Journal Article

Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

Schwarzmayr, Thomas, Fischer, Evelyn, Graf, Elisabeth, Boulkroun, Sheerazed, Amar, Laurence, Meitinger, Thomas, Lichtenauer, Urs D, Tauber, Philipp, Osswald, Andrea, Strom, Tim M, Vilsen, Bente, Quinkler, Marcus, Schack, Vivien R, Samson-Couterie, Benoit, Allolio, Bruno, Warth, Richard, Walther, Anett, Mulatero, Paolo, Jeunemaitre, Xavier, Diener, Susanne, Wieland, Thomas, Benecke, Arndt, Fallo, Francesco, Mantero, Franco, Beuschlein, Felix, Plouin, Pierre-Francois, Nielsen, Hang N, Penton, David, Zennaro, Maria-Christina, Reincke, Martin

2013

Overview

Felix Beuschlein, Martin Reincke and colleagues identify recurrent somatic mutations in ATP1A1 and ATP2B3 in aldosterone-producing adenomas with wild-type KCNJ5 . The ATP1A1 and ATP2B3 mutations alter conserved residues and lead to impaired sodium, potassium and calcium ion homeostasis. Primary aldosteronism is the most prevalent form of secondary hypertension. To explore molecular mechanisms of autonomous aldosterone secretion, we performed exome sequencing of aldosterone-producing adenomas (APAs). We identified somatic hotspot mutations in the ATP1A1 (encoding an Na + /K + ATPase α subunit) and ATP2B3 (encoding a Ca 2+ ATPase) genes in three and two of the nine APAs, respectively. These ATPases are expressed in adrenal cells and control sodium, potassium and calcium ion homeostasis. Functional in vitro studies of ATP1A1 mutants showed loss of pump activity and strongly reduced affinity for potassium. Electrophysiological ex vivo studies on primary adrenal adenoma cells provided further evidence for inappropriate depolarization of cells with ATPase alterations. In a collection of 308 APAs, we found 16 (5.2%) somatic mutations in ATP1A1 and 5 (1.6%) in ATP2B3 . Mutation-positive cases showed male dominance, increased plasma aldosterone concentrations and lower potassium concentrations compared with mutation-negative cases. In summary, dominant somatic alterations in two members of the ATPase gene family result in autonomous aldosterone secretion.

• Publisher: Nature Publishing Group US,Nature Publishing Group
• Subject: 631/208/2489/144 / 631/443/592/75/243 / 631/45/776/775 / 631/67 / Adrenal Cortex Neoplasms - etiology / Adrenocortical Adenoma - etiology / Agriculture / Aldosterone - metabolism / Amino acids / Animal Genetics and Genomics / Biomedicine / Calcium - metabolism / Cancer Research / Cells, Cultured / Diagnosis / Electrophysiology / Gene Function / Gene mutations / Genetic aspects / Health aspects / Heart attacks / Human Genetics / Humans / Hyperaldosteronism / Hypertension / Hypertension - etiology / Identification and classification / Immunoenzyme Techniques / letter / Life Sciences / Mutation / Mutation - genetics / Neurons and Cognition / Plasma Membrane Calcium-Transporting ATPases - genetics / Potassium - metabolism / Proteins / Risk factors / Rodents / Sodium - metabolism / Sodium-Potassium-Exchanging ATPase - genetics / Tumors