Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Pathology and Laboratory Medicine, The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, PA 19104, USA; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Am J Hum Genet. 2024 Aug 8;111(8):1656-1672. doi: 10.1016/j.ajhg.2024.06.011. Epub 2024 Jul 22.
Pathogenic variants in the JAG1 gene are a primary cause of the multi-system disorder Alagille syndrome. Although variant detection rates are high for this disease, there is uncertainty associated with the classification of missense variants that leads to reduced diagnostic yield. Consequently, up to 85% of reported JAG1 missense variants have uncertain or conflicting classifications. We generated a library of 2,832 JAG1 nucleotide variants within exons 1-7, a region with a high number of reported missense variants, and designed a high-throughput assay to measure JAG1 membrane expression, a requirement for normal function. After calibration using a set of 175 known or predicted pathogenic and benign variants included within the variant library, 486 variants were characterized as functionally abnormal (n = 277 abnormal and n = 209 likely abnormal), of which 439 (90.3%) were missense. We identified divergent membrane expression occurring at specific residues, indicating that loss of the wild-type residue itself does not drive pathogenicity, a finding supported by structural modeling data and with broad implications for clinical variant classification both for Alagille syndrome and globally across other disease genes. Of 144 uncertain variants reported in patients undergoing clinical or research testing, 27 had functionally abnormal membrane expression, and inclusion of our data resulted in the reclassification of 26 to likely pathogenic. Functional evidence augments the classification of genomic variants, reducing uncertainty and improving diagnostics. Inclusion of this repository of functional evidence during JAG1 variant reclassification will significantly affect resolution of variant pathogenicity, making a critical impact on the molecular diagnosis of Alagille syndrome.
JAG1 基因中的致病变异是多系统疾病 Alagille 综合征的主要原因。尽管该疾病的变异检测率很高,但由于导致诊断率降低的错义变异分类存在不确定性,因此高达 85%的报告 JAG1 错义变异具有不确定或相互矛盾的分类。我们在exon 1-7 内生成了 2832 个 JAG1 核苷酸变异的文库,这是一个有大量报道的错义变异的区域,并设计了一种高通量测定法来测量 JAG1 膜表达,这是正常功能的要求。使用包括在变异文库中的一组 175 个已知或预测的致病性和良性变异进行校准后,有 486 个变异被鉴定为功能异常(n=277 个异常和 n=209 个可能异常),其中 439 个(90.3%)为错义。我们发现特定残基处存在不同的膜表达,这表明野生型残基的丢失本身并不驱动致病性,这一发现得到了结构建模数据的支持,对 Alagille 综合征和全球其他疾病基因的临床变异分类具有广泛的影响。在接受临床或研究检测的患者中,有 144 个不确定的变异报告,其中 27 个具有异常的膜表达,我们的数据的纳入导致其中 26 个被重新分类为可能致病性。功能证据增强了基因组变异的分类,减少了不确定性并改善了诊断。在 JAG1 变异重新分类期间纳入该功能证据库将显著影响变异致病性的确定,对 Alagille 综合征的分子诊断产生重大影响。