Arrestin domain‐containing protein 3 recruits the NEDD4 E3 ligase to mediate ubiquitination of the β2‐adrenergic receptor

JF Nabhan, H Pan, Q Lu - EMBO reports, 2010 - embopress.org
JF Nabhan, H Pan, Q Lu
EMBO reports, 2010embopress.org
Prolonged stimulation of the β2‐adrenergic receptor (β2AR) leads to receptor ubiquitination
and downregulation. Using a genome‐wide RNA interference screen, we identified arrestin
domain‐containing 3 (ARRDC3) as a gene required for β2AR regulation. The ARRDC3
protein interacts with ubiquitin ligase neural precursor development downregulated protein
4 (NEDD4) through two conserved PPXY motifs and recruits NEDD4 to the activated
receptor. The ARRDC3 protein also interacts and co‐localizes with activated β2AR …
Prolonged stimulation of the β2‐adrenergic receptor (β2AR) leads to receptor ubiquitination and downregulation. Using a genome‐wide RNA interference screen, we identified arrestin domain‐containing 3 (ARRDC3) as a gene required for β2AR regulation. The ARRDC3 protein interacts with ubiquitin ligase neural precursor development downregulated protein 4 (NEDD4) through two conserved PPXY motifs and recruits NEDD4 to the activated receptor. The ARRDC3 protein also interacts and co‐localizes with activated β2AR. Knockdown of ARRDC3 expression abolishes the association between NEDD4 and β2AR. Furthermore, functional inactivation of ARRDC3, either through small interfering RNA (siRNA)‐mediated knockdown or overexpression of a mutant that does not interact with NEDD4, blocks receptor ubiquitination and degradation. Our results establish ARRDC3 as an essential adaptor for β2AR ubiquitination.
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