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  Reprograming of proteasomal degradation by branched chain amino acid metabolism

Ravanelli, S., Li, Q., Annibal, A., Trifunovic, A., Antebi, A., & Hoppe, T. (2022). Reprograming of proteasomal degradation by branched chain amino acid metabolism. Aging Cell, e13725. doi:10.1111/acel.13725.

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https://www.ncbi.nlm.nih.gov/pubmed/36168305 (beliebiger Volltext)
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 Urheber:
Ravanelli, S., Autor
Li, Q., Autor
Annibal, A.1, Autor           
Trifunovic, A., Autor
Antebi, A.1, Autor           
Hoppe, T., Autor
Affiliations:
1Department Antebi - Molecular Genetics of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_1942285              

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Schlagwörter: Caenorhabditis elegans aging branched-chain amino acid branched-chain aminotransferase metabolism proteasome proteostasis ubiquitin
 Zusammenfassung: Branched-chain amino acid (BCAA) metabolism is a central hub for energy production and regulation of numerous physiological processes. Controversially, both increased and decreased levels of BCAAs are associated with longevity. Using genetics and multi-omics analyses in Caenorhabditis elegans, we identified adaptive regulation of the ubiquitin-proteasome system (UPS) in response to defective BCAA catabolic reactions after the initial transamination step. Worms with impaired BCAA metabolism show a slower turnover of a GFP-based proteasome substrate, which is suppressed by loss-of-function of the first BCAA catabolic enzyme, the branched-chain aminotransferase BCAT-1. The exogenous supply of BCAA-derived carboxylic acids, which are known to accumulate in the body fluid of patients with BCAA metabolic disorders, is sufficient to regulate the UPS. The link between BCAA intermediates and UPS function presented here sheds light on the unexplained role of BCAAs in the aging process and opens future possibilities for therapeutic interventions.

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 Datum: 2022-09-272022-09-27
 Publikationsstatus: Erschienen
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 Identifikatoren: Anderer: 36168305
DOI: 10.1111/acel.13725
ISSN: 1474-9726 (Electronic)1474-9718 (Linking)
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Titel: Aging Cell
Genre der Quelle: Zeitschrift
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Seiten: - Band / Heft: - Artikelnummer: - Start- / Endseite: e13725 Identifikator: -