Département de Génétique, Hôpital Robert-Debré, Paris, France.
Centre for Genomic and Experimental Medicine and Simons Initiative for the Developing Brain, Institute of Genetics and Cancer, Edinburgh, Scotland, UK.
Eur J Hum Genet. 2024 Sep;32(9):1144-1149. doi: 10.1038/s41431-024-01560-8. Epub 2024 Feb 15.
Translation elongation factor eEF1A2 constitutes the alpha subunit of the elongation factor-1 complex, responsible for the enzymatic binding of aminoacyl-tRNA to the ribosome. Since 2012, 21 pathogenic missense variants affecting EEF1A2 have been described in 42 individuals with a severe neurodevelopmental phenotype including epileptic encephalopathy and moderate to profound intellectual disability (ID), with neurological regression in some patients. Through international collaborative call, we collected 26 patients with EEF1A2 variants and compared them to the literature. Our cohort shows a significantly milder phenotype. 83% of the patients are walking (vs. 29% in the literature), and 84% of the patients have language skills (vs. 15%). Three of our patients do not have ID. Epilepsy is present in 63% (vs. 93%). Neurological examination shows a less severe phenotype with significantly less hypotonia (58% vs. 96%), and pyramidal signs (24% vs. 68%). Cognitive regression was noted in 4% (vs. 56% in the literature). Among individuals over 10 years, 56% disclosed neurocognitive regression, with a mean age of onset at 2 years. We describe 8 novel missense variants of EEF1A2. Modeling of the different amino-acid sites shows that the variants associated with a severe phenotype, and the majority of those associated with a moderate phenotype, cluster within the switch II region of the protein and thus may affect GTP exchange. In contrast, variants associated with milder phenotypes may impact secondary functions such as actin binding. We report the largest cohort of individuals with EEF1A2 variants thus far, allowing us to expand the phenotype spectrum and reveal genotype-phenotype correlations.
翻译延伸因子 eEF1A2 构成延伸因子-1 复合物的 α 亚基,负责氨酰-tRNA 与核糖体的酶结合。自 2012 年以来,在 42 名具有严重神经发育表型(包括癫痫性脑病和中度至重度智力障碍[ID])的个体中已描述了 21 种影响 EEF1A2 的致病性错义变异,一些患者出现神经退行性。通过国际合作呼吁,我们收集了 26 名 EEF1A2 变异患者,并将其与文献进行了比较。我们的队列显示出明显较轻的表型。83%的患者可以行走(文献中为 29%),84%的患者有语言技能(文献中为 15%)。我们的三名患者没有 ID。癫痫存在于 63%(文献中为 93%)的患者中。神经系统检查显示出较轻的表型,明显较少的张力减退(58%比 96%)和锥体束征(24%比 68%)。4%的患者出现认知能力下降(文献中为 56%)。在 10 岁以上的个体中,56%的人出现神经认知能力下降,发病年龄平均为 2 岁。我们描述了 EEF1A2 的 8 种新错义变异。不同氨基酸位点的建模表明,与严重表型相关的变异,以及与中度表型相关的大多数变异,聚集在蛋白质的开关 II 区域内,因此可能会影响 GTP 交换。相比之下,与较轻表型相关的变异可能会影响二级功能,如肌动蛋白结合。我们报告了迄今为止最大的 EEF1A2 变异个体队列,使我们能够扩展表型谱并揭示基因型-表型相关性。