Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations
| Autor: | Menabò, Soara, Polat, Seher, Baldazzi, Lilia, Kulle, Alexandra E., Holterhus, Paul-Martin, Grötzinger, Joachim, Fanelli, Flaminia, Balsamo, Antonio, Riepe, Felix G. |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
Male
Models Molecular Adolescent Adrenal Hyperplasia Congenital Protein Conformation DNA Mutational Analysis Molecular Sequence Data Correction Cell Line Enzyme Activation Kinetics Young Adult Adrenal Cortex Hormones Mutation Genetics Humans Steroid 11-beta-Hydroxylase Female Amino Acid Sequence Child Sequence Alignment Genetic Association Studies Genetics (clinical) |
| Zdroj: | European Journal of Human Genetics. 28:692-692 |
| ISSN: | 1476-5438 1018-4813 |
| DOI: | 10.1038/s41431-020-0587-y |
| Popis: | Congenital adrenal hyperplasia (CAH) is one of the most common autosomal recessive inherited endocrine disease. Steroid 11β-hydroxylase deficiency (11β-OHD) is the second most common form of CAH. The aim of the study was to study the functional consequences of three novel and one previously described CYP11B1 gene mutations (p.(Arg143Trp), p.(Ala306Val), p.(Glu310Lys) and p.(Arg332Gln)) detected in patients suffering from classical and non-classical 11β-OHD. Functional analyses were performed by using a HEK293 cell in vitro expression system comparing wild type (WT) with mutant 11β-hydroxylase activity. Mutant proteins were examined in silico to study their effect on the three-dimensional structure of the protein. Two mutations (p.(Ala306Val) and p.(Glu310Lys)) detected in patients with classical 11β-OHD showed a nearly complete loss of 11β-hydroxylase activity. The mutations p.(Arg143Trp) and p.(Arg332Gln) detected in patients with non-classical 11β-OHD showed a partial functional impairment with approximately 8% and 6% of WT activity, respectively. Functional mutation analysis allows the classification of novel CYP11B1 mutations as causes of classical and non-classical 11β-OHD. The detection of patients with non-classical phenotypes underscores the importance to screen patients with a phenotype comparable to non-classical 21-hydroxylase deficiency for mutations in the CYP11B1 gene in case of a negative analysis of the CYP21A2 gene. As CYP11B1 mutations are most often individual for a family, the in vitro analysis of novel mutations is essential for clinical and genetic counselling. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full text from SpringerLink