Lavignon M, Bertrand J R, Porumb H, Rayner B, Imbach J L, Paoletti C, Malvy C
UA 147 CNRS, U 140 INSERM, Institut G. Roussy, Villejuif, France.
Nucleic Acids Symp Ser. 1991(24):117-9.
RNA is not cleaved as a consequence of the binding of RNase H to the duplex between RNA and a complementary alpha-oligodeoxyribonucleotide (oligo). In consequence targets have been selected which do not a priori require the action of RNase H to inhibit genetic expression. Two models have been used: The Friend Murine Leukemia Virus (F-MuLV) and the synthesis of rabbit beta globin.alpha-oligos trigger specific inhibitions in both systems. The functionalisation in 5' with the intercalating agent 9-NH2-ellipticine renders the oligos resistant to degradation and allows a direct action on cells.
RNA不会因核糖核酸酶H(RNase H)与RNA和互补α-寡脱氧核糖核苷酸(oligo)之间的双链体结合而被切割。因此,已选择了一些靶点,这些靶点在抑制基因表达时并非先验地需要RNase H的作用。使用了两种模型:Friend小鼠白血病病毒(F-MuLV)和兔β珠蛋白的合成。α-寡核苷酸在这两个系统中均引发特异性抑制。用嵌入剂9-氨基椭圆玫瑰树碱在5'端进行功能化修饰,可使寡核苷酸抗降解,并能直接作用于细胞。