A Novel Missense Mutation in the HSD3B2 Gene, Underlying Nonsalt-Wasting Congenital Adrenal Hyperplasia. New Insight Into the Structure-Function Relationships of 3 beta-Hydroxysteroid Dehidrogenase Type II

作者：Sonia Baquedano Maria; Ciaccio Marta; Marino Roxana; Perez Garrido Natalia; Ramirez Pablo; Maceiras Mercedes; Turjanski Adrian; Defelipe Lucas A; Rivarola Marco A; Belgorosky Alicia^*

来源：Journal of Clinical Endocrinology & Metabolism, 2015, 100(1): E191-E196.

DOI：10.1210/jc.2014-2676

Context: 3 beta HSD2 is a bifunctional microsomal NAD(+)-dependent enzyme crucial for adrenal and gonad steroid biosynthesis, converting Delta 5-steroids to Delta 4-steroids. 3 beta HSD2 deficiency is a rare cause of congenital adrenal hyperplasia caused by recessive loss-of-function HSD3B2 mutations.
Objective: The aim was to define the pathogenic consequences of a novel missense mutation in the HSD3B2 gene.
Patient: We report a 7-month-old 46, XX girl referred because of precocious pubarche and postnatal clitoromegaly. Hormonal profile showed inadequate glucocorticoid levels, increased 17OHP and renin levels, and very high DHEAS levels, suggestive of compensated nonsalt-losing 3 beta HSD2 deficiency.
Design and Results: Direct sequencing revealed a novel, homozygous, pG250V HSD3B2 mutation. In vitro analysis in intact COS-7 cells showed impaired enzymatic activity for the conversion of pregnenolone to progesterone and dehydroepiandrosterone to androstenedione (20% and 27% of WT at 6 h, respectively). G250V-3 beta HSD2 decreased the V-max for progesterone synthesis without affecting the Km for pregnenolone. Western blot and immunofluorescence suggested that p.G250V mutation has no effect on the expression and intracellular localization of the mutant protein. Molecular homology modeling predicted that mutant V250 affected an L239-Q251 loop next to a beta-sheet structure in the NAD+-binding domain.
Conclusions: We identified a novel p.G250V mutation of HSD3B2 which causes an incomplete loss of enzymatic activity, explaining the compensated nonsalt loss phenotype. In vitro and in silico experiments provided insight into the structure-function relationship of the 3 beta HSD2 protein suggesting the importance of the L239-Q251 loop for the catalytic activity of the otherwise stable 3 beta HSD2 enzyme.

• 出版日期2015-1