Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency

التفاصيل البيبلوغرافية
العنوان: Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency
المؤلفون: Eugen J. Schoenle, Anna Biason-Lauber
المصدر: American journal of human genetics. 67(6)
سنة النشر: 2000
مصطلحات موضوعية: Steroidogenic factor 1, medicine.medical_specialty, endocrine system, Heterozygote, Mutant, Adrenal Gland Diseases, Mutation, Missense, Fushi Tarazu Transcription Factors, Receptors, Cytoplasmic and Nuclear, 030209 endocrinology & metabolism, Biology, Steroidogenic Factor 1, 03 medical and health sciences, Exon, 0302 clinical medicine, Mutant protein, Genes, Reporter, Internal medicine, Report, medicine, Adrenal insufficiency, Genetics, Missense mutation, Humans, Genetics(clinical), Amino Acid Sequence, Adrenocortical Insufficiency, Genetics (clinical), 030304 developmental biology, Regulation of gene expression, Homeodomain Proteins, 0303 health sciences, Base Sequence, Ovary, Puberty, Infant, DNA, medicine.disease, DNA-Binding Proteins, Endocrinology, Phenotype, Gene Expression Regulation, Child, Preschool, Female, Protein Binding, Transcription Factors
الوصف: Steroidogenic factor 1 (NR5A1/SF-1) plays an essential role in the development of the hypothalamic-pituitary-adrenal and hypothalamic-pituitary-gonadal axes, controlling expression of their many important genes. The recent description of a 46,XY patient bearing a mutation in the NR5A1 gene, causing male pseudohermaphroditism and adrenal failure, demonstrated the crucial role of SF-1 in male gonadal differentiation. The role of SF-1 in human ovarian development was, until now, unknown. We describe a phenotypically and genotypically normal girl, with signs and symptoms of adrenal insufficiency and no apparent defect in ovarian maturation, bearing a heterozygote G--T transversion in exon 4 of the NR5A1 gene that leads to the missense R255L in the SF-1 protein. The exchange does not interfere with protein translation and stability. Consistent with the clinical picture, R255L is transcriptionally inactive and has no dominant-negative activity. The inability of the mutant (MUT) NR5A1/SF-1 to bind canonical DNA sequences might offer a possible explanation for the failure of the mutant protein to transactivate target genes. This is the first report of a mutation in the NR5A1 gene in a genotypically female patient, and it suggests that NR5A1/SF-1 is not necessary for female gonadal development, confirming the crucial role of NR5A1/SF-1 in adrenal gland formation in both sexes.
تدمد: 0002-9297
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4816885a40e86ffe589493f3c5c25d5dTest
https://pubmed.ncbi.nlm.nih.gov/11038323Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....4816885a40e86ffe589493f3c5c25d5d
قاعدة البيانات: OpenAIRE