NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development

Genet Med. 2017 Apr;19(4):367-376. doi: 10.1038/gim.2016.118. Epub 2016 Aug 4.

Abstract

Purpose: We aimed to identify the genetic cause in a cohort of 11 unrelated cases and two sisters with 46,XX SRY-negative (ovo)testicular disorders of sex development (DSD).

Methods: Whole-exome sequencing (n = 9), targeted resequencing (n = 4), and haplotyping were performed. Immunohistochemistry of sex-specific markers was performed on patients' gonads. The consequences of mutation were investigated using luciferase assays, localization studies, and RNA-seq.

Results: We identified a novel heterozygous NR5A1 mutation, c.274C>T p.(Arg92Trp), in three unrelated patients. The Arg92 residue is highly conserved and located in the Ftz-F1 region, probably involved in DNA-binding specificity and stability. There were no consistent changes in transcriptional activation or subcellular localization. Transcriptomics in patient-derived lymphocytes showed upregulation of MAMLD1, a direct NR5A1 target previously associated with 46,XY DSD. In gonads of affected individuals, ovarian FOXL2 and testicular SRY-independent SOX9 expression observed.

Conclusions: We propose NR5A1, previously associated with 46,XY DSD and 46,XX primary ovarian insufficiency, as a novel gene for 46,XX (ovo)testicular DSD. We hypothesize that p.(Arg92Trp) results in decreased inhibition of the male developmental pathway through downregulation of female antitestis genes, thereby tipping the balance toward testicular differentiation in 46,XX individuals. In conclusion, our study supports a role for NR5A1 in testis differentiation in the XX gonad.Genet Med 19 4, 367-376.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA-Binding Proteins / genetics*
  • Female
  • Gene Expression Profiling / methods*
  • Genetic Predisposition to Disease
  • Haplotypes
  • Humans
  • Male
  • Models, Molecular
  • Mutation, Missense
  • Nuclear Proteins / genetics*
  • Ovary / metabolism
  • Ovotesticular Disorders of Sex Development / genetics*
  • Ovotesticular Disorders of Sex Development / metabolism
  • Pedigree
  • Polymorphism, Single Nucleotide
  • Sequence Analysis, RNA / methods*
  • Steroidogenic Factor 1 / chemistry
  • Steroidogenic Factor 1 / genetics*
  • Steroidogenic Factor 1 / metabolism
  • Testis / metabolism
  • Transcription Factors / genetics*
  • Up-Regulation
  • Whole Exome Sequencing / methods*
  • Young Adult

Substances

  • DNA-Binding Proteins
  • MAMLD1 protein, human
  • NR5A1 protein, human
  • Nuclear Proteins
  • Steroidogenic Factor 1
  • Transcription Factors