Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Department of Pediatric Nephrology, School of Medicine, Tokyo Women's Medical University, Tokyo, Japan.
J Hum Genet. 2019 Jul;64(7):673-679. doi: 10.1038/s10038-019-0606-4. Epub 2019 Apr 23.
Advances in molecular genetics have revealed that approximately 30% of cases with steroid-resistant nephrotic syndrome (SRNS) are caused by single-gene mutations. More than 50 genes are responsible for SRNS. One such gene is the nucleoporin, 93-KD (NUP93). Thus far, few studies have reported mutations of NUP93 in SRNS. Here, we describe an NUP93 biallelic mutation in a 9-year-old boy with focal segmental glomerular sclerosis (FSGS). Notably, one mutation comprised an intronic variant; we conducted in vivo and in vitro analysis to characterize this variant. We found two heterozygous mutations in NUP93: c.2137-18G>A in intron 19 and a novel nonsense mutation c.727A>T (p.Lys243*) in exon 8. We conducted RNA sequencing and in vitro splicing assays by using minigene construction, combined with protein expression analysis to determine the pathogenicity of the intronic variant. Both RNA sequencing and in vitro splicing assay showed exon 20-skipping by the intronic variant. In protein expression analysis, aberrant subcellular localization with small punctate vesicles in the cytoplasm was observed for the intronic variant. Taken together, we concluded that c.2137-18G>A was linked to pathogenicity due to aberrant splicing. NUP93 variants are quite rare; however, we have shown that even intronic variants in NUP93 can cause SRNS. This study provides a fundamental approach to validate the intronic variant, as well as new insights regarding the clinical spectrum of SRNS caused by rare gene variants.
分子遗传学的进展表明,大约 30%的类固醇抵抗性肾病综合征 (SRNS) 病例是由单基因突变引起的。超过 50 个基因与 SRNS 有关。其中一个基因是核孔蛋白 93-KD (NUP93)。到目前为止,很少有研究报道 NUP93 突变与 SRNS 有关。在这里,我们描述了一名 9 岁男孩局灶节段性肾小球硬化 (FSGS) 中 NUP93 的双等位基因突变。值得注意的是,其中一个突变是内含子变异;我们进行了体内和体外分析来描述这个变异。我们在 NUP93 中发现了两个杂合突变:第 19 内含子的 c.2137-18G>A 和外显子 8 中的一个新的无义突变 c.727A>T (p.Lys243*)。我们通过构建小基因进行 RNA 测序和体外剪接分析,并结合蛋白质表达分析来确定内含子变异的致病性。RNA 测序和体外剪接分析均显示内含子变异导致外显子 20 跳跃。在蛋白质表达分析中,观察到内含子变异导致异常的亚细胞定位,细胞质中出现小的点状囊泡。综上所述,我们得出结论,由于异常剪接,c.2137-18G>A 与致病性有关。NUP93 变异非常罕见;然而,我们已经表明,即使是 NUP93 的内含子变异也可以导致 SRNS。本研究为验证内含子变异提供了一种基本方法,并为罕见基因变异引起的 SRNS 的临床谱提供了新的见解。