High-Resolution Molecular Characterization of 15q11-q13 Rearrangements by Array Comparative Genomic Hybridization (Array CGH) with Detection of Gene Dosage

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High-Resolution Molecular Characterization of 15q11-q13 Rearrangements by Array Comparative Genomic Hybridization (Array CGH) with Detection of Gene Dosage Nicholas J. Wang, Dahai Liu, Alexander S. Parokonny, N. Carolyn Schanen The American Journal of Human Genetics Volume 75, Issue 2, Pages 267-281 (August 2004) DOI: 10.1086/422854 Copyright © 2004 The American Society of Human Genetics Terms and Conditions

Figure 1 Gapped contig of the clones spotted on the array covering chromosome 15q11-q14. Black bars signify locations of designated clones on chromosome 15q11-q14, and gray bars/boxes represent sequenced regions not represented on the array. Unblackened boxes indicate gaps in the genomic sequence where no clones have been placed. The relative positions of the known breakpoints are indicated. Array clones derived from non–chromosome 15 autosomes, sex chromosomes, and P1 FISH clones are not shown. The American Journal of Human Genetics 2004 75, 267-281DOI: (10.1086/422854) Copyright © 2004 The American Society of Human Genetics Terms and Conditions

Figure 2 The log2 T/R ratio plots for control samples representing various forms of segmental rearrangements of chromosome 15q11-q14. A, Cytogenetically normal control. B, Patient GM-11385 with PWS and a BP2:BP3A deletion. C, Interstitial duplication event between BP1 and BP3B, leading to trisomy in patient 98-19. D, Interstitial duplication between BP2 and BP3A, leading to trisomy in patient 99-9. E, Supernumerary SMC(15) with a BP3B:BP3B junction in patient 03-71, leading to tetrasomy for the involved regions. F, SMC(15) with an asymmetric BP4:BP5 junction in patient 99-70. G, SMC(15) with a BP5:BP5 junction in patient 99-73. H, SMC(15) resulting in partial hexasomy of chromosome 15q11-q14 in patient 00-29. In the plots, only the clones representing chromosome 15q11-q14 are shown. A ratio >0.3 indicated a gain of DNA copy number for the clone, whereas a ratio <−0.3 indicated a loss of DNA copy number. The vertical lines represent the locations of breakpoints, as determined by our array analysis and by published reports. BP3A is not shown but lies between spots 49 and 50. The American Journal of Human Genetics 2004 75, 267-281DOI: (10.1086/422854) Copyright © 2004 The American Society of Human Genetics Terms and Conditions

Figure 3 Standard curve of log2 T/R ratios. The observed ratios for each copy number are represented by blackened squares (±1 SD), with a corresponding trend line. The gray dashed line represents theoretical values at a given copy number (gray diamonds). The American Journal of Human Genetics 2004 75, 267-281DOI: (10.1086/422854) Copyright © 2004 The American Society of Human Genetics Terms and Conditions

Figure 4 Mapping of BP5 by metaphase FISH of patient 03-28. Chromosome 15 homologs are marked by an arrowhead, and the SMC(15) is marked by an arrow. Enlargements of the images are inset, with the top row showing dual color hybridization and the bottom-row red signal arising from the BAC clone. A, Red signals represent clone AC124094 (spot 73), and green signals represent pcm15 (chromosome 15 centromere). Hybridization of AC124094 is seen on the normal homologs and on the SMC(15), with a weaker signal on the SMC(15). B, Red signals represent AC074201 (spot 74), and the green signals represent pcm15. Clone AC074201 hybridizes to the normal chromosome 15 homologs but not to the SMC(15). These data place the breakpoint within clone AC124094, which is consistent with its intermediate fluorescence signal on the array. The American Journal of Human Genetics 2004 75, 267-281DOI: (10.1086/422854) Copyright © 2004 The American Society of Human Genetics Terms and Conditions

Figure 5 Characterization of deletions in patients 00-3 and 99-36 by FISH. Array data charts for 00-3 (A) and 99-36 (B) show a relative decrease in signal intensity for clones in the interval between BP1 and BP2. C, FISH analysis of the BP1–BP2 interval, with clone AC011767 (spot 5, red) and with pcm15 (green). The absence of hybridization of clone AC011767 to one chromosome 15 homolog in metaphase spreads from patient 00-3 was consistently detected, although two paired signals were present on the SMC(15). D, FISH with clone AC138649 (spot 6, red) and with pcm15 (green) on metaphase chromosomes from patient 00-3. Signals for the more telomeric clone, AC138649, were present on both chromosome 15 homologs. E, FISH with clone AC138649 (spot 6, red) and with pcm15 (green) on metaphase chromosomes from patient 99-36. The presence of a single paired signal on the SMC(15) for clone AC138649 indicates that there is only one copy of the region. F, FISH with a more distal clone, AC138687 (spot 8, red), and with pcm15 (green) generating a double signal from clone AC138687, consistent with two copies on the idic(15). C–F, Arrowheads indicate chromosome 15 homologs; arrows indicate the SMC(15). Enlargements of the images are inset, with the top row showing dual color hybridization and the bottom-row red signal arising from the BAC clone. The American Journal of Human Genetics 2004 75, 267-281DOI: (10.1086/422854) Copyright © 2004 The American Society of Human Genetics Terms and Conditions

Figure A1 The log2 T/R ratio array data for patients studied. A, The average log2 T/R ratios for the combined data from five control experiments. Error bars represent ±1 SD. B, The log2 T/R ratios for four patients with interstitial duplications involving a BP1:BP3B recombination event. C and D, Plots of the log2 T/R ratio for the 13 patients carrying an SMC(15) that arose from a symmetrical BP3:BP3 recombination event leading to tetrasomy for the duplicated region. The data were split onto two graphs to facilitate discrimination of the curves. E and F, Data from the remaining 16 patients that carried an asymmetrical SMC(15) that resulted from a BP4:BP5 recombination event leading to tetrasomy proximal to BP4 and trisomy between BP4 and BP5. Again, the data were split arbitrarily onto two graphs to allow better discrimination of the individual lines. The American Journal of Human Genetics 2004 75, 267-281DOI: (10.1086/422854) Copyright © 2004 The American Society of Human Genetics Terms and Conditions