Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY

Hum Genet. 1992 Apr;89(1):23-8. doi: 10.1007/BF00207036.

Abstract

XX maleness is the most common condition in which testes develop in the absence of a cytogenetically detectable Y chromosome. Using molecular techniques, it is possible to detect Yp sequences in the majority of XX males. In this study, we could detect Y-specific sequences, including the sex-determining region of the Y chromosome (SRY), using fluorescence in situ hybridization. In 5 out of 6 previously unpublished XX males, SRY was translocated onto the terminal part of an X chromosome. This is the first report in which translocation of an SRY-bearing fragment to an X chromosome in XX males could be directly demonstrated.

MeSH terms

  • Adolescent
  • Adult
  • Blotting, Southern
  • DNA Probes / genetics
  • DNA-Binding Proteins / genetics*
  • Fluorescence
  • Humans
  • Male
  • Nuclear Proteins*
  • Nucleic Acid Hybridization
  • Sex Chromosome Aberrations / genetics*
  • Sex Determination Analysis*
  • Sex-Determining Region Y Protein
  • Transcription Factors*
  • Translocation, Genetic / genetics*
  • X Chromosome*
  • Y Chromosome

Substances

  • DNA Probes
  • DNA-Binding Proteins
  • Nuclear Proteins
  • SRY protein, human
  • Sex-Determining Region Y Protein
  • Transcription Factors