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Identification of homologous GluN subunits variants accelerates GRIN variants stratification
The clinical spectrum of GRIN-related neurodevelopmental disorders (GRD) results from gene- and variant-dependent primary alterations of the NMDA receptor, disturbing glutamatergic neurotransmission. Despite GRIN gene variants’ functional annotations being dually critical for stratification and prec...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816381/ https://www.ncbi.nlm.nih.gov/pubmed/36619673 http://dx.doi.org/10.3389/fncel.2022.998719 |
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author | Santos-Gómez, Ana García-Recio, Adrián Miguez-Cabello, Federico Soto, David Altafaj, Xavier Olivella, Mireia |
author_facet | Santos-Gómez, Ana García-Recio, Adrián Miguez-Cabello, Federico Soto, David Altafaj, Xavier Olivella, Mireia |
author_sort | Santos-Gómez, Ana |
collection | PubMed |
description | The clinical spectrum of GRIN-related neurodevelopmental disorders (GRD) results from gene- and variant-dependent primary alterations of the NMDA receptor, disturbing glutamatergic neurotransmission. Despite GRIN gene variants’ functional annotations being dually critical for stratification and precision medicine design, genetically diagnosed pathogenic GRIN variants currently outnumber their relative functional annotations. Based on high-resolution crystal 3D models and topological domains conservation between GluN1, GluN2A, and GluN2B subunits of the NMDAR, we have generated GluN1-GluN2A-GluN2B subunits structural superimposition model to find equivalent positions between GluN subunits. We have developed a GRIN structural algorithm that predicts functional changes in the equivalent structural positions in other GluN subunits. GRIN structural algorithm was computationally evaluated to the full GRIN missense variants repertoire, consisting of 4,525 variants. The analysis of this structure-based model revealed an absolute predictive power for GluN1, GluN2A, and GluN2B subunits, both in terms of pathogenicity-association (benign vs. pathogenic variants) and functional impact (loss-of-function, benign, gain-of-function). Further, we validated this computational algorithm experimentally, using an in silico library of GluN2B-equivalent GluN2A artificial variants, designed from pathogenic GluN2B variants. Thus, the implementation of the GRIN structural algorithm allows to computationally predict the pathogenicity and functional annotations of GRIN variants, resulting in the duplication of pathogenic GRIN variants assignment, reduction by 30% of GRIN variants with uncertain significance, and increase by 70% of functionally annotated GRIN variants. Finally, GRIN structural algorithm has been implemented into GRIN variants Database (http://lmc.uab.es/grindb), providing a computational tool that accelerates GRIN missense variants stratification, contributing to clinical therapeutic decisions for this neurodevelopmental disorder. |
format | Online Article Text |
id | pubmed-9816381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98163812023-01-07 Identification of homologous GluN subunits variants accelerates GRIN variants stratification Santos-Gómez, Ana García-Recio, Adrián Miguez-Cabello, Federico Soto, David Altafaj, Xavier Olivella, Mireia Front Cell Neurosci Cellular Neuroscience The clinical spectrum of GRIN-related neurodevelopmental disorders (GRD) results from gene- and variant-dependent primary alterations of the NMDA receptor, disturbing glutamatergic neurotransmission. Despite GRIN gene variants’ functional annotations being dually critical for stratification and precision medicine design, genetically diagnosed pathogenic GRIN variants currently outnumber their relative functional annotations. Based on high-resolution crystal 3D models and topological domains conservation between GluN1, GluN2A, and GluN2B subunits of the NMDAR, we have generated GluN1-GluN2A-GluN2B subunits structural superimposition model to find equivalent positions between GluN subunits. We have developed a GRIN structural algorithm that predicts functional changes in the equivalent structural positions in other GluN subunits. GRIN structural algorithm was computationally evaluated to the full GRIN missense variants repertoire, consisting of 4,525 variants. The analysis of this structure-based model revealed an absolute predictive power for GluN1, GluN2A, and GluN2B subunits, both in terms of pathogenicity-association (benign vs. pathogenic variants) and functional impact (loss-of-function, benign, gain-of-function). Further, we validated this computational algorithm experimentally, using an in silico library of GluN2B-equivalent GluN2A artificial variants, designed from pathogenic GluN2B variants. Thus, the implementation of the GRIN structural algorithm allows to computationally predict the pathogenicity and functional annotations of GRIN variants, resulting in the duplication of pathogenic GRIN variants assignment, reduction by 30% of GRIN variants with uncertain significance, and increase by 70% of functionally annotated GRIN variants. Finally, GRIN structural algorithm has been implemented into GRIN variants Database (http://lmc.uab.es/grindb), providing a computational tool that accelerates GRIN missense variants stratification, contributing to clinical therapeutic decisions for this neurodevelopmental disorder. Frontiers Media S.A. 2022-12-23 /pmc/articles/PMC9816381/ /pubmed/36619673 http://dx.doi.org/10.3389/fncel.2022.998719 Text en Copyright © 2022 Santos-Gómez, García-Recio, Miguez-Cabello, Soto, Altafaj and Olivella. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular Neuroscience Santos-Gómez, Ana García-Recio, Adrián Miguez-Cabello, Federico Soto, David Altafaj, Xavier Olivella, Mireia Identification of homologous GluN subunits variants accelerates GRIN variants stratification |
title | Identification of homologous GluN subunits variants accelerates GRIN variants stratification |
title_full | Identification of homologous GluN subunits variants accelerates GRIN variants stratification |
title_fullStr | Identification of homologous GluN subunits variants accelerates GRIN variants stratification |
title_full_unstemmed | Identification of homologous GluN subunits variants accelerates GRIN variants stratification |
title_short | Identification of homologous GluN subunits variants accelerates GRIN variants stratification |
title_sort | identification of homologous glun subunits variants accelerates grin variants stratification |
topic | Cellular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816381/ https://www.ncbi.nlm.nih.gov/pubmed/36619673 http://dx.doi.org/10.3389/fncel.2022.998719 |
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