Burns D M, Rodi C P, Agris P F
Cancer Biochem Biophys. 1976;1(6):269-80.
N6-(delta2-isopentenyl)adenosine was found both as a component of tRNA and as the cytoplasmic mononucleotide in human leukemic lymphoblasts and myeloblasts from peripheral blood and bone marrow samples. This hypermodified nucleotide was also found in the tRNA and as a mononucleotide in human (MRC-5 and KB) and mouse (A9, FLV, LM, and RAG) cell lines. The relative amounts of this hypermodified nucleotide in the tRNA of the cell lines and the human leukemias were similar (the mean value being 0.06 +/- 0.03 mole % of the total tRNA nucleotide content); whereas the amounts occurring as the free cytoplasmic mononucleotide were more varied but still comparable (the mean value being 0.53 +/- .09 mole % of all cytoplasmic nucleotides) for all cells investigated with the notable exception of all normal, diploid cell lines under study (0.04 mole%). A possible relationship of the free cytoplasmic mononucleotide with the nucleotide in the tRNA for control of mammalian cell protein synthesis in vivo was investigated by addition of N6-(delta2-isopentenyl)adenosine to the culture medium. The exogenously added nucleoside caused inhibition of cell growth within 3 h and cell death within 36 h at concentrations as low as 0.4 muM. No comparable effects were seen when adenosine, adenine, or N6-(delta2-isopentenyl)-adenine were added to the cultures. The simultaneous presence of adenosine in cultures containing N6-(delta2-isopentenyl)adenosine did not alter the detrimental effects of the hypermodified nucleoside on cell growth even when the concentration of adenosine was 50-fold that of N6-(delta2-isopentenyl)adenosine. Addition of N6-(delta2-isopentenyl)adenosine to cell cultures caused within the first 6 h a significant reduction in the rates of RNA and protein synthesis; whereas DNA synthesis continued at a rate comparable to control and adenosine-treated cells for 18 h before decreasing.
在来自外周血和骨髓样本的人类白血病淋巴母细胞和成髓细胞中,N6-(δ2-异戊烯基)腺苷既作为tRNA的组成成分,也作为细胞质单核苷酸被发现。这种高度修饰的核苷酸在人类(MRC-5和KB)和小鼠(A9、FLV、LM和RAG)细胞系的tRNA中以及作为单核苷酸也被发现。该高度修饰核苷酸在细胞系和人类白血病tRNA中的相对含量相似(平均值为总tRNA核苷酸含量的0.06±0.03摩尔%);而作为游离细胞质单核苷酸存在的量变化更大,但对于所有研究的细胞来说仍具有可比性(平均值为所有细胞质核苷酸的0.53±0.09摩尔%),但所研究的所有正常二倍体细胞系除外(0.04摩尔%)。通过向培养基中添加N6-(δ2-异戊烯基)腺苷,研究了游离细胞质单核苷酸与tRNA中的核苷酸在体内控制哺乳动物细胞蛋白质合成方面的可能关系。外源添加的核苷在浓度低至0.4μM时,在3小时内导致细胞生长受到抑制,并在36小时内导致细胞死亡。当向培养物中添加腺苷、腺嘌呤或N6-(δ2-异戊烯基)腺嘌呤时,未观察到类似的效果。在含有N6-(δ2-异戊烯基)腺苷的培养物中同时存在腺苷,即使腺苷的浓度是N6-(δ2-异戊烯基)腺苷的50倍,也不会改变高度修饰核苷对细胞生长的有害影响。向细胞培养物中添加N6-(δ2-异戊烯基)腺苷在最初6小时内导致RNA和蛋白质合成速率显著降低;而DNA合成在18小时内以与对照和腺苷处理细胞相当的速率继续进行,然后才下降。