Combination of genetic studies and animal modeling proposes TMPRSS9 as a candidate gene for serum K+ variations

Sci Rep. 2025 Jul 12;15(1):25211. doi: 10.1038/s41598-025-11106-7.

Abstract

A candidate gene association analysis identified TMPRSS9 as gene for potassium sensitivity in women. To validate this finding, constitutive and conditional Tmprss9 knockout mice were generated and subjected to dietary K+ deprivation and K+ loading. Interestingly, mouse renal Tmprss9 gene expression was similar in both sexes on standard diet but differed when challenged with K+-deprivation or -loading in wildtype (WT) mice. Constitutive deficiency of Tmprss9 was evidenced on a transcriptional level in knockout (KO) mice. Serum Na+ levels were lower in male and female KO mice on low K+ (LKD), while on high K+ (HKD) diet, serum K+ only increased in male KO mice. Upon all diet conditions namely standard diet (SD), LKD and HKD the protein abundances of sodium transporting proteins like the sodium-chloride symporter (NCC), alpha and gamma epithelial sodium channel (ENaC) subunits as well as their ratio of cleaved/full length protein and the sodium-hydrogen exchanger 3 (NHE3) were similar in WT and KO mice and/or showed only minor differences. We propose that in human, TMPRSS9 may function as a sex-specific modifier gene for serum K+ handling in women, whereas in mice, male rather than female Tmprss9 KO retained serum K+ on HKD.

Keywords: Dietary potassium; Na+ handling; Proteases; Sex specificity; Variation in K+.

MeSH terms

  • Animals
  • Female
  • Genetic Association Studies
  • Humans
  • Male
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Mice
  • Mice, Knockout
  • Potassium* / blood
  • Serine Endopeptidases* / genetics
  • Serine Endopeptidases* / metabolism
  • Sodium / blood

Substances

  • Serine Endopeptidases
  • Membrane Proteins
  • Potassium
  • prostasin
  • Sodium