Abstract：
:The ER-associated degradation (ERAD) pathway serves as an important cellular safeguard by directing incorrectly folded and unassembled proteins from the ER to the proteasome. Still, however, little is known about the components mediating ERAD of membrane proteins. Here we show that the evolutionary conserved rhomboid family protein RHBDL4 is a ubiquitin-dependent ER-resident intramembrane protease that is upregulated upon ER stress. RHBDL4 cleaves single-spanning and polytopic membrane proteins with unstable transmembrane helices, leading to their degradation by the canonical ERAD machinery. RHBDL4 specifically binds the AAA+-ATPase p97, suggesting that proteolytic processing and dislocation into the cytosol are functionally linked. The phylogenetic relationship between rhomboids and the ERAD factor derlin suggests that substrates for intramembrane proteolysis and protein dislocation are recruited by a shared mechanism.
journal_name
Mol Celljournal_title
Molecular cellauthors
Fleig L,Bergbold N,Sahasrabudhe P,Geiger B,Kaltak L,Lemberg MKdoi
10.1016/j.molcel.2012.06.008subject
Has Abstractpub_date
2012-08-24 00:00:00pages
558-69issue
4eissn
1097-2765issn
1097-4164pii
S1097-2765(12)00503-5journal_volume
47pub_type
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