Kolodny G M
Nucleic Acids Res. 1977 Feb;4(2):271-84. doi: 10.1093/nar/4.2.271.
3H uridine and 3H guanosine labeled oligonucleotides were separately produced by degradation of high molecular weight RNA by endogenous intracellular ribonucleases of HeLa cells. After incubation of this low molecular weight RNA with HeLa cells under conditions limiting labeled mononucleotide incorporation, significant label was found in high molecular weight 18s RNA, but not in 28s RNA. The label in the 18s RNA was alkali labile and remained with the 18s RNA peak under denaturation conditions. Actinomycin in the incubation mixture prevented the appearance of label in the 18s RNA. These results raise the possibility that exogenous oligonucleotide segments can be incorporated en bloc into RNA.
3H尿苷和3H鸟苷标记的寡核苷酸分别通过HeLa细胞内源性细胞核糖核酸酶降解高分子量RNA产生。在限制标记单核苷酸掺入的条件下,将这种低分子量RNA与HeLa细胞一起孵育后,在高分子量18s RNA中发现了显著的标记,但在28s RNA中未发现。18s RNA中的标记对碱不稳定,并且在变性条件下仍与18s RNA峰一起存在。孵育混合物中的放线菌素可防止18s RNA中出现标记。这些结果增加了外源性寡核苷酸片段可以整体掺入RNA的可能性。