Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

Cited 259 time in scopus
Metadata Downloads
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability
F F Hamdan; J Gauthier; Y Araki; D T Lin; Y Yoshizawa; K Higashi; A-reum Park; D Spiegelman; S Dobrzeniecka; A Piton; H Tomitori; H Daoud; C Massicotte; E Henrion; O Diallo; M Shekarabi; C Marineau; M Shevell; B Maranda; G Mitchell; A Nadeau; G D'Anjou; M Vanasse; M Srour; R G Lafreniere; P Drapeau; J C Lacaille; E Kim; Jae-Ran Lee; K Igarashi; R L Huganir; G A Rouleau; J L Michaud
Bibliographic Citation
American Journal of Human Genetics, vol. 88, no. 3, pp. 306-316
Publication Year
Little is known about the genetics of nonsyndromic intellectual disability (NSID). We hypothesized that de novo mutations (DNMs) in synaptic genes explain an important fraction of sporadic NSID cases. In order to investigate this possibility, we sequenced 197 genes encoding glutamate receptors and a large subset of their known interacting proteins in 95 sporadic cases of NSID. We found 11 DNMs, including ten potentially deleterious mutations (three nonsense, two splicing, one frameshift, four missense) and one neutral mutation (silent) in eight different genes. Calculation of point-substitution DNM rates per functional and neutral site showed significant excess of functional DNMs compared to neutral ones. De novo truncating and/or splicing mutations in SYNGAP1, STXBP1, and SHANK3 were found in six patients and are likely to be pathogenic. De novo missense mutations were found in KIF1A, GRIN1, CACNG2, and EPB41L1. Functional studies showed that all these missense mutations affect protein function in cell culture systems, suggesting that they may be pathogenic. Sequencing these four genes in 50 additional sporadic cases of NSID identified a second DNM in GRIN1 (c.1679-1681dup/p.Ser560dup). This mutation also affects protein function, consistent with structural predictions. None of these mutations or any other DNMs were identified in these genes in 285 healthy controls. This study highlights the importance of the glutamate receptor complexes in NSID and further supports the role of DNMs in this disorder.
Elsevier-Cell Press
Appears in Collections:
Division of Biomedical Research > Rare Disease Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.

Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.