Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader‐Willi syndrome

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Abstract
Ten genomic DNA probes, subcloned from inserts derived from a phage library constructed from the DNA of flow‐sorted chromosomes, have now been mapped to locations within 15q11–15q13. By dosage blotting and densitometry, 5 of these probes map to the 15q11.2–15q12 segment missing in one 15 chromosome of a Prader‐Willi syndrome (PWS) patient with a prominent cytological deletion. A sixth probe most likely maps to the same region. The other 4 probes map outside of this segment but within 15q11–15q13. Several of the 15q11.2–15q12 probes, and a cDNA probe homologous to one, have been used to test the DNA from 8 patients exhibiting a wide range of the clinical manifestations expected for PWS patients. DNA deletion was observed in all 3 patients with cytological 15q1 deletions as well as in a patient with an unbalanced (Y;15) translocation. DNA from 1 PWS patient with an unbalanced (5; 15) translocation and an inverted duplication of the short arm and proximal long arm of 15 showed at least 1 and possibly 2 extra copies of each genomic probe tested. In the other 3 patients with no cytological deletions, no DNA deletions were found. Thus, the molecular probes described can be used in most PWS patients to analyze the region of proximal 15q implicated in this syndrome.