Wiegant J, Ried T, Nederlof P M, van der Ploeg M, Tanke H J, Raap A K
Department of Cytochemistry and Cytometry, Leiden, The Netherlands.
Nucleic Acids Res. 1991 Jun 25;19(12):3237-41. doi: 10.1093/nar/19.12.3237.
We have used fluorescein-11-dUTP in a nick-translation format to produce fluoresceinated human nucleic acid probes. After in situ hybridization of fluoresceinated DNAs to human metaphase chromosomes, the detection sensitivity was found to be 50-100 kb. The feasibility and the increase in detection sensitivity of microscopic imaging of in situ hybridized, fluoresceinated DNA with an integrating solid state camera for rapid cosmid mapping is illustrated. Combination of fluoresceinated DNA with biotinated and digoxigeninated DNAs allowed easy performance of triple fluorescence in situ hybridization. The potential of these techniques for DNA mapping, cytogenetics and biological dosimetry is briefly discussed.
我们已采用缺口平移法使用荧光素-11-dUTP来制备荧光标记的人核酸探针。将荧光标记的DNA与人类中期染色体进行原位杂交后,检测灵敏度可达50 - 100 kb。文中展示了利用积分固态相机对原位杂交的荧光标记DNA进行显微成像以实现快速黏粒作图的可行性及检测灵敏度的提高。荧光标记的DNA与生物素化和地高辛素化的DNA相结合,使得三重荧光原位杂交易于进行。简要讨论了这些技术在DNA作图、细胞遗传学和生物剂量测定方面的潜力。