Thornhill A R, Monk M
Molecular Embryology Unit, Institute of Child Health, London, UK.
Mol Hum Reprod. 1996 Apr;2(4):285-9. doi: 10.1093/molehr/2.4.285.
We recently described a new procedure, called 'cell recycling', which combines the two powerful techniques of polymerase chain reaction (PCR) and fluorescent in-situ hybridization (FISH) on the same single fixed cell. The dual procedure was developed to single cell sensitivity using single blastomeres of preimplantation mouse embryos. We have now extended the procedure to single human cells and demonstrated its potential use in preimplantation diagnosis to detect Duchenne muscular dystrophy (DMD) by PCR, in addition to sexing the same single cell by both PCR and FISH. Here we report an efficiency of 65% for cell recycling with efficiencies for PCR ampification of a single copy DMD sequence at 87% and sexing by FISH at 75%. Should PCR diagnosis of the DMD mutation fail, cell recycling would provide two opportunities to identify the sex of the embryo, allowing selection of only the female embryos for transfer.
我们最近描述了一种名为“细胞回收”的新方法,该方法将聚合酶链反应(PCR)和荧光原位杂交(FISH)这两种强大的技术结合在同一个固定的单细胞上。这种双重方法是利用植入前小鼠胚胎的单个卵裂球开发的,以达到单细胞灵敏度。我们现在已将该方法扩展到单个人类细胞,并证明了其在植入前诊断中的潜在用途,即通过PCR检测杜氏肌营养不良症(DMD),此外还可通过PCR和FISH对同一个单细胞进行性别鉴定。在此我们报告细胞回收的效率为65%,其中单拷贝DMD序列的PCR扩增效率为87%,FISH性别鉴定效率为75%。如果DMD突变的PCR诊断失败,细胞回收将提供两次鉴定胚胎性别的机会,从而仅选择雌性胚胎进行移植。