AI Article Synopsis

  • Bartter syndrome is a rare genetic disorder affecting kidney function by impairing electrolyte reabsorption, leading to potentially fatal conditions like hyponatremia and dehydration, with type II linked to mutations in the KCNJ1 gene.
  • The study focused on identifying new, uncharacterized mutations in KCNJ1 that may cause disease by using genomic databases and advanced computational tools to analyze phenotypic and genomic data, particularly from the UK Biobank, NIH TOPMed, and ClinVar.
  • Two mutations were highlighted: G228E, which destabilizes the potassium channel ROMK and leads to its degradation, and T300R, which is resistant to ER degradation but shows impaired channel activity, suggesting that these findings can help

Article Abstract

Bartter syndrome is a group of rare genetic disorders that compromise kidney function by impairing electrolyte reabsorption. Left untreated, the resulting hyponatremia, hypokalemia, and dehydration can be fatal, and there is currently no cure. Bartter syndrome type II specifically arises from mutations in KCNJ1, which encodes the renal outer medullary potassium channel, ROMK. Over 40 Bartter syndrome-associated mutations in KCNJ1 have been identified, yet their molecular defects are mostly uncharacterized. Nevertheless, a subset of disease-linked mutations compromise ROMK folding in the endoplasmic reticulum (ER), which in turn results in premature degradation via the ER associated degradation (ERAD) pathway. To identify uncharacterized human variants that might similarly lead to premature degradation and thus disease, we mined three genomic databases. First, phenotypic data in the UK Biobank were analyzed using a recently developed computational platform to identify individuals carrying KCNJ1 variants with clinical features consistent with Bartter syndrome type II. In parallel, we examined genomic data in both the NIH TOPMed and ClinVar databases with the aid of Rhapsody, a verified computational algorithm that predicts mutation pathogenicity and disease severity. Subsequent phenotypic studies using a yeast screen to assess ROMK function-and analyses of ROMK biogenesis in yeast and human cells-identified four previously uncharacterized mutations. Among these, one mutation uncovered from the two parallel approaches (G228E) destabilized ROMK and targeted it for ERAD, resulting in reduced cell surface expression. Another mutation (T300R) was ERAD-resistant, but defects in channel activity were apparent based on two-electrode voltage clamp measurements in X. laevis oocytes. Together, our results outline a new computational and experimental pipeline that can be applied to identify disease-associated alleles linked to a range of other potassium channels, and further our understanding of the ROMK structure-function relationship that may aid future therapeutic strategies to advance precision medicine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695394PMC
http://dx.doi.org/10.1371/journal.pgen.1011051DOI Listing

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