Skip to Main content Skip to Navigation
Journal articles

A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism

Abstract : Primary aldosteronism is the most common and curable form of secondary arterial hypertension. We performed whole-exome sequencing in patients with early-onset primary aldosteronism and identified a de novo heterozygous c.71G>A/p.Gly24Asp mutation in the CLCN2 gene, encoding the voltage-gated ClC-2 chloride channel 1 , in a patient diagnosed at 9 years of age. Patch-clamp analysis of glomerulosa cells of mouse adrenal gland slices showed hyperpolarization-activated Cl- currents that were abolished in Clcn2-/- mice. The p.Gly24Asp variant, located in a well-conserved 'inactivation domain'2,3, abolished the voltage- and time-dependent gating of ClC-2 and strongly increased Cl- conductance at resting potentials. Expression of ClC-2Asp24 in adrenocortical cells increased expression of aldosterone synthase and aldosterone production. Our data indicate that CLCN2 mutations cause primary aldosteronism. They highlight the important role of chloride in aldosterone biosynthesis and identify ClC-2 as the foremost chloride conductor of resting glomerulosa cells.
Complete list of metadata

Cited literature [3 references]  Display  Hide  Download
Contributor : Fabio Fernandes Rosa Connect in order to contact the contributor
Submitted on : Wednesday, April 3, 2019 - 11:38:46 AM
Last modification on : Wednesday, October 20, 2021 - 12:17:38 AM


Files produced by the author(s)



Fabio Fernandes-Rosa, Georgios Daniil, Ian Orozco, Corinna Göppner, Rami El Zein, et al.. A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism. Nature Genetics, Nature Publishing Group, 2018, 50 (3), pp.355-361. ⟨10.1038/s41588-018-0053-8⟩. ⟨inserm-02088868⟩



Record views


Files downloads