Biased signaling in naturally occurring mutations of G protein-coupled receptors associated with diverse human diseases

Biochim Biophys Acta Mol Basis Dis. 2021 Jan 1;1867(1):165973. doi: 10.1016/j.bbadis.2020.165973. Epub 2020 Sep 17.

Abstract

G protein-coupled receptors (GPCRs) play critical roles in transmitting a variety of extracellular signals into the cells and regulate diverse physiological functions. Naturally occurring mutations that result in dysfunctions of GPCRs have been known as the causes of numerous diseases. Significant progresses have been made in elucidating the pathophysiology of diseases caused by mutations. The multiple intracellular signaling pathways, such as G protein-dependent and β-arrestin-dependent signaling, in conjunction with recent advances on biased agonism, have broadened the view on the molecular mechanism of disease pathogenesis. This review aims to briefly discuss biased agonism of GPCRs (biased ligands and biased receptors), summarize the naturally occurring GPCR mutations that cause biased signaling, and propose the potential pathophysiological relevance of biased mutant GPCRs associated with various endocrine diseases.

Keywords: Biased signaling; G protein-coupled receptor; Naturally occurring mutation; Pathophysiology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Genetic Diseases, Inborn* / genetics
  • Genetic Diseases, Inborn* / metabolism
  • Humans
  • Mutation*
  • Receptors, G-Protein-Coupled* / genetics
  • Receptors, G-Protein-Coupled* / metabolism
  • Signal Transduction*
  • beta-Arrestins / genetics
  • beta-Arrestins / metabolism

Substances

  • Receptors, G-Protein-Coupled
  • beta-Arrestins