Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28

Am J Med Genet. 1991 Feb-Mar;38(2-3):332-5. doi: 10.1002/ajmg.1320380233.

Abstract

A new polymorphic DNA marker RN1, defining locus DXS369, was recently isolated. Using different somatic cell hybrids, RN1 was mapped between markers 4D-8 and U6.2. We have narrowed the localization of RN1 to the region between 4D-8 and FRAXA by genetic mapping in fragile X [fra(X)] families. Combined with information from other reports, the following order of loci on Xq27-q28 is suggested: cen-F9-(DXS105-DXS152)-DXS98-DXS369-FRAXA- DXS304-(DXS52-DXS15-F8)-tel. The locus DXS369 is closely linked to FRAXA, with a peak lodscore of 18.5 at a recombination fraction of 0.05. Therefore, RN1 is a useful probe for carrier detection and prenatal diagnosis in fra(X) families.

MeSH terms

  • Animals
  • Chromosome Mapping
  • DNA Probes / genetics*
  • Fragile X Syndrome / diagnosis
  • Fragile X Syndrome / genetics*
  • Genetic Carrier Screening
  • Humans
  • Hybrid Cells
  • Pedigree
  • Polymorphism, Restriction Fragment Length*
  • Prenatal Diagnosis
  • X Chromosome*

Substances

  • DNA Probes