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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)

  • Cong Yi Wang
    ,
  • Jing Da Shi
    ,
  • Yi Qun Huang
    ,
  • Pedro E. Cruz
    ,
  • Bernardo Ochoa
    ,
  • Bobbilynn Hawkins-Lee
*Corresponding author for this work
  • University of Florida
    ,
  • Universidad de Antioquia
Scholary Output:
Contribution to journal
Article
Peer-review

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 E ST databases revealed 3 other ESTs contained in the UFS critical region. These results will facilitate the cloning and identification of the UFS gene.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 12-19 (8 pages)

Journal (Volume, Issue Number)

Genomics (Volume 60, Issue 1)

Publication milestones

  • Published - 08/15/1999

Publication status

Published - 08/15/1999

ISSN

0888-7543

Publication IDs

  • Scopus: 0344995248
  • PubMed: 10458906

Publication metrics

Metrics

SciVal
FWCI
0.25
SciVal
Author count
8
SciVal
citations
18
SciVal
Paper percentile
67
Fractional count
2
Fractional count
0.25
Fractional count
6
Fractional count
0.75
Fractional count
2
Fractional count
1
Scopus
citations

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Citation count
18
Mentions
1
Captures
19

Funding Details

This study was supported by a grant (1R01DK53266) from the National Institutes of Health. The authors thank all participating families for donating blood samples for this project. Special thanks are due to Dr. Richard A. Spritz for kindly supplying the P1 clone and to Dr. R. K. Wilson for providing expert suggestions on random sequencing.
FundersFunding number
NIH
-
NIDDK
R01DK053266