GRIN2A Gene

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1		Dean Liu	+ 616 word(s)	616	2020-12-15 07:55:27

This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/grin2a

Glutamate ionotropic receptor NMDA type subunit 2A

genes

1. Introduction

The GRIN2A gene provides instructions for making a protein called GluN2A (formerly known as NR2A). This protein is found in nerve cells (neurons) in the brain and spinal cord, including regions of the brain involved in speech and language. The GluN2A protein is one component (subunit) of a subset of NMDA receptors. There are several types of NMDA receptors, made up of different combinations of protein components. NMDA receptors are glutamate-gated ion channels; when brain chemicals called glutamate and glycine attach to the receptor, a channel opens, allowing positively charged particles (cations) to flow through. The flow of cations generates currents that activate (excite) neurons to send signals in the brain. NMDA receptors are involved in normal brain development, changes in the brain in response to experience (synaptic plasticity), learning, and memory. They also appear to play a role during deep (slow-wave) sleep.

The GluN2A subunit of NMDA receptors determines where in the brain the receptor is located and how it functions. It also provides the site to which glutamate binds.

2. Health Conditions Related to Genetic Changes

2.1. Epilepsy-aphasia spectrum

More than 50 mutations in the GRIN2A gene have been identified in some people with conditions that fall along the epilepsy-aphasia spectrum. This group of conditions is characterized by abnormal electrical activity in the brain, usually during slow-wave sleep; a loss of speech and language skills and sometimes other developmental skills; and in many cases, recurrent seizures (epilepsy). Landau-Kleffner syndrome (LKS) and epileptic encephalopathy with continuous spike-and-wave during sleep (ECSWS) are at the severe end of the spectrum, while childhood epilepsy with centrotemporal spikes (CECTS) is at the mild end. Several other conditions have signs and symptoms of intermediate severity.

Many GRIN2A gene mutations lead to production of a nonfunctional GluN2A protein or prevent the production of any protein at all. These mutations likely lead to a reduced number of NMDA receptors containing the GluN2A subunit. Researchers suspect that, as a result, signaling occurs through other types of NMDA receptors that more easily excite neurons, leading to excessive signaling in the brain. Other mutations lead to production of abnormal GluN2A proteins that likely alter how the NMDA receptors function, possibly increasing signaling. Excessive activity of neurons in the brain can lead to seizures and other abnormal brain activity and may result in death of the neurons. Changes in GluN2A appear to specifically affect signaling in regions of the brain involved in speech and language and disrupt brain activity during slow-wave sleep, leading to several of the signs and symptoms of this group of conditions. It is not clear why some GRIN2A gene mutations lead to a relatively mild condition and others cause more severe signs and symptoms.

2.2. Other disorders

GRIN2A gene mutations have been found in people with neurological disorders that have features similar to epilepsy-aphasia spectrum disorders (described above) but lacking consistent language problems. These shared features can include recurrent seizures (epilepsy), often of a type that originates from abnormal activity in the rolandic region of the brain (rolandic epilepsy); intellectual disability; and developmental delay. Some people with mutations in chromosome 16 that delete the GRIN2A gene as well as other nearby genes also have unusual facial features. The varying effects of different GRIN2A gene mutations and how they contribute to different neurological disorders are under study.

3. Other Names for This Gene

EPND
GluN2A
glutamate receptor ionotropic, NMDA 2A isoform 1 precursor
glutamate receptor ionotropic, NMDA 2A isoform 2 precursor
glutamate receptor, ionotropic, N-methyl D-aspartate 2A
LKS
N-methyl D-aspartate receptor subtype 2A
N-methyl-D-aspartate receptor channel, subunit epsilon-1
N-methyl-D-aspartate receptor subunit 2A
NMDAR2A
NR2A

References

Burnashev N, Szepetowski P. NMDA receptor subunit mutations inneurodevelopmental disorders. Curr Opin Pharmacol. 2015 Feb;20:73-82. doi:10.1016/j.coph.2014.11.008.
Carvill GL, Regan BM, Yendle SC, O'Roak BJ, Lozovaya N, Bruneau N, BurnashevN, Khan A, Cook J, Geraghty E, Sadleir LG, Turner SJ, Tsai MH, Webster R, OuvrierR, Damiano JA, Berkovic SF, Shendure J, Hildebrand MS, Szepetowski P, SchefferIE, Mefford HC. GRIN2A mutations cause epilepsy-aphasia spectrum disorders. NatGenet. 2013 Sep;45(9):1073-6. doi: 10.1038/ng.2727.
Lemke JR, Lal D, Reinthaler EM, Steiner I, Nothnagel M, Alber M, Geider K,Laube B, Schwake M, Finsterwalder K, Franke A, Schilhabel M, Jähn JA, Muhle H,Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P,Larsen J, Møller RS, Hjalgrim H, Addis L, Tang S, Hughes E, Pal DK, Veri K, VaherU, Talvik T, Dimova P, Guerrero López R, Serratosa JM, Linnankivi T, LehesjokiAE, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J, Datta AN, Fiedler B, KurlemannG, Kluger G, Hahn A, Haberlandt DE, Kutzer C, Sperner J, Becker F, Weber YG,Feucht M, Steinböck H, Neophythou B, Ronen GM, Gruber-Sedlmayr U, Geldner J,Harvey RJ, Hoffmann P, Herms S, Altmüller J, Toliat MR, Thiele H, Nürnberg P,Wilhelm C, Stephani U, Helbig I, Lerche H, Zimprich F, Neubauer BA, Biskup S, vonSpiczak S. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandicspikes. Nat Genet. 2013 Sep;45(9):1067-72. doi: 10.1038/ng.2728.
Lesca G, Rudolf G, Bruneau N, Lozovaya N, Labalme A, Boutry-Kryza N, Salmi M, Tsintsadze T, Addis L, Motte J, Wright S, Tsintsadze V, Michel A, Doummar D,Lascelles K, Strug L, Waters P, de Bellescize J, Vrielynck P, de Saint Martin A, Ville D, Ryvlin P, Arzimanoglou A, Hirsch E, Vincent A, Pal D, Burnashev N,Sanlaville D, Szepetowski P. GRIN2A mutations in acquired epileptic aphasia andrelated childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nat Genet. 2013 Sep;45(9):1061-6. doi: 10.1038/ng.2726.
Paoletti P. Molecular basis of NMDA receptor functional diversity. Eur JNeurosci. 2011 Apr;33(8):1351-65. doi: 10.1111/j.1460-9568.2011.07628.x.
Reutlinger C, Helbig I, Gawelczyk B, Subero JI, Tönnies H, Muhle H,Finsterwalder K, Vermeer S, Pfundt R, Sperner J, Stefanova I, Gillessen-Kaesbach G, von Spiczak S, van Baalen A, Boor R, Siebert R, Stephani U, Caliebe A.Deletions in 16p13 including GRIN2A in patients with intellectual disability,various dysmorphic features, and seizure disorders of the rolandic region.Epilepsia. 2010 Sep;51(9):1870-3. doi: 10.1111/j.1528-1167.2010.02555.x.
Turner SJ, Mayes AK, Verhoeven A, Mandelstam SA, Morgan AT, Scheffer IE.GRIN2A: an aptly named gene for speech dysfunction. Neurology. 2015 Feb10;84(6):586-93. doi: 10.1212/WNL.0000000000001228.
Wyllie DJ, Livesey MR, Hardingham GE. Influence of GluN2 subunit identity onNMDA receptor function. Neuropharmacology. 2013 Nov;74:4-17. doi:10.1016/j.neuropharm.2013.01.016.

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Subjects: Genetics & Heredity

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Dean Liu

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Entry Collection: MedlinePlus

Update Date: 22 Dec 2020

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