| Literature DB >> 31015583 |
Rini Rossanti1, Akemi Shono1, Kenichiro Miura2, Motoshi Hattori2, Tomohiko Yamamura1, Keita Nakanishi1, Shogo Minamikawa1, Junya Fujimura1, Tomoko Horinouchi1, China Nagano1, Nana Sakakibara1, Hiroshi Kaito1, Hiroaki Nagase1, Naoya Morisada1, Katsuhiko Asanuma3, Masafumi Matsuo4, Kandai Nozu5, Kazumoto Iijima1.
Abstract
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.Entities:
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Year: 2019 PMID: 31015583 DOI: 10.1038/s10038-019-0606-4
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172