Construction of a physical and transcript map for a 1-Mb genomic region containing the urofacial (Ochoa) syndrome gene on 10q23-q24 and localization of the disease gene within two overlapping BAC clones (<360 kb)

Genomics. 1999 Aug 15;60(1):12-9. doi: 10.1006/geno.1999.5908.

Abstract

Urofacial (Ochoa) syndrome is an autosomal recessive disease characterized by distorted facial expression and urinary abnormalities. Previously, we mapped the UFS gene to chromosome 10q23-q24 and narrowed the interval to one YAC clone of 1410 kb. Here, we have constructed a BAC/PAC contig of the 1-Mb region using STS content mapping with 42 BAC/PAC-end sequences, 9 previously reported and 16 newly identified microsatellite markers, and 14 EST markers. A total of 26 polymorphic microsatellite markers were genotyped for 31 UFS patients from Colombia and 2 patients from the United States. Haplotype analyses suggest that the UFS gene is located within two overlapping BAC clones, a region of <360 kb of DNA sequence. We tested 42 EST markers previously mapped to the D10S1709-D10S603 interval against the BAC/PAC contig and identified 11 ESTs located in the 1-Mb region. Four of the 11 ESTs mapped to the 360-kb UFS critical region. Shotgun sequencing of the two BAC clones and BLASTN search of the EST databases revealed 3 other ESTs contained in the UFS critical region. These results will facilitate the cloning and identification of the UFS gene.

Publication types

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

MeSH terms

  • Bacteriophage P1 / genetics
  • Chromosomes, Bacterial / genetics
  • Chromosomes, Human, Pair 10 / genetics*
  • Cloning, Molecular
  • Contig Mapping
  • DNA / genetics*
  • Facial Expression*
  • Family Health
  • Female
  • Genetic Markers
  • Haplotypes
  • Humans
  • Male
  • Pedigree
  • Physical Chromosome Mapping
  • Polymorphism, Genetic
  • Syndrome
  • Urinary Bladder, Neurogenic / genetics*

Substances

  • Genetic Markers
  • DNA