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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 2

Mutations of NUP107, NUP85, and NUP133 weaken protein-protein interactions within the NPC.

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Mutations of NUP107, NUP85, and NUP133 weaken protein-protein interactio...
(A) The published structure of the Y complex of the NPC (11) was used to determine the localization of amino acid residues that we found altered in individuals with SRNS. Left: The 3D structure of the Y complex (pdb: 5A9Q): NUP133 (dark blue), NUP107 (light green), NUP96 (light blue), SEC13 (orange), SEH1L (violet), NUP85 (light gray), NUP43 (dark green), NUP160 (yellow), and NUP37 (red). Inset on right: The 3D structure of the interface region between NUP107 and NUP133 (pdb: 3CQC). The C-terminal part of NUP85 could not be fully resolved experimentally; a gray area indicates its predicted position. Residues Ala477, Ala581, and Arg645 of NUP85 (gray) and Glu803 of NUP160 (yellow) are located within incompletely resolved areas, and their positions are estimated. Note that amino acid residues Tyr889 of NUP107 (light green) and Ser974 of NUP133 (dark blue) point toward the interaction interface. (B) N-terminally FLAG-tagged NUP107 wild-type (WT) or mutant cDNA was overexpressed in HEK293T cells. Coimmunoprecipitation (coIP) demonstrates that the missense mutation Tyr889Cys weakens the interaction with endogenous NUP133. (C) A coIP experiment using N-terminally FLAG-tagged WT or mutant NUP133 cDNA demonstrates that the missense mutation Ser974Arg weakens the interaction with endogenous NUP107. As expected based on structural data, the 2 other missense mutations (Arg231Gly and Leu1055Ser) do not alter the NUP107-NUP133 interaction. (D) N-terminally Myc-tagged WT or mutant NUP85 cDNA was overexpressed in HEK293T cells. CoIP using an antibody against endogenous NUP160 shows that the missense mutations Ala581Pro and Arg645Trp of NUP85 weaken the interaction between the 2 proteins. FL, full-length; MOCK, empty vector. CoIP experiments in B–D were confirmed in 3 independent experiments.

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

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