Busiello E, Di Girolamo M
Eur J Biochem. 1975 Jun 16;55(1):61-70. doi: 10.1111/j.1432-1033.1975.tb02138.x.
Nuclei with low cytoplasmic contamination, capable of synthesizing RNA for an extended period of time, were prepared from HeLa cells. Besides elongating RNA chains already initiated in vivo, the nuclear preparation initiates the synthesis of new RNA chains. This was shown by labelling the newly synthesized RNA with [gamma-32P]GTP and by detecting the presence of labelled guanosine tetraphosphate among the alkaline hydrolysis products of synthesized RNA. By synthesizing RNA in the presence of each of the four gamma-32P-labelled nucleoside triphosphates, it was possible to conclude that RNA chain synthesis starts predominantly with a purine base. Both nucleolar and nucleoplasmic RNAs are made. The nuclear preparation methylates the nucleolar RNA by utilizing S-adenosyl-L-methionine as a methyl-group donor.
从HeLa细胞中制备出细胞质污染低、能够长时间合成RNA的细胞核。除了延长已在体内起始的RNA链外,该细胞核制剂还能起始新RNA链的合成。这通过用[γ-32P]GTP标记新合成的RNA以及在合成RNA的碱性水解产物中检测标记的鸟苷四磷酸的存在得以证明。通过在四种γ-32P标记的核苷三磷酸各自存在的情况下合成RNA,可以得出RNA链合成主要以嘌呤碱基起始的结论。核仁RNA和核质RNA均有合成。该细胞核制剂利用S-腺苷-L-甲硫氨酸作为甲基供体使核仁RNA甲基化。