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Molekulare Grundlagen des verzögerten Alterns bei Säugetieren mit stark divergierenden Alternsraten: Afrikanischen Graumullen Fukomys sp. (Rodentia)

Subject Area Animal Physiology and Biochemistry
Evolution, Anthropology
Biogerontology and Geriatric Medicine
Term from 2013 to 2017
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 236365560
 
Final Report Year 2018

Final Report Abstract

In summary, our results show that the large lifespan differences between breeders and non-breeders in Fukomys sp. are not caused by globally altered gene expression but presumably by more subtle changes that specifically affect mainly endocrine tissues and selected pathways. Many of the results underline the importance of target genes and concepts that are already heavily examined in aging research including our previous works, e.g. the mTOR-pathway or proteolytic systems. On the other hand, they also reveal interesting contradictions to the current knowledge, e.g. that strong up-regulation of protein synthesis and IGF1 in breeders are compatible with considerable lifespan extensions. We are optimistic that our results will contribute to new, more system-oriented perspectives on prolonging life- and healthspans. In that sense, the concrete genes, expression patterns and contradictions that were identified in this study with regard to lifespan regulation may become be promising targets for follow-up studies.

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