Proteomics

Dataset Information

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Analysis of C. elegans DAF-16 phosphorylation in different genetic backgrounds.


ABSTRACT: C. elegans DAF-16/FOXO phosphorylation in different genetic backgrounds was analyzed by mass spectrometry of affinity purified HA-tagged DAF-16. Genetic backgrounds studied include par-1 hypomorphic mutants, PAR-1 knockdown using an auxin-inducible degron (AID), daf-2(e1370) and akt-1(ok525) mutants. PAR-1 is the C. elegans ortholog of MARK kinases; DAF-2 is the sole C. elegans insulin/IGF receptor, and AKT-1 is one of two AKT kinases in the nematode.

INSTRUMENT(S):

ORGANISM(S): Caenorhabditis Elegans

SUBMITTER: Markus Hartl  

LAB HEAD: Mario de Bono

PROVIDER: PXD053590 | Pride | 2025-12-29

REPOSITORIES: Pride

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Publications

Proximity labeling of DAF-16 FOXO highlights aging regulatory proteins.

Artan Murat M   Schoen Hanna H   de Bono Mario M  

Nature communications 20251211 1


Insulin/insulin-like growth factor signaling inhibits FOXO transcription factors to control development, homeostasis, and aging. Here, we use proximity labeling to identify proteins interacting with the C. elegans FOXO DAF-16. We show that in well-fed, unstressed animals harboring active insulin signaling, DAF-16 forms a complex with the PAR-1/MARK serine/threonine kinase, a key regulator of cell polarity. PAR-1 inhibits DAF-16 accumulation and promotes DAF-16 phosphorylation at S249, at a conse  ...[more]

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