학술논문

Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.
Document Type
Article
Source
Nature Genetics. Sep2013, Vol. 45 Issue 9, p1055-1060. 6p. 2 Diagrams, 1 Chart, 3 Graphs.
Subject
*SOMATIC mutation
*HYPERTENSION genetics
*ALDOSTERONE
*GLOMERULOSCLEROSIS
*ADENOSINE triphosphatase
*GENETIC code
Language
ISSN
1061-4036
Abstract
At least 5% of individuals with hypertension have adrenal aldosterone-producing adenomas (APAs). Gain-of-function mutations in KCNJ5 and apparent loss-of-function mutations in ATP1A1 and ATP2A3 were reported to occur in APAs. We find that KCNJ5 mutations are common in APAs resembling cortisol-secreting cells of the adrenal zona fasciculata but are absent in a subset of APAs resembling the aldosterone-secreting cells of the adrenal zona glomerulosa. We performed exome sequencing of ten zona glomerulosa-like APAs and identified nine with somatic mutations in either ATP1A1, encoding the Na+/K+ ATPase α1 subunit, or CACNA1D, encoding Cav1.3. The ATP1A1 mutations all caused inward leak currents under physiological conditions, and the CACNA1D mutations induced a shift of voltage-dependent gating to more negative voltages, suppressed inactivation or increased currents. Many APAs with these mutations were <1 cm in diameter and had been overlooked on conventional adrenal imaging. Recognition of the distinct genotype and phenotype for this subset of APAs could facilitate diagnosis. [ABSTRACT FROM AUTHOR]