A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndrome
Articolo
Data di Pubblicazione:
1986
Citazione:
A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndrome / S. Russo, M. Mencarelli, F. Cavalleri, A. Selicorni, F. Cogliati, L. Larizza. - In: MOLECULAR AND CELLULAR PROBES. - ISSN 0890-8508. - 17:6(1986), pp. 295-299.
Abstract:
The quantitative evaluation of mosaicism for uniparental disomy (UPD) involving a restricted chromosomal region requires the availability of a sensitive and reproducible method that is capable of detecting even a small percentage of disomic cells and avoiding false positive and false negative results. The occurrence of UPD is usually monitored by means of the parent-proband segregation analysis of microsatellites mapping to the target region. We here describe the quantitative blood cell evaluation of segmental mosaic UPD11, a marker of Beckwith-Wiedemann syndrome, by means of the segregation analysis of 11p15 microsatellites using both radioactive and fluorescence-based techniques. As the greater amplification efficiency of the shorter allele in heterozygous subjects may bias the correct evaluation of disomy, the mean short/long allele ratio was established at three loci of each of 30 normal heterozygous subjects, as well as the peak As/Al area in the presence of 50% of each allele. The interval was defined using a 5% level of significance. The results show that the fluorescence-based technique is superior to radioactivity in detecting the subtle allelic imbalances present in low-grade mosaicism conditions.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
Uniparental Disomy ; Microsatellite Repeats ; Alleles ; Mosaicism ; Humans ; Fluorescent Dyes ; Isotope Labeling ; Beckwith-Wiedemann Syndrome ; Genomic Imprinting ; Chromosomes, Human, Pair 11
Elenco autori:
S. Russo, M. Mencarelli, F. Cavalleri, A. Selicorni, F. Cogliati, L. Larizza
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