Hopman A H, Wiegant J, Raap A K, Landegent J E, van der Ploeg M, van Duijn P
Histochemistry. 1986;85(1):1-4. doi: 10.1007/BF00508646.
A non-radioactive in situ hybridization technique is described which allows the simultaneous detection of different DNA sequences. To demonstrate the feasibility of the procedure, metaphases and interphase nuclei of a human-mouse somatic cell hybrid were simultaneously hybridized with mercurated total human DNA and a biotinylated mouse satellite DNA probe. After the hybridization, the probes were detected immunocytochemically using two different and independent affinity systems. By this approach we visualized the two DNA target sequences in metaphase chromosomes and in interphase nuclei with FITC and TRITC fluorescence, or blue (alkaline phosphatase) and brown (peroxidase) precipitated enzyme products. This method not only allows detection of intact chromosomes but also the visualization of rearrangements between parts of human and mouse chromosomes. Furthermore, the technique demonstrates the high topological resolution of non-radioactive in situ hybridizations.
本文描述了一种非放射性原位杂交技术,该技术可同时检测不同的DNA序列。为证明该方法的可行性,将人-鼠体细胞杂种的中期染色体和间期核同时与汞化的总人DNA和生物素化的小鼠卫星DNA探针杂交。杂交后,使用两种不同且独立的亲和系统通过免疫细胞化学方法检测探针。通过这种方法,我们用异硫氰酸荧光素(FITC)和四甲基异硫氰酸罗丹明(TRITC)荧光,或蓝色(碱性磷酸酶)和棕色(过氧化物酶)沉淀的酶产物在中期染色体和间期核中观察到了两种DNA靶序列。该方法不仅能够检测完整的染色体,还能观察到人染色体和小鼠染色体部分之间的重排。此外,该技术证明了非放射性原位杂交具有高拓扑分辨率。