Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3

Nucleic Acids Res. 1987 Mar 25;15(6):2639-51. doi: 10.1093/nar/15.6.2639.

Abstract

We report the identification of a new RFLP detected by the DNA probe MN12, which is linked to both the fragile site on the X chromosome at Xq27.3 and the highly polymorphic locus detected by St14 (DXS52). In situ mapping confirms the localisation of MN12 distal to the fragile site. A detailed physical analysis of this region of the X chromosome using pulsed-field gel electrophoresis has shown that MN12, St14 and DX13 (DXS15) are physically linked within a region of 470kb. A long range restriction map around the MN12 locus reveals at least two candidate HTF islands, suggesting the existence of expressed sequences in this region.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Chromosome Fragile Sites
  • Chromosome Fragility*
  • Female
  • Humans
  • Male
  • Nucleic Acid Hybridization
  • Nucleotide Mapping
  • Pedigree
  • Plasmids
  • Polymorphism, Genetic*
  • Polymorphism, Restriction Fragment Length*
  • X Chromosome*