Biochemical analyses and molecular modeling explain the functional loss of 17β-hydroxysteroid dehydrogenase 3 mutant G133R in three Tunisian patients with 46, XY Disorders of Sex Development. Issue 155 (January 2016)

• Record Type: Journal Article
• Authors: Engeli, Roger T.; Rhouma, Bochra Ben; Sager, Christoph P.; Tsachaki, Maria; Birk, Julia; Fakhfakh, Faiza; Keskes, Leila; Belguith, Neila; Odermatt, Alex
• Is Part Of: Journal of steroid biochemistry and molecular biology. Issue 155 Part A(2016)
• Page Start: 147
• Page End: 154
• Publication Date: 2016-01
• Subjects: 46, XY DSD -- 17β-hydroxysteroid dehydrogenase -- HSD17B3 -- Testosterone -- Mutation -- Structure function relationship -- Male sexual development; Steroid hormones -- Periodicals; Biochemistry -- Periodicals; Hormones -- Periodicals; Molecular Biology -- Periodicals; Hormones stéroïdes -- Périodiques; Steroid hormones; Periodicals; 572.579
• DOI: 10.1016/j.jsbmb.2015.10.023
• Languages: English
• ISSNs: 0960-0760

Abstract

Highlights: A novel mutation in the HSD17B3 gene causing the substitution G133R was identified in three Tunisian patients with 46, XY DSD. Mutation G133R in 17β-HSD3 results in almost complete loss of enzyme activity. 17β-HSD3 mutant G133R is normally expressed and exhibits an ER membrane localization pattern. G133 is highly conserved among 17β-HSD enzymes and other SDRs. Site-directed mutagenesis and molecular modeling suggest that mutation to an arginine at position 133 interferes with binding of cofactor NADPH. Abstract: Mutations in the HSD17B3 gene resulting in 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) deficiency cause 46, XY Disorders of Sex Development (46, XY DSD). Approximately 40 different mutations in HSD17B3 have been reported; only few mutant enzymes have been mechanistically investigated. Here, we report novel compound heterozygous mutations in HSD17B3, composed of the nonsense mutation C206X and the missense mutation G133R, in three Tunisian patients from two non-consanguineous families. Mutants C206X and G133R were constructed by site-directed mutagenesis and expressed in HEK-293 cells. The truncated C206X enzyme, lacking part of the substrate binding pocket, was moderately expressed and completely lost its enzymatic activity. Wild-type 17β-HSD3 and mutant G133R showed comparable expression levels and intracellular localization. The conversion of Δ4-androstene-3, 17-dione (androstenedione) to testosterone was almost completely abolished for mutant G133R compared with wild-type 17β-HSD3. To obtain further mechanistic insight, G133 was mutated to alanine, phenylalanine and glutamine. G133Q and G133F were almost completely inactive, whereas G133A displayed about 70% of wild-type activity. Sequence analysis revealed that G133 on 17β-HSD3 is located in a motif highly conserved in 17β-HSDs and other short-chain dehydrogenase/reductase (SDR) enzymes. A homology model of 17β-HSD3 predicted that arginine or any other bulky residue at position 133 causes steric hindrance of cofactor NADPH binding, whereas substrate binding seems to be unaffected. The results indicate an essential role of G133 in the arrangement of the cofactor binding pocket, thus explaining the loss-of-function of 17β-HSD3 mutant G133R in the patients investigated.