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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.
Nat Commun. 2019 07 12; 10(1):3094.NC

Abstract

AMPA receptors (AMPARs) are tetrameric ligand-gated channels made up of combinations of GluA1-4 subunits encoded by GRIA1-4 genes. GluA2 has an especially important role because, following post-transcriptional editing at the Q607 site, it renders heteromultimeric AMPARs Ca2+-impermeable, with a linear relationship between current and trans-membrane voltage. Here, we report heterozygous de novo GRIA2 mutations in 28 unrelated patients with intellectual disability (ID) and neurodevelopmental abnormalities including autism spectrum disorder (ASD), Rett syndrome-like features, and seizures or developmental epileptic encephalopathy (DEE). In functional expression studies, mutations lead to a decrease in agonist-evoked current mediated by mutant subunits compared to wild-type channels. When GluA2 subunits are co-expressed with GluA1, most GRIA2 mutations cause a decreased current amplitude and some also affect voltage rectification. Our results show that de-novo variants in GRIA2 can cause neurodevelopmental disorders, complementing evidence that other genetic causes of ID, ASD and DEE also disrupt glutamatergic synaptic transmission.

Authors+Show Affiliations

Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto "Giannina Gaslini", 16147, Genoa, Italy. Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16132, Genoa, Italy.Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, 98195, USA. Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410083, Hunan, China.Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Pediatric Neurology Unit, Safra Children's Hospital, Sheba Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, 526121, Ramat Gan, Israel.Centre de Référence des Malformations et Maladies Congénitales du Cervelet, Département de Génétique et Embryologie Médicale, APHP, Hôpital Trousseau, 75012, Paris, France.Centre de Référence des Malformations et Maladies Congénitales du Cervelet, Service de Neurologie Pédiatrique, APHP, Hôpital Trousseau, 75012, Paris, France.GeneDx, Gaithersburg, MD, 20877, USA.Biochemistry Center, Heidelberg University, D-69120, Heidelberg, Germany.Royal Devon and Exeter NHS Foundation Trust, Exeter, EX1 2ED, UK.Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Department of Biochemistry and Genetics, University Hospital, 49933, Angers, France. MitoLab, UMR CNRS 6015-INSERM U1083, MitoVasc Institute, Angers University, 49100, Angers, France.Department of Biochemistry and Genetics, University Hospital, 49933, Angers, France. MitoLab, UMR CNRS 6015-INSERM U1083, MitoVasc Institute, Angers University, 49100, Angers, France.Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto "Giannina Gaslini", 16147, Genoa, Italy. Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16132, Genoa, Italy.Great Ormond Street Hospital for Children, London, WC1N 3JH, UK.Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Division of Medical Genetics, Northwell Health/Hofstra University SOM, New York, 11020, USA.Division of Medical Genetics, Northwell Health/Hofstra University SOM, New York, 11020, USA.Department of Clinical and Movement Neurosciences and Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, London, WC1N 1PJ, UK.Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.Department of Medical Sciences, Medical Genetics Unit, University of Torino, 10126, Torino, Italy.Department of Medical Sciences, Medical Genetics Unit, University of Torino, 10126, Torino, Italy.Department of Public Health and Pediatrics, University of Torino, 10126, Torino, Italy.Unit of Medical and Molecular Genetics, University Hospital Sant Joan de Deu Barcelona, 08950, Barcelona, Spain.Unit of Neuropediatrics, University Hospital, Angers Cedex, 49933, France.Pediatric Neurology Unit, Safra Children's Hospital, Sheba Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, 526121, Ramat Gan, Israel.Pediatric Neurology Unit, Safra Children's Hospital, Sheba Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, 526121, Ramat Gan, Israel.GeneDx, Gaithersburg, MD, 20877, USA.GeneDx, Gaithersburg, MD, 20877, USA.GeneDx, Gaithersburg, MD, 20877, USA.GeneDx, Gaithersburg, MD, 20877, USA.GeneDx, Gaithersburg, MD, 20877, USA.Department of Biomedical Sciences, Seoul National University, Seoul, 03080, South Korea.Department of Pediatrics, Seoul National University, Seoul, 03080, South Korea.Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410083, Hunan, China.Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410083, Hunan, China.Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, 98195, USA. Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410083, Hunan, China.Department of Psychiatry, University of Washington, Seattle, WA, 98195, USA.Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410083, Hunan, China.Center for Autism and Related Disorders, Kennedy Krieger Institute, Baltimore, Maryland, 21211, USA.Center for Autism and Related Disorders, Kennedy Krieger Institute, Baltimore, Maryland, 21211, USA.Department of Clinical Genetics, University of Amsterdam, Meibergdreef 9, 1105, Amsterdam, Netherlands.Department of Pediatric Neurology, Amsterdam UMC, 1105, Amsterdam, Netherlands.Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Melbourne, Victoria, 3084, Australia.Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Melbourne, Victoria, 3084, Australia.Department of Pediatrics, University of Washington, Seattle, WA, 98195, USA.Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, WA, 98195, USA.Department of Clinical Genomics, Mayo Clinic, Rochester, 55902, MN, USA.Department of Clinical Genomics, Mayo Clinic, Rochester, 55902, MN, USA.Department of Clinical Genomics, Mayo Clinic, Rochester, 55902, MN, USA.Department of Clinical Genomics, Mayo Clinic, Rochester, 55902, MN, USA.Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, K1H 8L1, Canada.Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, K1H 8L1, Canada. Department of Human Genetics, McGill University Health Centre, Montréal, QC, H4A 3J1, Canada. Genome Québec Innovation Center, Montréal, QC, H3A 0G1, Canada.Child and Adolescent Psychiatry Department, Hospital General Universitario Gregorio Marañón, School of Medicine, Universidad Complutense, IiSGM, CIBERSAM, 28007, Madrid, Spain.Institute of Psychiatry and Mental Health, Hospital General Universitario Gregorio Maranon, Universidad Complutense, CIBERSAM, 28007, Madrid, Spain.Hospital Gregorio Maranon, IiSGM, School of Medicine, Calle Dr Esquerdo, 46, 28007, Madrid, Spain.Grupo de Medicina Xenómica, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), CIMUS, Universidade de Santiago de Compostela, 15782, Santiago de Compostela, Spain. Fundación Pública Galega de Medicina Xenómica- IDIS- Servicio Galego de Saúde (SERGAS), 15706, 15782, Santiago de Compostela, Spain.Department of Clinical Genetics, Leiden University Medical Center, 2333 ZA, Leiden, Netherlands.Department of Clinical Genetics, Leiden University Medical Center, 2333 ZA, Leiden, Netherlands.Department of Genetics, Assistance Publique - Hôpitaux de Paris, University Hôpital Pitié-Salpêtrière, 75013, Paris, France.Department of Genetics, Assistance Publique - Hôpitaux de Paris, University Hôpital Pitié-Salpêtrière, 75013, Paris, France.Department of Health Promotion,Mother and Child Care, Internal Medicine and Medical Specialities "G. D'Alessandro", University of Palermo, 90133, Palermo, Italy.Laboratory of Neurogenetics and Neuroscience, IRCCS Istituto "Giannina Gaslini", 16147, Genova, Italy.Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto "Giannina Gaslini", 16147, Genoa, Italy. Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16132, Genoa, Italy.Institute for Maternal and Child Health, IRCCS "Burlo Garofolo", University of Trieste, 34134, Trieste, Italy.Institute for Maternal and Child Health, IRCCS "Burlo Garofolo", University of Trieste, 34134, Trieste, Italy.No affiliation info availableDepartment of Pediatric Neurology, University Hospital Vall d'Hebron, Universitat Autònoma de Barcelona, 08035, Barcelona, Spain.Neuroscience Medical Group, 1625 Stockton Boulevard, Suite 104, Sacramento, CA, 95816, USA.Department of Genetics and Inherited Metabolic diseases, Children's Hospital Colorado, Aurora, CO, 80045, USA.Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.William Greenleaf Eliot Division of Child & Adolescent Psychiatry, Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, 63110, USA.Department of Chemical and Pharmaceutical Sciences, University of Trieste, 34134, Trieste, Italy.Department of Chemical and Pharmaceutical Sciences, University of Trieste, 34134, Trieste, Italy.Neurogenetics Unit, Department of Neurology, University of Sao Paulo, Sao Paulo, 01308-000, Brazil. Mendelics Genomic Analysis, Sao Paulo, SP, 04013-000, Brazil.Department of Genetics, Assistance Publique - Hôpitaux de Paris, University Hôpital Pitié-Salpêtrière, 75013, Paris, France.Department of Biochemistry and Genetics, University Hospital, 49933, Angers, France. MitoLab, UMR CNRS 6015-INSERM U1083, MitoVasc Institute, Angers University, 49100, Angers, France.Department of Biomedical Sciences, Seoul National University, Seoul, 03080, South Korea.Pediatric Neurology Unit, Safra Children's Hospital, Sheba Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, 526121, Ramat Gan, Israel.Laboratory of Neurogenetics and Neuroscience, IRCCS Istituto "Giannina Gaslini", 16147, Genova, Italy.Department of Pediatrics, University of Washington, Seattle, WA, 98195, USA.Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Melbourne, Victoria, 3084, Australia.Centre for Genomic Medicine, Manchester Academic Health Sciences Centre, Central Manchester University Hospitals NHS Foundation Trust, Lancashire, M13 9WL, UK. Division of Evolution and Genomic Sciences, School of Biological Sciences, University of Manchester, Manchester, M13 9WL, UK.Department of Pediatric Neurology, University Hospital Vall d'Hebron, Universitat Autònoma de Barcelona, 08035, Barcelona, Spain.Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Department of Cell Biology, Yale University School of Medicine, New Haven, CT, 06520, USA.Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, 98195, USA. Howard Hughes Medical Institute, University of Washington, Seattle, WA, 98195, USA.Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. d.kullmann@ucl.ac.uk.Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. h.houlden@ucl.ac.uk.

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Video-Audio Media

Language

eng

PubMed ID

31300657

Citation

Salpietro, Vincenzo, et al. "AMPA Receptor GluA2 Subunit Defects Are a Cause of Neurodevelopmental Disorders." Nature Communications, vol. 10, no. 1, 2019, p. 3094.
Salpietro V, Dixon CL, Guo H, et al. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. Nat Commun. 2019;10(1):3094.
Salpietro, V., Dixon, C. L., Guo, H., Bello, O. D., Vandrovcova, J., Efthymiou, S., Maroofian, R., Heimer, G., Burglen, L., Valence, S., Torti, E., Hacke, M., Rankin, J., Tariq, H., Colin, E., Procaccio, V., Striano, P., Mankad, K., Lieb, A., ... Houlden, H. (2019). AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. Nature Communications, 10(1), 3094. https://doi.org/10.1038/s41467-019-10910-w
Salpietro V, et al. AMPA Receptor GluA2 Subunit Defects Are a Cause of Neurodevelopmental Disorders. Nat Commun. 2019 07 12;10(1):3094. PubMed PMID: 31300657.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. AU - Salpietro,Vincenzo, AU - Dixon,Christine L, AU - Guo,Hui, AU - Bello,Oscar D, AU - Vandrovcova,Jana, AU - Efthymiou,Stephanie, AU - Maroofian,Reza, AU - Heimer,Gali, AU - Burglen,Lydie, AU - Valence,Stephanie, AU - Torti,Erin, AU - Hacke,Moritz, AU - Rankin,Julia, AU - Tariq,Huma, AU - Colin,Estelle, AU - Procaccio,Vincent, AU - Striano,Pasquale, AU - Mankad,Kshitij, AU - Lieb,Andreas, AU - Chen,Sharon, AU - Pisani,Laura, AU - Bettencourt,Conceicao, AU - Männikkö,Roope, AU - Manole,Andreea, AU - Brusco,Alfredo, AU - Grosso,Enrico, AU - Ferrero,Giovanni Battista, AU - Armstrong-Moron,Judith, AU - Gueden,Sophie, AU - Bar-Yosef,Omer, AU - Tzadok,Michal, AU - Monaghan,Kristin G, AU - Santiago-Sim,Teresa, AU - Person,Richard E, AU - Cho,Megan T, AU - Willaert,Rebecca, AU - Yoo,Yongjin, AU - Chae,Jong-Hee, AU - Quan,Yingting, AU - Wu,Huidan, AU - Wang,Tianyun, AU - Bernier,Raphael A, AU - Xia,Kun, AU - Blesson,Alyssa, AU - Jain,Mahim, AU - Motazacker,Mohammad M, AU - Jaeger,Bregje, AU - Schneider,Amy L, AU - Boysen,Katja, AU - Muir,Alison M, AU - Myers,Candace T, AU - Gavrilova,Ralitza H, AU - Gunderson,Lauren, AU - Schultz-Rogers,Laura, AU - Klee,Eric W, AU - Dyment,David, AU - Osmond,Matthew, AU - Parellada,Mara, AU - Llorente,Cloe, AU - Gonzalez-Peñas,Javier, AU - Carracedo,Angel, AU - Van Haeringen,Arie, AU - Ruivenkamp,Claudia, AU - Nava,Caroline, AU - Heron,Delphine, AU - Nardello,Rosaria, AU - Iacomino,Michele, AU - Minetti,Carlo, AU - Skabar,Aldo, AU - Fabretto,Antonella, AU - ,, AU - Raspall-Chaure,Miquel, AU - Chez,Michael, AU - Tsai,Anne, AU - Fassi,Emily, AU - Shinawi,Marwan, AU - Constantino,John N, AU - De Zorzi,Rita, AU - Fortuna,Sara, AU - Kok,Fernando, AU - Keren,Boris, AU - Bonneau,Dominique, AU - Choi,Murim, AU - Benzeev,Bruria, AU - Zara,Federico, AU - Mefford,Heather C, AU - Scheffer,Ingrid E, AU - Clayton-Smith,Jill, AU - Macaya,Alfons, AU - Rothman,James E, AU - Eichler,Evan E, AU - Kullmann,Dimitri M, AU - Houlden,Henry, Y1 - 2019/07/12/ PY - 2018/07/30/received PY - 2019/05/22/accepted PY - 2019/7/14/entrez PY - 2019/7/14/pubmed PY - 2019/10/28/medline SP - 3094 EP - 3094 JF - Nature communications JO - Nat Commun VL - 10 IS - 1 N2 - AMPA receptors (AMPARs) are tetrameric ligand-gated channels made up of combinations of GluA1-4 subunits encoded by GRIA1-4 genes. GluA2 has an especially important role because, following post-transcriptional editing at the Q607 site, it renders heteromultimeric AMPARs Ca2+-impermeable, with a linear relationship between current and trans-membrane voltage. Here, we report heterozygous de novo GRIA2 mutations in 28 unrelated patients with intellectual disability (ID) and neurodevelopmental abnormalities including autism spectrum disorder (ASD), Rett syndrome-like features, and seizures or developmental epileptic encephalopathy (DEE). In functional expression studies, mutations lead to a decrease in agonist-evoked current mediated by mutant subunits compared to wild-type channels. When GluA2 subunits are co-expressed with GluA1, most GRIA2 mutations cause a decreased current amplitude and some also affect voltage rectification. Our results show that de-novo variants in GRIA2 can cause neurodevelopmental disorders, complementing evidence that other genetic causes of ID, ASD and DEE also disrupt glutamatergic synaptic transmission. SN - 2041-1723 UR - https://www.unboundmedicine.com/medline/citation/31300657/AMPA_receptor_GluA2_subunit_defects_are_a_cause_of_neurodevelopmental_disorders L2 - http://dx.doi.org/10.1038/s41467-019-10910-w DB - PRIME DP - Unbound Medicine ER -