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Sterol-regulated degradation of Insig-1 mediated by the membrane-bound ubiquitin ligase gp78.

Insig-1 and Insig-2, closely related endoplasmic reticulum membrane proteins, mediate transcriptional and post-transcriptional mechanisms that assure cholesterol homeostasis through their sterol-induced binding to Scap (SREBP cleavage-activating protein) and 3-hydroxy-3-methylglutaryl coenzyme A reductase. Recent studies show that Insig-1 (but not Insig-2) is ubiquitinated and rapidly degraded when cells are depleted of sterols. Conversely, ubiquitination of Insig-1 is blocked, and the protein is stabilized when intracellular sterols accumulate. Here, we report that the ubiquitin ligase gp78, which binds with much higher affinity to Insig-1 than Insig-2, is required for ubiquitination and degradation of Insig-1 in sterol-depleted cells. Sterols prevent Insig-1 ubiquitination and degradation by displacing gp78 from Insig-1, an event that results from sterol-induced binding of Scap to Insig-1. In addition to providing a mechanism for sterol-regulated degradation of Insig-1, these results help to explain why Scap is subject to endoplasmic reticulum retention upon Insig-1 binding, whereas 3-hydroxy-3-methylglutaryl coenzyme A reductase is ubiquitinated and degraded.

Pubmed ID: 17043353 RIS Download

Mesh terms: Cell Line | Cell Membrane | Endoplasmic Reticulum | Humans | Hydroxymethylglutaryl CoA Reductases | Intracellular Signaling Peptides and Proteins | Membrane Proteins | Models, Biological | Plasmids | Protein Binding | RNA Interference | Receptors, Autocrine Motility Factor | Receptors, Cytokine | Sterols | Ubiquitin | Ubiquitin-Protein Ligases

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Associated grants

  • Agency: NHLBI NIH HHS, Id: HL-20948

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