ANTAGING

The role of somatic mutation in the lifespan difference of queen and worker ants

 Coordinatore UNIVERSITE DE LAUSANNE 

 Organization address city: LAUSANNE
postcode: 1015

contact info
Titolo: Prof.
Nome: Laurent
Cognome: Keller
Email: send email
Telefono: +41 21 6924173
Fax: +41 21 6924165

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 184˙709 €
 EC contributo 184˙709 €
 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) 2012-04-01   -   2014-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE DE LAUSANNE

 Organization address city: LAUSANNE
postcode: 1015

contact info
Titolo: Prof.
Nome: Laurent
Cognome: Keller
Email: send email
Telefono: +41 21 6924173
Fax: +41 21 6924165

CH (LAUSANNE) coordinator 184˙709.40

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

age    species    genes    exist    ros    damage    social    pcr    theory    repair    aging    free    lifespan    lived    workers    predicted    mutations    life    agents    insect    niger    live    radical    expression    removal    years    queens    longer    dna    senescence   

 Obiettivo del progetto (Objective)

'The social insects provide a unique system for the study of aging and senescence. The striking differences in longevity that exist between queens and workers can be used to examine how different life histories can lead to very different aging patterns despite shared genetic heritage. In the ant Lasius niger, for example, workers live up to two years while queens have been known to live as long as 29 years. For this reason, insect societies have been used to test models such as the free radical theory of aging. This model predicts that longer lifespan can be achieved by investing more resources into the removal from the organism of damaging oxidising agents such as Reactive Oxygen Species (ROS). These agents are predicted to damage not only lipids and proteins, but also DNA by generating mutations. The accumulation of such mutations in the soma (non germ-line tissues) over time are assumed to play a part in the degeneration associated with senescence. Intrigingly, studies on social insect systems have consistently found results opposite to expectations: shorter-lived workers show greater expression of ROS removal genes than longer-lived queens. It is necessary now to take a step back and ask whether the different levels of damage of the type predicted by the free radical theory, such as DNA mutations, do indeed exist. Furthermore, enquiries are needed into whether the counter-intuitive pattern shown by ROS-removal genes are consistent across other maintenance processes such as DNA repair. Using quantitative PCR and single-molecule PCR, and using L. niger as a study species, I aim to find out: a. Whether queens and workers show an increase in somatic DNA mutations with age. b. Whether this increase occurs more rapidly in workers than queens. c. Whether queens invest more than workers in expression of DNA repair genes. This study will further our understanding of the causes of senescence and of the evolution of life history strategies that can prolong lifespan.'

Introduzione (Teaser)

Unlocking the secrets of ageing promises to be the key to developing therapies for many chronic and age-related diseases. The startling difference between lifespan of worker ants (2 years) and queens (up to 29 years) provided an EU-funded project with insight on the molecular basis behind senescence.

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