Knoll J H, Cheng S D, Lalande M
Division of Genetics, Children's Hospital/Harvard Medical School, Boston, Massachusetts 02115.
Nat Genet. 1994 Jan;6(1):41-6. doi: 10.1038/ng0194-41.
DNA replication within chromosome 15q11-q13, a region subject to genomic imprinting, was examined by fluorescence in situ hybridization. Asynchronous replication between homologues was observed in cells from normal individuals and in Prader-Willi (PWS) and Angelman syndrome (AS) patients with chromosome 15 deletions but not in PWS patients with maternal uniparental disomy. Opposite patterns of allele-specific replication timing between homologous loci were observed; paternal early/maternal late at D15S63, D15S10 and the gamma-aminobutyric acid receptor beta 3 subunit gene (GABRB3); and maternal early/paternal late at the more distal gamma-aminobutyric acid receptor alpha 5 subunit gene (GABRA5). At the most distal locus examined, D15S12, both patterns of allele-specific replication timing were detected.
利用荧光原位杂交技术检测了15q11 - q13染色体区域(该区域存在基因组印记)内的DNA复制情况。在正常个体以及患有15号染色体缺失的普拉德 - 威利综合征(PWS)和天使综合征(AS)患者的细胞中观察到同源染色体之间的异步复制,但在母源单亲二体的PWS患者中未观察到。在同源基因座之间观察到等位基因特异性复制时间的相反模式;在D15S63、D15S10和γ-氨基丁酸受体β3亚基基因(GABRB3)处,父本早/母本晚;在更远端的γ-氨基丁酸受体α5亚基基因(GABRA5)处,母本早/父本晚。在所检测的最远端基因座D15S12处,检测到了两种等位基因特异性复制时间模式。