Center for Medical Genetics, Ghent University Hospital, 9000 Ghent, Belgium; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, 9000 Ghent, Belgium.
UMR1231 GAD, Inserm - Université de Bourgogne, Dijon, France; Centre de Référence Maladies Rares "Anomalies du Développement et Syndromes Malformatifs", Centre de Génétique, FHU-TRANSLAD, CHU Dijon Bourgogne, 21000 Dijon, France.
Am J Hum Genet. 2023 May 4;110(5):790-808. doi: 10.1016/j.ajhg.2023.03.016. Epub 2023 Apr 17.
SRSF1 (also known as ASF/SF2) is a non-small nuclear ribonucleoprotein (non-snRNP) that belongs to the arginine/serine (R/S) domain family. It recognizes and binds to mRNA, regulating both constitutive and alternative splicing. The complete loss of this proto-oncogene in mice is embryonically lethal. Through international data sharing, we identified 17 individuals (10 females and 7 males) with a neurodevelopmental disorder (NDD) with heterozygous germline SRSF1 variants, mostly de novo, including three frameshift variants, three nonsense variants, seven missense variants, and two microdeletions within region 17q22 encompassing SRSF1. Only in one family, the de novo origin could not be established. All individuals featured a recurrent phenotype including developmental delay and intellectual disability (DD/ID), hypotonia, neurobehavioral problems, with variable skeletal (66.7%) and cardiac (46%) anomalies. To investigate the functional consequences of SRSF1 variants, we performed in silico structural modeling, developed an in vivo splicing assay in Drosophila, and carried out episignature analysis in blood-derived DNA from affected individuals. We found that all loss-of-function and 5 out of 7 missense variants were pathogenic, leading to a loss of SRSF1 splicing activity in Drosophila, correlating with a detectable and specific DNA methylation episignature. In addition, our orthogonal in silico, in vivo, and epigenetics analyses enabled the separation of clearly pathogenic missense variants from those with uncertain significance. Overall, these results indicated that haploinsufficiency of SRSF1 is responsible for a syndromic NDD with ID due to a partial loss of SRSF1-mediated splicing activity.
SRSF1(也称为 ASF/SF2)是一种非小核核糖核蛋白(非-snRNP),属于精氨酸/丝氨酸(R/S)结构域家族。它识别并结合 mRNA,调节组成型和选择性剪接。在小鼠中,这种原癌基因的完全缺失是胚胎致死的。通过国际数据共享,我们鉴定了 17 名(10 名女性和 7 名男性)具有神经发育障碍(NDD)的个体,他们携带杂合性生殖系 SRSF1 变体,主要是从头发生的,包括三个移码变体、三个无义变体、七个错义变体和两个微缺失位于 17q22 区内,包含 SRSF1。只有在一个家庭中,不能确定新发生的起源。所有个体都表现出复发性表型,包括发育迟缓、智力障碍(DD/ID)、低张力、神经行为问题,伴有可变的骨骼(66.7%)和心脏(46%)异常。为了研究 SRSF1 变体的功能后果,我们进行了计算机结构建模,在果蝇中开发了体内剪接测定,并对受影响个体的血液衍生 DNA 进行了 episignature 分析。我们发现,所有失活功能和 7 个错义变体中的 5 个是致病性的,导致果蝇中 SRSF1 剪接活性丧失,与可检测和特异的 DNA 甲基化 episignature 相关。此外,我们的正交计算机、体内和表观遗传学分析能够将明确的致病性错义变体与具有不确定意义的变体区分开来。总之,这些结果表明,SRSF1 的单倍不足是导致 ID 伴发的综合征性 NDD 的原因,这是由于 SRSF1 介导的剪接活性部分丧失。