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簇集突变导致 GRIK2 型谷氨酸受体亚基基因异常,从而引发多种神经发育障碍。

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

机构信息

Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

Department of Genetics, University Medical Center Groningen, Groningen 9700, the Netherlands.

出版信息

Am J Hum Genet. 2021 Sep 2;108(9):1692-1709. doi: 10.1016/j.ajhg.2021.07.007. Epub 2021 Aug 9.

Abstract

Kainate receptors (KARs) are glutamate-gated cation channels with diverse roles in the central nervous system. Bi-allelic loss of function of the KAR-encoding gene GRIK2 causes a nonsyndromic neurodevelopmental disorder (NDD) with intellectual disability and developmental delay as core features. The extent to which mono-allelic variants in GRIK2 also underlie NDDs is less understood because only a single individual has been reported previously. Here, we describe an additional eleven individuals with heterozygous de novo variants in GRIK2 causative for neurodevelopmental deficits that include intellectual disability. Five children harbored recurrent de novo variants (three encoding p.Thr660Lys and two p.Thr660Arg), and four children and one adult were homozygous for a previously reported variant (c.1969G>A [p.Ala657Thr]). Individuals with shared variants had some overlapping behavioral and neurological dysfunction, suggesting that the GRIK2 variants are likely pathogenic. Analogous mutations introduced into recombinant GluK2 KAR subunits at sites within the M3 transmembrane domain (encoding p.Ala657Thr, p.Thr660Lys, and p.Thr660Arg) and the M3-S2 linker domain (encoding p.Ile668Thr) had complex effects on functional properties and membrane localization of homomeric and heteromeric KARs. Both p.Thr660Lys and p.Thr660Arg mutant KARs exhibited markedly slowed gating kinetics, similar to p.Ala657Thr-containing receptors. Moreover, we observed emerging genotype-phenotype correlations, including the presence of severe epilepsy in individuals with the p.Thr660Lys variant and hypomyelination in individuals with either the p.Thr660Lys or p.Thr660Arg variant. Collectively, these results demonstrate that human GRIK2 variants predicted to alter channel function are causative for early childhood development disorders and further emphasize the importance of clarifying the role of KARs in early nervous system development.

摘要

红藻氨酸受体 (KARs) 是谷氨酸门控阳离子通道,在中枢神经系统中具有多种作用。KAR 编码基因 GRIK2 的双等位基因功能丧失导致一种非综合征性神经发育障碍 (NDD),其核心特征为智力残疾和发育迟缓。单等位基因变异在 GRIK2 中是否也导致 NDD 尚不清楚,因为以前只报道过一个个体。在这里,我们描述了另外 11 个个体存在杂合新生变异的 GRIK2,这些变异导致神经发育缺陷,包括智力残疾。有 5 个儿童携带反复发生的新生变异(编码 p.Thr660Lys 的 3 个和 p.Thr660Arg 的 2 个),4 个儿童和 1 个成年人是以前报道的变异(c.1969G>A [p.Ala657Thr])的纯合子。具有共享变异的个体存在一些重叠的行为和神经功能障碍,这表明 GRIK2 变异可能是致病的。在重组 GluK2 KAR 亚基的 M3 跨膜结构域(编码 p.Ala657Thr、p.Thr660Lys 和 p.Thr660Arg)和 M3-S2 连接子域(编码 p.Ile668Thr)内引入类似的突变对同型和异型 KAR 的功能特性和膜定位具有复杂的影响。p.Thr660Lys 和 p.Thr660Arg 突变型 KAR 表现出明显减慢的门控动力学,类似于含有 p.Ala657Thr 的受体。此外,我们观察到出现了基因型-表型相关性,包括 p.Thr660Lys 变异的个体中存在严重的癫痫发作,以及 p.Thr660Lys 或 p.Thr660Arg 变异的个体中存在少突胶质细胞发育不全。总之,这些结果表明,预测改变通道功能的人类 GRIK2 变异是导致儿童早期发育障碍的原因,并进一步强调阐明 KAR 在早期神经系统发育中的作用的重要性。

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