Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences

Hum Genet. 1987 Nov;77(3):236-40. doi: 10.1007/BF00284476.

Abstract

The parental origin of five X isochromosomes were determined using 11 DNA markers. The isochromosome was derived from a maternal X chromosome in three cases and from a paternal X chromosome in two. Unexpected heterozygosity was detected for the proximal Xp region in one individual in whom the i(Xq) chromosome was paternally derived. This was confirmed by in situ hybridisation. A mode of formation of isochromosomes by breakage and reunion between the sister chromatids of the arms of an X chromosome is proposed to account for this. Sister chromatid breakage and reunion can be considered as a significant mechanism for the origin of i(Xq) chromosomes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Aberrations*
  • Chromosome Banding
  • DNA / genetics*
  • Female
  • Genetic Markers
  • Humans
  • Karyotyping
  • Male
  • Meiosis
  • Models, Genetic
  • Nucleic Acid Hybridization
  • Polymorphism, Genetic*
  • Turner Syndrome / genetics*
  • X Chromosome*

Substances

  • Genetic Markers
  • DNA