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MITODR

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Determination of evolutionary conserved genes that respond to reduced food intak...

Determination of evolutionary conserved genes that respond to reduced food intake through mitochondria signaling to affect aging The links between diet and lifespan have been revealed 70 years ago but still constitute one of the most mysterious, exciting and extensively studied areas in aging research. In various organisms tested, a restriction of food inta... ver más

31/12/2012

CNRS

50K€

Presupuesto del proyecto: 50K€

Líder del proyecto

CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE... No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Fecha límite participación Sin fecha límite de participación.

Financiación concedida El organismo FP7 notifico la concesión del proyecto el día 2012-12-31 No tenemos la información de la convocatoria

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1 Participantes

CNRS

0.00€ | Lider

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Líder del proyecto

CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE... No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Presupuesto del proyecto 50K€

Fecha límite de participación Sin fecha límite de participación.

Descripción del proyecto The links between diet and lifespan have been revealed 70 years ago but still constitute one of the most mysterious, exciting and extensively studied areas in aging research. In various organisms tested, a restriction of food intake, or DR, can result in lifespan extension up to 50%. In rodents and nonhuman primates, the beneficial effect of DR on longevity is accompanied by reduced incidence of age-related diseases. Thus, as world populations age, understanding how DR impacts animal physiology has far-reaching potentials in term of public health. Recent research has shown that the mitochondrion organelle play an important and evolutionary conserved role in mediating physiologic effects of DR. Our project aims to uncover the molecular changes induced by mitochondria upon DR in C. elegans. We propose to identify genes downstream of mitochondria that affect animal physiology and in particular lifespan upon DR. The nematode C. elegans is an excellent model for this project because of its many powerful genetic and genomic tools. In our first objective, we plan to generate a novel DR model in C. elegans based on its mitochondrial component using chemical and genetics mimics. In our second objective, we propose to identify the gene expression changes specifically induced by mitochondria upon DR. This proposal is likely to reveal new mediators of the cellular adaptations induced by reduced food intake. In addition, our findings will also greatly improve the understanding of mitochondrial signal transduction in controlling whole organism physiology and aging processes. In the future, our research may contribute to therapeutic development of mitochondria-targeted strategies to benefit healthy aging and alleviate age-related diseases.

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