Landegent J E, Jasen in de Wal N, Baan R A, Hoeijmakers J H, Van der Ploeg M
Exp Cell Res. 1984 Jul;153(1):61-72. doi: 10.1016/0014-4827(84)90448-8.
A new approach is presented for the indirect hybridocytochemical localization of specific nucleic acid sequences in microscopic preparations. The method is based on the application of probes modified with N-acetoxy-2-acetylaminofluorene. After hybridization, the 2-acetylaminofluorene-labelled probes are recognized by antibodies directed against modified guanosine and visualized immunocytochemically. This procedure has been optimized on two model objects: mouse satellite DNA in interphase nuclei and chromosomes, and kinetoplast DNA in Crithidia fasciculata. A first application that may be of clinical importance is given by the detection of human cytomegalovirus in infected human lung fibroblasts. Other potentials of this procedure are discussed. Its advantages are: (1) the simple, rapid and reproducible labelling procedure; (2) the high stability of both label and modified probes; (3) the feasibility of labelling both double-stranded (ds) and single-stranded (ss) probes (DNA as well as RNA); (4) the rapid and sensitive detection of hybrids.
本文介绍了一种在显微镜标本中对特定核酸序列进行间接杂交细胞化学定位的新方法。该方法基于应用用N-乙酰氧基-2-乙酰氨基芴修饰的探针。杂交后,针对修饰鸟苷的抗体可识别2-乙酰氨基芴标记的探针,并通过免疫细胞化学进行可视化。此程序已在两个模型对象上进行了优化:间期细胞核和染色体中的小鼠卫星DNA,以及克氏锥虫中的动质体DNA。该方法在临床上可能具有重要意义的首个应用是检测感染人肺成纤维细胞中的人巨细胞病毒。文中还讨论了该程序的其他潜力。其优点包括:(1)标记程序简单、快速且可重复;(2)标记物和修饰探针的稳定性高;(3)标记双链(ds)和单链(ss)探针(DNA以及RNA)的可行性;(4)对杂交体的快速灵敏检测。