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Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2
Arthritis Research & Therapy volume 21, Article number: 219 (2019)
Genetic dysfunction of ABCG2 is an important risk factor of familial early-onset hyperuricemia and gout.
We herein report the case of one European family with early onset of hyperuricemia/gout of which female proband was found to have pediatric-onset hyperuricemia associated with a newly identified functionally null variant allele in ATP-binding cassette transporter G2 (ABCG2). Hitherto, we and other groups revealed that the dysfunction of ABCG2—a physiologically important urate exporter expressed in the kidney and intestine—raises the risk of hyperuricemia/gout [1,2,3,4]; however, there is little information on this relationship in terms of familial history of early-onset hyperuricemia/gout. Our case will emphasize the importance of ABCG2 genotyping in the risk estimation of early onset of such excess urate-related diseases, which has the potential for clinical application in precision medicine.
The pedigree is depicted in Fig. 1a. Detailed information on each subject and related methods are available in Additional file 1. Metabolic investigation for purine metabolism suggested that hyperuricemia in two patients (the family proband II:2 and III:1) was not caused by excess production of uric acid, which led us to focus on the excretion system for urate from the body.
To explore the possible causes of this familial hyperuricemia/gout, we addressed ABCG2 genotypes in this family since dysfunction of ABCG2 is the strongest genetic risk factor of hyperuricemia/gout that affects urate excretion. As a result of targeted exon sequencing of ABCG2, two non-synonymous allelic variants of ABCG2—c.34G>A (p.V12 M) and c.725T>C (p.I242T, a novel variant)—were found in this family. There were no already-known genetic risk factors for hyperuricemia/gout such as ABCG2 c.376C>T (p.Q126X) and c.421C>A (p.Q141K). Given that p.V12M variant that was only found in the subject III:2 reportedly has no effects on the expression and urate transport activity of ABCG2 , we focused on the c.725T>C (p.I242T) in each subject (Fig. 1a). Heterozygous mutation at c.725 T>C was identified in all early-onset hyperuricemia/gout patients (II:2 and III:1) and one young girl (III:3). She has been on very strict purine/lactose/gluten diet for more than 10 years, which might suppress the elevation of her serum urate (sU) levels. Moreover, subjects I:2 (post-menopausal hyperuricemia woman) and III:2 (generally healthy man) who never showed clinical signs of early onset of hyperuricemia/gout were homozygous of ABCG2 wild-type. Thus, it is conceivable that ABCG2 c.725T>C (p.I242T) associated with the development of early onset of hyperuricemia/gout in this family.
Next, we experimentally investigated the effect of this novel non-synonymous mutation (p.I242T) on the intracellular processing and function of ABCG2 protein. A series of biochemical analyses using transiently ABCG2-expressing mammalian cells demonstrated that the p.I242T variant had little effect on the protein level and N-glycosylation status of ABCG2 (Fig. 1b) and that, like ABCG2 wild-type, matured-p.I242T variant localized on the plasma membrane as a glycoprotein (Fig. 1c, d). However, functional assay revealed that contrary to the wild-type, the p.I242T variant had no ATP-dependent urate transport activity (Fig. 1e). Moreover, a cell-based urate transport assay supported that the p.I242T variant could hardly excrete urate from cells to extracellular spaces (Additional file 1: Figure S1). Thus, we concluded that the ABCG2 p.I242T variant is functionally null as an ATP-dependent urate transporter. Considering that a conserved H243 (a neighbor of I242) coordinates the γ-phosphate of ATP together with Q211 and Q126 , structural modification caused by the local amino acid substitution (p.I242T) might affect ATP-driven conformational changes in ABCG2, resulting in the disruption of its transport activity.
In summary, we identified a novel functionally null variant of ABCG2 that related to the development of early onset of hyperuricemia/gout in a European pedigree. To the best of our knowledge, this is the first report of pedigree analysis through three generations supporting a positive relationship between familial hyperuricemia/gout history and dysfunctional allele of ABCG2.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
ATP-binding cassette transporter G2
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All authors are grateful to all the subjects who kindly took part in this study.
The present study was supported by the JSPS KAKENHI Grant Numbers 15H05610 and 19K16441 (to Y.T.); 16H1808 and 18KK0247 (to T.T.) as well as grants from the Czech Republic Ministry of Health AZV 15-26693 A and RVO VFN64165, RVO 00023728 to B.S.; T.T. has received research grants from the Gout Research Foundation, The Takeda Medical Foundation, and MSD Life Science Foundation, Public Interest Incorporated Foundation.
Ethics approval and consent to participate
This study was approved by the Ethics Committee of the Institute of Rheumatology in Prague (no.6181/2015). All patients and healthy controls were fully informed of the aim of the study, and written informed consent was obtained from all participants.
Consent for publication
Written informed consents were obtained from all subjects for publication of this case report.
The authors declare that they have no competing interests.
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Toyoda, Y., Pavelcová, K., Klein, M. et al. Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2. Arthritis Res Ther 21, 219 (2019) doi:10.1186/s13075-019-2007-7