The origin of the extra Y chromosome in males with a 47,XYY karyotype

Hum Mol Genet. 1999 Nov;8(12):2205-9. doi: 10.1093/hmg/8.12.2205.

Abstract

The presence of an extra Y chromosome in males is a relatively common occurrence, the 47,XYY karyotype being found in approximately 1 in 1000 male births. The error of disjunction must occur either during paternal meiosis II or as a post-zygotic mitotic error, both of which are rare events for other chromosomes. It is therefore of interest to determine when errors of Y chromosome disjunction occur. It is possible to distinguish between the different mechanisms of non-disjunction by analysing DNA polymorphisms at the distal tip of the Xp/Yp pseudoautosomal region in 47,XYY males, their parents and in some cases paternal grandparents. A cohort of 28 non-mosaic 47,XYY males was analysed. The results show that there are at least two mechanisms causing non-disjunction of the Y chromosome. In 16 of the 19 cases from which parents were available, the extra Y was generated by non-disjunction at meiosis II after a normal chiasmate meiosis I. Three cases were due to either a post-zygotic mitotic error or non-disjunction at meiosis II after a nullichiasmate meiosis I. Of the nine cases with no parental DNA available, at least four were due to meiosis II non-disjunction following a normal chiasmate meiosis I.

MeSH terms

  • Base Sequence
  • DNA Primers
  • Female
  • Humans
  • Karyotyping
  • Male
  • Pedigree
  • Sex Chromosome Aberrations*
  • Trisomy*
  • Y Chromosome*

Substances

  • DNA Primers