Department of Pediatrics, Xiangya Hospital of Central South University, Changsha, Hunan Province, China.
Department of Physical Medicine & Rehabilitation, Xiangya Hospital of Central South University, Changsha, Hunan Province, China.
J Hum Genet. 2023 Jun;68(6):375-382. doi: 10.1038/s10038-023-01128-2. Epub 2023 Feb 7.
U2 small nuclear RNA auxiliary factor 2 (U2AF2) is an indispensable pre-mRNA splicing factor in the early process of splicing. Recently, U2AF2 was reported as a novel candidate gene associated with neurodevelopmental disorders. Herein, we report a patient with a novel presumed heterozygous missense variant in the U2AF2 gene (c.603G>T), who has a similar clinical phenotype as the patient reported before, including epilepsy, intellectual disability, language delay, microcephaly, and hypoplastic corpus callosum. We reviewed the phenotypic and genetic spectrum of patients with U2AF2-related neurological diseases, both newly diagnosed and previously reported. To investigate the possible pathogenesis, EBV-immortalized lymphoblastoid cells were derived from the peripheral blood obtained from the patient and control groups. Furthermore, according to the results of WB, RT-PCR, Q-PCR, and cDNA sequencing of RT-PCR products, the presumed missense variant c.603G>T caused exon 6 skipping in the U2AF2 mRNA transcript and led to a truncated protein (p.E163_E201del). Cell Counting Kit-8 (CCK-8) and cell cycle detection demonstrated that the variant c.603G>T inhibited the proliferation of patient lymphocyte cells compared with the control group. This study is aimed at expanding the phenotypic and genetic spectrum of U2AF2-related neurodevelopmental diseases and investigating the potential effects. This is the first report of the possible pathogenesis of a U2AF2 gene pathogenic variant in a patient with neurodevelopmental diseases and shows that a novel presumed missense variant in the U2AF2 gene causes exon skipping.
U2 小核 RNA 辅助因子 2(U2AF2)是剪接早期过程中必不可少的前体 mRNA 剪接因子。最近,U2AF2 被报道为一种与神经发育障碍相关的新候选基因。在此,我们报道了一名患者携带 U2AF2 基因(c.603G>T)的新型假定杂合错义变异,该患者具有与之前报道的患者相似的临床表型,包括癫痫、智力障碍、语言延迟、小头畸形和胼胝体发育不全。我们回顾了新诊断和以前报道的 U2AF2 相关神经疾病患者的表型和遗传谱。为了研究可能的发病机制,我们从患者和对照组的外周血中衍生出 EBV 永生化淋巴母细胞系。此外,根据 WB、RT-PCR、Q-PCR 和 RT-PCR 产物 cDNA 测序的结果,假定的错义变异 c.603G>T 导致 U2AF2 mRNA 转录本中第 6 外显子跳跃,导致截短蛋白(p.E163_E201del)。细胞计数试剂盒-8(CCK-8)和细胞周期检测表明,与对照组相比,变异 c.603G>T 抑制了患者淋巴细胞的增殖。本研究旨在扩大 U2AF2 相关神经发育疾病的表型和遗传谱,并研究潜在的影响。这是首例报道 U2AF2 基因致病性变异在神经发育疾病患者中可能的发病机制的研究,并表明 U2AF2 基因的一种新型假定错义变异导致外显子跳跃。