Orphan receptor GPR158 serves as a metabotropic glycine receptor: mGlyR

Author:

Laboute Thibaut1ORCID,Zucca Stefano1ORCID,Holcomb Matthew2ORCID,Patil Dipak N.1ORCID,Garza Chris2ORCID,Wheatley Brittany A.3ORCID,Roy Raktim N.3ORCID,Forli Stefano2ORCID,Martemyanov Kirill A.1ORCID

Affiliation:

1. Department of Neuroscience, UF Scripps Biomedical Research, Jupiter, FL 33458, USA.

2. Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037 USA.

3. Department of Integrative Structural and Computational Biology, UF Scripps Biomedical Research, Jupiter, FL 33458, USA.

Abstract

Glycine is a major neurotransmitter involved in several fundamental neuronal processes. The identity of the metabotropic receptor mediating slow neuromodulatory effects of glycine is unknown. We identified an orphan G protein–coupled receptor, GPR158, as a metabotropic glycine receptor (mGlyR). Glycine and a related modulator, taurine, directly bind to a Cache domain of GPR158, and this event inhibits the activity of the intracellular signaling complex regulator of G protein signaling 7–G protein β5 (RGS7-Gβ5), which is associated with the receptor. Glycine signals through mGlyR to inhibit production of the second messenger adenosine 3′,5′-monophosphate. We further show that glycine, but not taurine, acts through mGlyR to regulate neuronal excitability in cortical neurons. These results identify a major neuromodulatory system involved in mediating metabotropic effects of glycine, with implications for understanding cognition and affective states.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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