| Literature DB >> 30067310 |
Rajini Sreenivasan1,2, Louisa Ludbrook1,3, Brett Fisher1,3, Faustine Declosmenil4, Kevin C Knower1, Brittany Croft1,5, Anthony D Bird1, Janelle Ryan1, Anu Bashamboo6, Andrew H Sinclair7, Peter Koopman8, Ken McElreavey6, Francis Poulat5, Vincent R Harley1,3,9.
Abstract
Nuclear receptor subfamily 5 group A member 1/Steroidogenic factor 1 (NR5A1; SF-1; Ad4BP) mutations cause 46,XY disorders of sex development (DSD), with phenotypes ranging from developmentally mild (e.g., hypospadias) to severe (e.g., complete gonadal dysgenesis). The molecular mechanism underlying this spectrum is unclear. During sex determination, SF-1 regulates SOX9 (SRY [sex determining region Y]-box 9) expression. We hypothesized that SF-1 mutations in 46,XY DSD patients affect SOX9 expression via the Testis-specific Enhancer of Sox9 core element, TESCO. Our objective was to assess the ability of 20 SF-1 mutants found in 46,XY DSD patients to activate TESCO. Patient DNA was sequenced for SF-1 mutations and mutant SF-1 proteins were examined for transcriptional activity, protein expression, sub-cellular localization and in silico structural defects. Fifteen of the 20 mutants showed reduced SF-1 activation on TESCO, 11 with atypical sub-cellular localization. Fourteen SF-1 mutants were predicted in silico to alter DNA, ligand or cofactor interactions. Our study may implicate aberrant SF-1-mediated transcriptional regulation of SOX9 in 46,XY DSDs.Entities:
Keywords: DSD; SF-1; SOX9; sex determination; testis-specific enhancer of SOX9
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Year: 2018 PMID: 30067310 DOI: 10.1002/humu.23603
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878