Weber J, Blanchard J M, Ginsberg H, Darnell J E
J Virol. 1980 Jan;33(1):286-91. doi: 10.1128/JVI.33.1.286-291.1980.
A study of the processing of mRNA from two early adenovirus type 2 transcription units (regions 2 and 4 of adenovirus type 2 genome; [J. Flint, Cell 10:153--166, 1977]) revealed that polyadenylic acid [poly(A)] was added in most if not all cases to an unspliced nuclear RNA molecule whose coordinates extended from the apparent initiation site for RNA synthesis to the single poly(A) site in each transcription unit. An intermediate RNA molecule in the processing of the mRNA for the 72,000-M, single-stranded DNA binding protein showed that the first of the two intervening sequences, the one closest to the 5' end of the molecule, was removed first at least in the majority of the processed molecules. Finally, in cells labeled for 10 min and then treated with actinomycin D to stop further RNA synthesis, the majority, if not all, of the poly(A)-terminated nuclear RNA specific for region 2 was successfully processed and transported to the cytoplasm.
一项关于来自两个早期腺病毒2型转录单位(腺病毒2型基因组的2区和4区;[J. 弗林特,《细胞》10:153 - 166,1977])的mRNA加工过程的研究表明,在大多数(即便不是所有)情况下,聚腺苷酸[poly(A)]会添加到一个未剪接的核RNA分子上,该分子的坐标从RNA合成的明显起始位点延伸至每个转录单位中的单个poly(A)位点。在加工72,000-M的单链DNA结合蛋白的mRNA过程中的一个中间RNA分子表明,两个间隔序列中的第一个,即最靠近分子5'端的那个,至少在大多数加工后的分子中是首先被去除的。最后,在用放线菌素D处理以停止进一步RNA合成之前标记10分钟的细胞中,大多数(即便不是所有)特定于2区的poly(A)末端核RNA都成功地进行了加工并转运到了细胞质中。