Caspase-mediated cleavage of the ubiquitin-protein ligase Nedd4 during apoptosis.
J Biol Chem
; 273(22): 13524-30, 1998 May 29.
Article
in En
| MEDLINE
| ID: mdl-9593687
ABSTRACT
The onset of apoptosis is coupled to the proteolytic activation of a family of cysteine proteases, termed caspases. These proteases cleave their target proteins after an aspartate residue. Following caspase activation during apoptosis, a number of specific proteins have been shown to be cleaved. Here we show that Nedd4, a ubiquitin-protein ligase containing multiple WW domains and a calcium/lipid-binding domain, is also cleaved during apoptosis induced by a variety of stimuli including Fas-ligation, gamma-radiation, tumor necrosis factor-alpha, C-8 ceramide, and etoposide treatment. Extracts from apoptotic cells also generated cleavage patterns similar to that seen in vivo, and this cleavage was inhibited by an inhibitor of caspase-3-like proteases. In vitro, Nedd4 was cleaved by a number of caspases, including caspase-1, -3, -6, and -7. By site-directed mutagenesis, one of the in vitro caspase cleavage sites in mouse Nedd4 was mapped to a DQPD237 downward arrow sequence, which is conserved between mouse, rat, and human proteins. This is the first report demonstrating that an enzyme of the ubiquitin pathway is cleaved by caspases during apoptosis.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Calcium-Binding Proteins
/
Cysteine Endopeptidases
/
Apoptosis
/
Ubiquitin-Protein Ligases
/
Ligases
Limits:
Animals
/
Humans
Language:
En
Journal:
J Biol Chem
Year:
1998
Document type:
Article
Affiliation country:
Australia