Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian population.

Bochra Ben Rhouma, Manuel Kley, Fakhri Kallabi, Faten Hadj Kacem, Thouraya Kammoun, Wajdi Safi, Leila Keskes, Mouna Mnif, Alex Odermatt, Neila Belguith

The Journal of steroid biochemistry and molecular biology 2023 Mar

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17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) converts Δ4-androstene-3,17-dione (androstenedione) to testosterone. It is expressed almost exclusively in the testes and is essential for appropriate male sexual development. More than 70 mutations in the HSD17B3 gene that cause 17β-HSD3 deficiency and result in 46,XY Disorders of Sex Development (46,XY DSD) have been reported. This study describes three novel Tunisian cases with mutations in HSD17B3. The first patient is homozygous for the previously reported mutation p.C206X. The inheritance of this mutation seemed to be independent of consanguineous marriage, which can be explained by its high frequency in the Tunisian population. The second patient has a novel splice site mutation in intron 6 at position c.490 -6 T > C. A splicing assay revealed a complete omission of exon 7 in the resulting HSD17B3 mRNA transcript. Skipping of exon 7 in HSD17B3 is predicted to cause a frame shift in exon 8 that affects the catalytic site and results in a truncation in exon 9, leading to an inactive enzyme. The third patient is homozygous for the novel missense mutation p.K202M, representing the first mutation identified in the catalytic tetrad of 17β-HSD3. Site-directed mutagenesis and enzyme activity measurements revealed a completely abolished 17β-HSD3 activity of the p.K202M mutant, despite unaffected protein expression, compared to the wild-type enzyme. Furthermore, the present study emphasizes the importance of genetic counselling, detabooization of 46,XY DSD, and a sensitization of the Tunisian population for the risks of consanguineous marriage. Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Citation

Bochra Ben Rhouma, Manuel Kley, Fakhri Kallabi, Faten Hadj Kacem, Thouraya Kammoun, Wajdi Safi, Leila Keskes, Mouna Mnif, Alex Odermatt, Neila Belguith. Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian population. The Journal of steroid biochemistry and molecular biology. 2023 Mar;227:106235