Cooper D L, Marzluff W F
J Biol Chem. 1978 Dec 10;253(23):8375-80.
Isolated nuclei frommouse myeloma cells which were active in RNA synthesis did not synthesize detectable amounts of poly(A)-containing RNA. On addition of a soluble protein extract from crude nuclei, the highly purified nuclei synthesized significanamounts of poly(A)-containing RNA, as analyzed by chromatography on poly(U)-Sepharose. The poly(A) tract was totally synthesized de novo and was indistinguishable from poly(A) synthesized in vivo. Twenty per cent of the RNA polymerase II products were polyadenylated. More than 80% of the newly synthesized poly(A) was present on molecules at least partially transcribed in vitro. The transcription and polyadenylation reaction could be separated temporally and a portion (10%) of the polyadenylated RNA was released into the extra nuclear fraction. We conclude that this system carries out one RNA processing reaction, polyadenylation, faithfully.
从小鼠骨髓瘤细胞中分离出的、在RNA合成中具有活性的细胞核,不能合成可检测量的含多聚腺苷酸(poly(A))的RNA。加入来自粗核的可溶性蛋白质提取物后,经聚尿苷酸 - 琼脂糖层析分析,高度纯化的细胞核合成了大量含poly(A)的RNA。poly(A)序列完全是重新合成的,与体内合成的poly(A)无法区分。RNA聚合酶II产物的20%进行了多聚腺苷酸化。新合成的poly(A)中超过80%存在于至少部分在体外转录的分子上。转录和多聚腺苷酸化反应在时间上可以分开,并且一部分(10%)多聚腺苷酸化的RNA被释放到核外部分。我们得出结论,该系统忠实地进行了一种RNA加工反应,即多聚腺苷酸化。