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Projekt Druckansicht

Der Einfluss der Mitochondrien auf das Altern und die Lebensspanne im kurzlebigen Killifisch Nothobranchius furzeri

Antragsteller Professor Dr. Christoph Englert, seit 1/2016
Fachliche Zuordnung Allgemeine Genetik und funktionelle Genomforschung
Förderung Förderung von 2013 bis 2017
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 233592434
 
Erstellungsjahr 2018

Zusammenfassung der Projektergebnisse

The initial goal of this grant was to analyze the role of the mitochondria in aging of the shortlived killifish Nothobranchius furzeri. The underlying hypothesis was that mitochondrial decline contributes to the aging process in this species. Conversely, enhanced mitochondrial biogenesis and function should alleviate some of the aging-associated symptoms and eventually might even result in a prolonged lifespan. However, the data that we have generated in the context of this proposal did not support this notion. This is not so say that the hypothesis is wrong, but it certainly requires more work to assess the role of the mitochondria for aging in N. furzeri. In a second aspect of this proposal on aging in N. furzeri we have used TALENs and CRISPR/Cas9 to generate mutant alleles of genes that are involved in aging. Two genes that we focused on are tert, encoding the functional subunit of telomerase and the tumor suppressor p53. In both cases we could establish loss-of-function alleles that, when crossed to homozygosity, resulted in a shortened lifespan. Although the respective characterizations have not yet been finished, our data so far suggest that in case of tert the shortened lifespan results from tissue atrophy, while p53 mutants suffer from tumorigenesis. We are currently in the process of finishing the phenotypic and molecular characterization of the mutant animals, write the respective manuscripts and employ the mutants for further studies on aging as well as regeneration.

Projektbezogene Publikationen (Auswahl)

 
 

Zusatzinformationen

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