Aix Marseille Univ, INSERM, MMG, Marseille, France.
Institut des Neurosciences de la Timone, Aix-Marseille Université and CNRS UMR7289, Marseille, France.
Eur J Hum Genet. 2020 Dec;28(12):1703-1713. doi: 10.1038/s41431-020-0659-z. Epub 2020 Jun 2.
While chromosome 1p36 deletion syndrome is one of the most common terminal subtelomeric microdeletion syndrome, 1p36 microduplications are rare events. Polymicrogyria (PMG) is a brain malformation phenotype frequently present in patients with 1p36 monosomy. The gene whose haploinsufficiency could cause this phenotype remains to be identified. We used high-resolution arrayCGH in patients with various forms of PMG in order to identify chromosomal variants associated to the malformation and characterized the genes included in these regions in vitro and in vivo. We identified the smallest case of 1p36 duplication reported to date in a patient presenting intellectual disability, microcephaly, epilepsy, and perisylvian polymicrogyria. The duplicated segment is intrachromosomal, duplicated in mirror and contains two genes: enolase 1 (ENO1) and RERE, both disrupted by the rearrangement. Gene expression analysis performed using the patient cells revealed a reduced expression, mimicking haploinsufficiency. We performed in situ hybridization to describe the developmental expression profile of the two genes in mouse development. In addition, we used in utero electroporation of shRNAs to show that Eno1 inactivation in the rat causes a brain development defect. These experiments allowed us to define the ENO1 gene as the most likely candidate to contribute to the brain malformation phenotype of the studied patient and consequently a candidate to contribute to the malformations of the cerebral cortex observed in patients with 1p36 monosomy.
虽然 1p36 缺失综合征是最常见的端粒下微缺失综合征之一,但 1p36 微重复是罕见事件。多小脑回(PMG)是 1p36 单体性患者中经常出现的脑畸形表型。导致这种表型的基因的单倍不足仍然有待确定。我们使用高分辨率 arrayCGH 对具有各种形式 PMG 的患者进行了研究,以鉴定与畸形相关的染色体变异,并对这些区域内的基因进行了体外和体内特征分析。我们在一名表现为智力障碍、小头畸形、癫痫和围侧多小脑回的患者中发现了迄今为止报道的最小的 1p36 重复病例。重复片段是染色体内的,镜像重复,并包含两个基因:烯醇酶 1(ENO1)和 RERE,这两个基因都被重排破坏。使用患者细胞进行的基因表达分析显示,表达减少,类似于单倍不足。我们进行了原位杂交,以描述这两个基因在小鼠发育中的发育表达谱。此外,我们使用体内电穿孔 shRNA 来表明,大鼠 Eno1 的失活会导致大脑发育缺陷。这些实验使我们能够将 ENO1 基因定义为最有可能导致研究患者脑畸形表型的候选基因,从而也可能导致 1p36 单体性患者观察到的大脑皮层畸形的候选基因。