Summary
Despite being one of the most familiar biological process affecting our lives, little is known about the molecular mechanics of ageing. A better understanding of ageing and related diseases is today crucial to face its deleterious effects on our growing older population. Among mammals bigger species typically live longer than smaller ones. When corrected for body size, almost all mammals have the same longevity quotients, exception made for the chiroptera. Bats are capable of living up to 10 times longer than expected despite their characteristic high metabolic rates. During my doctorate, I discovered the presence of a distinctive behaviour in bats' autophagic pathway, suggesting that these animals may rely on an improved system for intracellular proteostasis accounting for the flight-associated high metabolic stress. The same evolutive adaptation could ultimately have played a role in allowing bats to achieve exceptional longevity. Here I propose to carry out an in-depth analysis of the proteostatic system, and in particular of the autophagic pathway, in bats. Samples from wild populations of bats will be used to derive primary cell lines allowing to characterise bats’ intracellular phenotype and proteostatic activity. Thanks to the expert personnel and cutting-edge facilities of the hosting institute, I will exploit imaging and proteomics tools to isolate bat-specific molecular features of adaptation in proteostasis and unveil their role in determining their unique ageing pattern. A complementary phylogenomic analysis will be performed to detect traces of adaptive selection in proteostasis-associated genes in bats and other mammals. For the first time, the complexity of interactions behind proteostasis and ageing will be examined from a privileged, integrative perspective. This innovative project holds huge potential as it could lead to a greater understanding of the role of protein homeostasis in mammalian ageing contributing to dampen its effects on our society.
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More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/894917 |
| Start date: | 01-09-2021 |
| End date: | 31-08-2023 |
| Total budget - Public funding: | 183 473,28 Euro - 183 473,00 Euro |
Cordis data
Original description
Despite being one of the most familiar biological process affecting our lives, little is known about the molecular mechanics of ageing. A better understanding of ageing and related diseases is today crucial to face its deleterious effects on our growing older population. Among mammals bigger species typically live longer than smaller ones. When corrected for body size, almost all mammals have the same longevity quotients, exception made for the chiroptera. Bats are capable of living up to 10 times longer than expected despite their characteristic high metabolic rates. During my doctorate, I discovered the presence of a distinctive behaviour in bats' autophagic pathway, suggesting that these animals may rely on an improved system for intracellular proteostasis accounting for the flight-associated high metabolic stress. The same evolutive adaptation could ultimately have played a role in allowing bats to achieve exceptional longevity. Here I propose to carry out an in-depth analysis of the proteostatic system, and in particular of the autophagic pathway, in bats. Samples from wild populations of bats will be used to derive primary cell lines allowing to characterise bats’ intracellular phenotype and proteostatic activity. Thanks to the expert personnel and cutting-edge facilities of the hosting institute, I will exploit imaging and proteomics tools to isolate bat-specific molecular features of adaptation in proteostasis and unveil their role in determining their unique ageing pattern. A complementary phylogenomic analysis will be performed to detect traces of adaptive selection in proteostasis-associated genes in bats and other mammals. For the first time, the complexity of interactions behind proteostasis and ageing will be examined from a privileged, integrative perspective. This innovative project holds huge potential as it could lead to a greater understanding of the role of protein homeostasis in mammalian ageing contributing to dampen its effects on our society.Status
CLOSEDCall topic
MSCA-IF-2019Update Date
28-04-2024
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