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Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome
Daniela A. Braun, … , Mustafa K. Khokha, Friedhelm Hildebrandt
Daniela A. Braun, … , Mustafa K. Khokha, Friedhelm Hildebrandt
Published September 4, 2018
Citation Information: J Clin Invest. 2018;128(10):4313-4328. https://doi.org/10.1172/JCI98688.
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Research Article Genetics Nephrology

Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome

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Abstract

Steroid-resistant nephrotic syndrome (SRNS) almost invariably progresses to end-stage renal disease. Although more than 50 monogenic causes of SRNS have been described, a large proportion of SRNS remains unexplained. Recently, it was discovered that mutations of NUP93 and NUP205, encoding 2 proteins of the inner ring subunit of the nuclear pore complex (NPC), cause SRNS. Here, we describe mutations in genes encoding 4 components of the outer rings of the NPC, namely NUP107, NUP85, NUP133, and NUP160, in 13 families with SRNS. Using coimmunoprecipitation experiments, we showed that certain pathogenic alleles weakened the interaction between neighboring NPC subunits. We demonstrated that morpholino knockdown of nup107, nup85, or nup133 in Xenopus disrupted glomerulogenesis. Re-expression of WT mRNA, but not of mRNA reflecting mutations from SRNS patients, mitigated this phenotype. We furthermore found that CRISPR/Cas9 knockout of NUP107, NUP85, or NUP133 in podocytes activated Cdc42, an important effector of SRNS pathogenesis. CRISPR/Cas9 knockout of nup107 or nup85 in zebrafish caused developmental anomalies and early lethality. In contrast, an in-frame mutation of nup107 did not affect survival, thus mimicking the allelic effects seen in humans. In conclusion, we discovered here that mutations in 4 genes encoding components of the outer ring subunits of the NPC cause SRNS and thereby provide further evidence that specific hypomorphic mutations in these essential genes cause a distinct, organ-specific phenotype.

Authors

Daniela A. Braun, Svjetlana Lovric, David Schapiro, Ronen Schneider, Jonathan Marquez, Maria Asif, Muhammad Sajid Hussain, Ankana Daga, Eugen Widmeier, Jia Rao, Shazia Ashraf, Weizhen Tan, C. Patrick Lusk, Amy Kolb, Tilman Jobst-Schwan, Johanna Magdalena Schmidt, Charlotte A. Hoogstraten, Kaitlyn Eddy, Thomas M. Kitzler, Shirlee Shril, Abubakar Moawia, Kathrin Schrage, Arwa Ishaq A. Khayyat, Jennifer A. Lawson, Heon Yung Gee, Jillian K. Warejko, Tobias Hermle, Amar J. Majmundar, Hannah Hugo, Birgit Budde, Susanne Motameny, Janine Altmüller, Angelika Anna Noegel, Hanan M. Fathy, Daniel P. Gale, Syeda Seema Waseem, Ayaz Khan, Larissa Kerecuk, Seema Hashmi, Nilufar Mohebbi, Robert Ettenger, Erkin Serdaroğlu, Khalid A. Alhasan, Mais Hashem, Sara Goncalves, Gema Ariceta, Mercedes Ubetagoyena, Wolfram Antonin, Shahid Mahmood Baig, Fowzan S. Alkuraya, Qian Shen, Hong Xu, Corinne Antignac, Richard P. Lifton, Shrikant Mane, Peter Nürnberg, Mustafa K. Khokha, Friedhelm Hildebrandt

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Figure 5

A truncating mutation but not a hypomorphic mutation of nup107 causes early lethality and developmental defects in zebrafish.

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A truncating mutation but not a hypomorphic mutation of nup107 causes ea...
Zebrafish lines with mutations of nup107 were generated using CRISPR/Cas9 technology. Lethality following het × het in-crossing was monitored twice daily over the indicated periods. Genotyping was performed in all fish and was compatible with Mendelian ratios. (A) Kaplan-Meier survival curves of 86 larvae demonstrate that homozygous (hom) larvae carrying the frameshift mutation p.Thr81Argfs*74 of nup107 died before 5 dpf, contrary to heterozygous (het) and wild-type (WT) controls (n = 26 hom, 39 het, 21 WT). (B) Kaplan-Meier survival curves of a zebrafish line carrying a hypomorphic mutation of nup107 (p.Ala46delAla). Note that, contrary to the truncating allele, this in-frame deletion of nup107 does not impair survival of homozygous larvae compared with WT fish or heterozygous clutch mates (n = 14 hom, 27 het, 15 WT). (C–G) Phenotypes of homozygous nup107-knockout larvae (p.Thr81Argfs*74) on day 4 dpf. Specifically, the phenotype included small eyes, ventral body axis curvature, and peripheral as well as periorbital edema. (C and D) Yellow circumferences drawn around the pigmented area of the eyes of knockout fish (C) versus heterozygous clutch mates (D) assess eye size using ImageJ. (E) Quantification of eye size measurements (see C and D) demonstrates significantly smaller eyes in homozygous fish compared with heterozygous or WT clutch mates. One-way ANOVA with a standard confidence interval of 95% results in F(2, 84) = 84.72; P < 0.0001. Two-tailed P values (Šidák’s multiple-comparisons test) are shown in the figure (****P < 0.001). (F) Representative image showing ventral body axis curvature in a homozygous knockout fish. (G) Representative image displaying body and periorbital edema in a homozygous knockout fish. For quantification of F and G, see Table 2. Scale bars in C, D, F, and G: 500 μm.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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