Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS): implications for mapping and cloning the BOR gene

Genomics. 1996 Jan 15;31(2):201-6. doi: 10.1006/geno.1996.0032.

Abstract

Genetic linkage analysis has previously mapped the locus for the autosomal dominant disorder branchio-oto-renal syndrome (BOR) to the pericentric region of chromosome 8q. A YAC contig spanning the putative BOR region, from D8S543 to D8S541, was constructed and confirmed by sequence-tagged site content mapping using microsatellite markers and by DNA hybridization analysis. YACs spanning the BOR interval were used as fluorescence in situ hybridization probes on a cell line from a patient with BO and tricho-rhino-phalangeal syndrome I that involves a chromosome 8q rearrangement. In addition to the cytogenetically defined direct insertion of material from 8q13.3-q21.13 into 8q24.11, a previously unidentified deletion of just under one megabase was found in 8q13.3. These data narrowed the most likely location of the BOR gene to a region corresponding to the proximal two-thirds of YAC 869E10 between D8S543 and D8S279.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Base Sequence
  • Branchial Region / abnormalities*
  • Chromosome Mapping
  • Chromosomes, Artificial, Yeast / genetics
  • Cloning, Molecular
  • DNA Primers
  • Hearing Disorders / genetics*
  • Humans
  • Kidney / abnormalities*
  • Langer-Giedion Syndrome / genetics*
  • Molecular Sequence Data
  • Sequence Deletion

Substances

  • DNA Primers