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'EVOTELOX seeks to examine the extent to which environmentally driven variations in early life nutrition influences oxidative status and telomere loss in vivo, and thereby the costs and benefits of different life history trajectories. Despite the promising role of telomere biology in understanding the biology of life spam, currently little is known about factor that affect telomere dynamics in natural systems and whether telomere dynamics during early life may constraint life history traits. The main objectives of this project are to (1) examine the effect of dietary antioxidants on oxidative status and telomere loss of Zebra finches during their early development and (2) investigate the effect of early life nutrition and telomere dynamics on sexual maturation and reproduction during adulthood. We will use a multidisciplinary approach, combining ‘state of the art’ techniques in evolutionary biology, gerontology and ecophysiology to quantify telomere length and the level of oxidative stress in addition to manipulative experiments. The ultimate aim of this study is establishing sustainable collaboration between the host institute and fellow for the future researches in the fellow’s country of origin. We will continue cooperation to obtain advanced expertise on model systems and physiology of life history trade-offs.'
A recent research project has investigated the effects of poor nutrition on lifespan and reproductive success in finches.
It is well known that poor nutrition leads to compromised development but the causal mechanisms, and the extent and duration of the effects, are unclear. In particular, it would be valuable to understand the effect of diet on the length of telomeres. The telomeres are specialised pieces of DNA at the ends of chromosomes; these wear away with time, and the rate at which this happens influences the rate of ageing.
The EU-funded EVOTELOX project aimed to study this in zebra finches (Taeniopygia guttata). Specifically, researchers wanted to know how diet during development affects antioxidant status and telomere dynamics, and how these influence individual investment in reproduction.
Initially, EVOTELOX measured the physiological effects of different dietary micronutrient levels early in life on overall development, sexual maturity, oxidative status and telomere length. In a follow-up experiment, the birds were bred with a known partner to measure the effect of early life diet on reproduction and offspring growth.
The researchers found that antioxidant defences and telomere length were both severely affected by dietary micronutrient levels; birds reared on a low micronutrient diet showed lower antioxidant defences and showed an accelerated loss of telomeres, particularly during sexual maturation. Moreover, the family of origin had a strong effect on both telomere length and loss rate, suggesting a genetic influence on both traits.
During sexual maturation, birds fed a low micronutrient diet showed an accelerated development of adult bill colour. Interestingly, the rate of telomere loss and bill colour development was positively correlated during this period, suggesting that birds experiencing an increased telomere loss rate had faster sexual maturation.
Finally, EVOTELOX also showed that females reared on a low micronutrient diet during their development tended to invest more in reproduction at adulthood (e.g. more breeding attempts) than any other experimental group. However, when reproducing, these females had smaller clutches, lower hatching success and their offspring showed lower growth rates. These findings represent an important contribution to our understanding of nutritional modulation of (human) ageing and life history plasticity, and intergenerational effects.