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Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases
Yong Li, et al.
Yong Li, et al.
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Research Article Genetics Nephrology

Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases

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Abstract

Uromodulin (UMOD) is a major risk gene for monogenic and complex forms of kidney disease. The encoded kidney-specific protein uromodulin is highly abundant in urine and related to chronic kidney disease, hypertension, and pathogen defense. To gain insights into potential systemic roles, we performed genome-wide screens of circulating uromodulin using complementary antibody-based and aptamer-based assays. We detected 3 and 10 distinct significant loci, respectively. Integration of antibody-based results at the UMOD locus with functional genomics data (RNA-Seq, ATAC-Seq, Hi-C) of primary human kidney tissue highlighted an upstream variant with differential accessibility and transcription in uromodulin-synthesizing kidney cells as underlying the observed cis effect. Shared association patterns with complex traits, including chronic kidney disease and blood pressure, placed the PRKAG2 locus in the same pathway as UMOD. Experimental validation of the third antibody-based locus, B4GALNT2, showed that the p.Cys466Arg variant of the encoded N-acetylgalactosaminyltransferase had a loss-of-function effect leading to higher serum uromodulin levels. Aptamer-based results pointed to enzymes writing glycan marks present on uromodulin and to their receptors in the circulation, suggesting that this assay permits investigating uromodulin’s complex glycosylation rather than its quantitative levels. Overall, our study provides insights into circulating uromodulin and its emerging functions.

Authors

Yong Li, Yurong Cheng, Francesco Consolato, Guglielmo Schiano, Michael R. Chong, Maik Pietzner, Ngoc Quynh H. Nguyen, Nora Scherer, Mary L. Biggs, Marcus E. Kleber, Stefan Haug, Burulça Göçmen, Marie Pigeyre, Peggy Sekula, Inga Steinbrenner, Pascal Schlosser, Christina B. Joseph, Jennifer A. Brody, Morgan E. Grams, Caroline Hayward, Ulla T. Schultheiss, Bernhard K. Krämer, Florian Kronenberg, Annette Peters, Jochen Seissler, Dominik Steubl, Cornelia Then, Matthias Wuttke, Winfried März, Kai-Uwe Eckardt, Christian Gieger, Eric Boerwinkle, Bruce M. Psaty, Josef Coresh, Peter J. Oefner, Guillaume Pare, Claudia Langenberg, Jürgen E. Scherberich, Bing Yu, Shreeram Akilesh, Olivier Devuyst, Luca Rampoldi, Anna Köttgen

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Figure 7

B4GALNT2 and uromodulin expression analysis.

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B4GALNT2 and uromodulin expression analysis.
(A) RT-qPCR analysis of B4g...
(A) RT-qPCR analysis of B4galnt2 expression in isolated mouse nephron segments. Bars indicate mean ± SEM. n ≥ 3 fractions. Glom, glomerulus; PCT, proximal convoluted tubule; PST, proximal straight tubule; TAL, thick ascending limb; DCT, distal convoluted tubule; CD, collecting duct. (B) Upper panels: Immunofluorescence analysis showing UMOD (green) and B4GALNT2 (red) on paraffin-embedded kidney sections from WT mice (n = 2). Right panels show high-magnification pictures of UMOD-positive and UMOD-negative tubules. Nuclei are counterstained with DAPI. Lower panels: Immunofluorescence analysis showing AQP2 (green) and B4GALNT2 (red) on mouse kidney, showing a strong signal in the intercalated cells of collecting ducts. Right panels show high-magnification pictures of AQP2- and B4GALNT2-positive tubules. Nuclei are counterstained with DAPI. (C) Immunofluorescence analysis showing UMOD (green) and B4GALNT2 (red) on paraffin-embedded kidney sections from a normal human kidney. Right panels show high-magnification pictures of UMOD-positive and UMOD-negative tubules. Nuclei are counterstained with DAPI. (D) Western blot analysis showing uromodulin and B4GALNT2 in lysates of MDCK cell clones expressing UMOD with or without B4GALNT2 (see Methods), untreated or after deglycosylation with PNGase F. Actin is shown as a normalizer.

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ISSN 2379-3708

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