Interaction between RGS7 and polycystin

Emily Kim, Thierry Arnould, Lorenz Sellin, Thomas Benzing, Natalia Comella, Olivier Kocher, Leonidas Tsiokas, Vikas P. Sukhatme, Gerd Walz

Research output: Contribution to journalArticlepeer-review

Abstract

Regulators of G protein signaling (RGS) proteins accelerate the intrinsic GTPase activity of certain Gα subunits and thereby modulate a number of G protein-dependent signaling cascades. Currently, little is known about the regulation of RGS proteins themselves. We identified a short-lived RGS protein, RGS7, that is rapidly degraded through the proteasome pathway. The degradation of RGS7 is inhibited by interaction with a C-terminal domain of polycystin, the protein encoded by PKD1, a gene involved in autosomal- dominant polycystic kidney disease. Furthermore, membranous expression of C- terminal polycystin relocalized RGS7. Our results indicate that rapid degradation and interaction with integral membrane proteins are potential means of regulating RGS proteins.

Original languageEnglish
Pages (from-to)6371-6376
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume96
Issue number11
DOIs
Publication statusPublished - 25 May 1999

Keywords

  • Polycystic kidney disease
  • Protein-protein interaction
  • Yeast two-hybrid system

Fingerprint

Dive into the research topics of 'Interaction between RGS7 and polycystin'. Together they form a unique fingerprint.

Cite this