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Projekt Druckansicht

Woodhouse-Sakati-Syndrom: Untersuchung von Alterungsprozessen anhand einer neuen Progerie-Erkrankung

Antragstellerin Dr. Daniela Bakula
Fachliche Zuordnung Zellbiologie
Förderung Förderung von 2017 bis 2019
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 393041795
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

In total, my project revealed that the monogenic disorder Woodhouse-Sakati syndrome can be classified as a new premature aging disease. The disease is caused by mutations in the gene DCAF17, encoding a protein that has been suggested to function in the CUL4A-DDB1 E3 ubiquitin ligase complex. However, there is no mechanistic understanding of the DCAF17-containing protein complex and thus, the underlying pathogenesis of Woodhouse-Sakati syndrome remains a mystery. In this study, we describe the first Scandinavian patients suffering from Woodhouse-Sakati syndrome. The patients display several features of aging, which were further supported by the observation of increased cellular senescence in isolated peripheral blood mononuclear cells of the patients. Further, my data unravel novel interaction characteristics of the DDB1-DDA1-DCAF17 protein complex and how those affect the stability of the protein complex. DCAF17, itself, is recruited to the DNA damage site, and in line with this, loss of DCAF17 leads to decreased genome stability and altered DNA metabolism. In summary, our findings corroborate the role of DNA maintenance as critical for healthy aging. Future research on substrate recognition of the DCAF17-containing DDB1 E3 ubiquitin ligase complex will be necessary to fully understand the pathomechanism of the disease.

Projektbezogene Publikationen (Auswahl)

 
 

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