We have isolated a DNA segment absent from all the constitutionally deleted chromosomes 11 of our patients with Wilms tumor. This marker separates two balanced translocations that break in band 11p13: the distal one associated with aniridia (AN2), and the proximal one with genitourinary dysplasia (GUD). The GUD breakpoint maps within the smallest region of overlap (SRO) for the Wilms tumor (WT) gene locus, thus strengthening the previous suggestion of an association between Wilms tumor and other abnormalities of the genitourinary system. The 11p13 translocation breakpoint associated with T-cell acute lymphatic leukemia (T-ALL) is centromeric to the SRO and separated from the WT locus by at least one known gene. This region of the human genome (11p13) is rich in CpG islands that potentially identify genes, some of which may be involved in the various phenotypes associated with the WAGR syndrome. This is consistent with the proposition that the majority of human genes are in G-negative bands.
|Number of pages||9|
|Publication status||Published - 1989|
- Animals Aniridia/*genetics Blotting, Southern Chromosome Mapping *Chromosomes, Human, Pair 11 DNA/*isolation & purification Dinucleoside Phosphates/analysis Genes Humans Hybrid Cells Kidney Neoplasms/*genetics Mice Restriction Mapping Syndrome *Translocation, Genetic *Urogenital Abnormalities Wilms Tumor/*genetics