Department of Genetics and Reference Center for Developmental Disorders, Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, FHU G4-Génomique, Rouen, France.
Centre de Génétique Humaine, Université de Franche-Comté, CHU Besançon, Besançon, France.
Hum Mutat. 2022 Sep;43(9):1239-1248. doi: 10.1002/humu.24384. Epub 2022 May 17.
Cornelia de Lange syndrome (CdLS) is a clinically-recognizable rare developmental disorder. About 70% of patients carry a missense or loss-of-function pathogenic variant in the NIPBL gene. We hypothesized that some variants in the 5'-untranslated region (UTR) of NIPBL may create an upstream open reading frame (uORF), putatively leading to a loss of function. We searched for NIPBL 5'-UTR variants potentially introducing uORF by (i) reannotating NGS data of 102 unsolved CdLS patients and (ii) literature and variant databases search. We set up a green fluorescent protein (GFP) reporter assay and studied NIPBL expression in a lymphoblastoid cell line (LCL). We identified two variants introducing a novel ATG codon sequence in the 5'-UTR of NIPBL, both predicted to introduce uORF: a novel c.-457_-456delinsAT de novo mutation in a 15-year-old male with classic CdLS, and a c.-94C>T variant in a published family. Our reporter assay showed a significant decrease of GFP levels in both mutant contexts, with similar levels of messenger RNA (mRNA) as compared to wt constructs. Assessment of LCL of one patient showed consistent results with decreased NIPBL protein and unchanged mRNA levels. 5'-UTR uORF-introducing NIPBL variants may represent a rare source of pathogenic variants in unsolved CdLS patients.
Cornelia de Lange 综合征(CdLS)是一种具有临床特征的罕见发育障碍。约 70%的患者在 NIPBL 基因中携带错义或功能丧失的致病性变异。我们假设 NIPBL 的 5'-非翻译区(UTR)中的一些变异可能会产生一个上游开放阅读框(uORF),可能导致功能丧失。我们通过(i)重新注释 102 例未解决的 CdLS 患者的 NGS 数据,(ii)文献和变异数据库搜索,寻找可能引入 uORF 的 NIPBL 5'-UTR 变异。我们建立了一个绿色荧光蛋白(GFP)报告基因检测,研究了在淋巴母细胞系(LCL)中 NIPBL 的表达。我们在一个 15 岁的具有经典 CdLS 的男性中发现了一个新的 c.-457_-456delinsAT 移码突变,在一个已发表的家族中发现了一个 c.-94C>T 变异,这两个变异都在 NIPBL 的 5'-UTR 中引入了一个新的 ATG 密码子序列,均预测会引入 uORF。我们的报告基因检测显示,在两种突变情况下 GFP 水平显著下降,与 wt 构建体相比,信使 RNA(mRNA)水平相似。对一名患者的 LCL 进行评估显示,NIPBL 蛋白水平降低,mRNA 水平不变,结果一致。5'-UTR uORF 引入的 NIPBL 变异可能是未解决的 CdLS 患者中致病性变异的一个罕见来源。