Journal of Pediatric Urology
Volume 2, Issue 4 , Pages 233-242, August 2006

Deletion mapping of critical region for hypospadias, penoscrotal transposition and imperforate anus on human chromosome 13

  • Nilda M. Garcia

      Affiliations

    • Department of Surgery, University of Texas Southwestern Medical Center, Dallas, TX, USA
  • ,
  • Jocelyn Allgood

      Affiliations

    • Departments of Urology, University of Texas Southwestern Medical Center, 5325 Harry Hines Boulevard, U9110, Dallas, TX 75390-9110, USA
  • ,
  • Lane J. Santos

      Affiliations

    • McDermott Center for Human Growth & Development, University of Texas Southwestern Medical Center, Dallas, TX, USA
  • ,
  • Devin Lonergan

      Affiliations

    • Departments of Urology, University of Texas Southwestern Medical Center, 5325 Harry Hines Boulevard, U9110, Dallas, TX 75390-9110, USA
  • ,
  • J.R. Batanian

      Affiliations

    • Department of Pediatrics, Pediatrics Research Institute, University of Saint-Louis, MO, USA
  • ,
  • Christopher Dravis

      Affiliations

    • Center for Developmental Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA
  • ,
  • Mark Henkemeyer

      Affiliations

    • Center for Developmental Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA
  • ,
  • Oliver Bartsch

      Affiliations

    • Institut für Klinische Genetik, Universitätsklinikum, Technische Universität, University Hospital Carl Gustav Carus, Dresden, Germany
  • ,
  • Roger A. Schultz

      Affiliations

    • Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA
  • ,
  • Andrew R. Zinn

      Affiliations

    • McDermott Center for Human Growth & Development, University of Texas Southwestern Medical Center, Dallas, TX, USA
  • ,
  • Linda A. Baker

      Affiliations

    • Departments of Urology, University of Texas Southwestern Medical Center, 5325 Harry Hines Boulevard, U9110, Dallas, TX 75390-9110, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1 214 648 2278; fax: +1 214 648 8786.

Received 18 October 2005; accepted 7 March 2006. published online 11 July 2006.

Abstract 

Background

The 13q-deletion syndrome causes human congenital birth defects due to the loss of regions of one long arm of human chromosome 13. A distal critical region for severe genitourinary and anorectal birth defects in the region of 13q32.2–34 has been suggested; we sought to narrow this critical region.

Methods

From patients with karyotypes revealing haploinsufficiency for distal chromosome 13q and their parents, peripheral blood was obtained and lymphocytes were immortalized for DNA isolation. Genetic and molecular cytogenetic methods were used to map deletions. Patient and parental samples were genotyped with a panel of 20 microsatellite markers spanning 13q31.3–qter and deletions identified by loss of heterozygosity. Deletions were also mapped using a panel of 35 BAC clones from the same region as probes for fluorescence in situ hybridization on patient lymphoblastoid metaphase preparations. The data were synthesized and a deletion map defining the critical region was generated.

Results

Eight patients with known deletions around 13q32–qter and their parents were analyzed, and categorized into three groups: three patients without anorectal or genitourinary anomalies (hypospadias, penoscrotal transposition), four male patients with anorectal and/or genitourinary anomalies, and one XY patient with ambiguous genitalia without anorectal anomalies. We mapped the critical region for anorectal and genitourinary anomalies to an ∼9.5-Mb interval of 13q33.3–q34 delineated by markers D13S280–D13S285; this spans ∼8% of the chromosome and contains 20 annotated genes.

Conclusion

The critical region of chromosome 13q mediating genitourinary/anorectal anomalies has been further narrowed to a ∼9.5 Mb region on 13q33.3–q34. Identification of the gene(s) mediating these syndromic genitourinary defects should further our knowledge on molecular mediators of non-syndromic hypospadias, penoscrotal transposition and anorectal malformations.

Keywords: Chromosome, 13q, Hypospadias, Penoscrotal Transposition, Anorectal malformation, Deletion, Haploinsufficiency

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PII: S1477-5131(06)00059-3

doi:10.1016/j.jpurol.2006.03.006

Journal of Pediatric Urology
Volume 2, Issue 4 , Pages 233-242, August 2006