Background The regulation of Notch signaling heavily relies on ubiquitination events. Drosophila Su(dx), a member of the HECT family of ubiquitin-ligases, has been described as a negative regulator of Notch signaling, acting on the post-endocytic sorting of Notch. The mammalian ortholog of Su(dx), Itch/AIP4, has been shown to have multiple substrates, including Notch, but the precise events regulated by Itch/AIP4 in the Notch pathway have not been identified yet. Methodology/Principal Findings Using Itch-/- fibroblasts expressing the Notch1 receptor, we show that Itch is not necessary for Notch activation, but rather for controlling the degradation of Notch in the absence of ligand. Itch is indeed required after the early steps of Notch endocytosis to target it to the lysosomes where it is degraded. Furthermore Itch/AIP4 catalyzes Notch polyubiquitination through unusual K29-linked chains. We also demonstrate that although Notch is associated with Itch/AIP4 in cells, their interaction is not detectable in vitro and thus requires either a post-translational modification, or a bridging factor that remains to be identified. Conclusions/Significance Taken together our results identify a specific step of Notch regulation in the absence of any activation and underline differences between mammalian and Drosophila Notch pathways.
AIP4/Itch Regulates Notch Receptor Degradation in the Absence of Ligand
P. Chastagner,A. Israël,C. Brou
Published 2008 in PLoS ONE
ABSTRACT
PUBLICATION RECORD
- Publication year
2008
- Venue
PLoS ONE
- Publication date
2008-07-16
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
CITATION MAP
EXTRACTION MAP
CLAIMS
CONCEPTS
- itch/aip4
A mammalian HECT-family ubiquitin ligase, also known as AIP4 or Itch, examined here as a regulator of Notch receptor trafficking.
Aliases: AIP4, Itch, AIP4/Itch
박진우 (dztg5apj7m) extractionB (s683577b42) reviewq (76h6bfydm6) reviewAnonymous (n259mg7uxy) reviewAK (4715169a40) review - itch-/- fibroblasts
Fibroblast cells genetically lacking Itch that were used to test Notch receptor regulation in a mammalian cell context.
Aliases: Itch knockout fibroblasts, Itch-null fibroblasts
박진우 (dztg5apj7m) extractionB (s683577b42) reviewq (76h6bfydm6) reviewAnonymous (n259mg7uxy) reviewAK (4715169a40) review - k29-linked polyubiquitin chains
A ubiquitin chain architecture in which ubiquitin molecules are linked through lysine 29 of ubiquitin.
Aliases: K29 chains, Lys29-linked chains
박진우 (dztg5apj7m) extractionB (s683577b42) reviewq (76h6bfydm6) reviewAnonymous (n259mg7uxy) reviewAK (4715169a40) review - ligand absence
The condition in which Notch signaling is assessed without exposure to a receptor-activating ligand.
Aliases: absence of ligand, no ligand
박진우 (dztg5apj7m) extractionB (s683577b42) reviewq (76h6bfydm6) reviewAnonymous (n259mg7uxy) reviewAK (4715169a40) review - lysosomes
Acidic degradative organelles that receive cargo for proteolytic breakdown in the endocytic pathway.
박진우 (dztg5apj7m) extractionB (s683577b42) reviewq (76h6bfydm6) reviewAnonymous (n259mg7uxy) reviewAK (4715169a40) review - notch1 receptor
The Notch receptor isoform analyzed in the fibroblast experiments for endocytosis, ubiquitination, and degradation.
Aliases: Notch1
박진우 (dztg5apj7m) extractionB (s683577b42) reviewq (76h6bfydm6) reviewAnonymous (n259mg7uxy) reviewAK (4715169a40) review - notch receptor degradation
The breakdown of internalized Notch receptor as part of its post-endocytic fate.
Aliases: Notch degradation
박진우 (dztg5apj7m) extractionB (s683577b42) reviewq (76h6bfydm6) reviewAnonymous (n259mg7uxy) reviewAK (4715169a40) review - post-endocytic sorting
The trafficking step that directs internalized Notch toward specific intracellular destinations after endocytosis.
Aliases: post-endocytic trafficking
박진우 (dztg5apj7m) extractionB (s683577b42) reviewq (76h6bfydm6) reviewAnonymous (n259mg7uxy) reviewAK (4715169a40) review
REFERENCES
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