Goldenberg C J, Raskas H J
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5430-4. doi: 10.1073/pnas.78.9.5430.
Early region 2 of the adenovirus 2 genome (map position 61-75) specifies two poly(A)+ nuclear RNAs (28S and 23S) that appear to be precursors of the 20S cytoplasmic mRNA [Goldenberg, C. J. & Raskas, H. J. (1979) Cell 16, 131-138]. Splicing of these nuclear RNAs in vitro has been obtained with a whole cell extract prepared from MOPC-315 mouse myeloma cells. The in vitro reaction excises sequences from two introns and attaches 5' sequences to the mRNA body. The splicing reaction was demonstrated by two procedures: (i) hybridization of pulse-labeled RNA fractionated by size and (ii) annealing of RNAs with radioactive DNA probes followed by nuclease digestion. The first procedure provided evidence that sequences from the large 2300-nucleotide intron (74.6-68.8) were excised and 5' transcripts were spliced to the mRNA body. Utilizing both S1 and Exo VII nucleases, the second procedure demonstrated excision of sequences from the smaller 720-nucleotide intron (68.5-66.3), the splicing of sequences from the second leader (68.8) to the mRNA body, and the formation of an mRNA body of 1700 nucleotides, the size found in vivo. These findings provide evidence that an in vitro system that splices viral RNAs to yield products comparable to those found in vivo is now available.
腺病毒2基因组的早期区域2(图谱位置61 - 75)可编码两种聚腺苷酸化核RNA(28S和23S),它们似乎是20S细胞质mRNA的前体[戈尔登伯格,C. J. & 拉斯卡斯,H. J.(1979年)《细胞》16卷,第131 - 138页]。用从MOPC - 315小鼠骨髓瘤细胞制备的全细胞提取物已实现了这些核RNA的体外剪接。体外反应从两个内含子中切除序列,并将5'端序列连接到mRNA主体上。通过两种方法证实了剪接反应:(i)对按大小分级的脉冲标记RNA进行杂交,以及(ii)将RNA与放射性DNA探针退火,随后进行核酸酶消化。第一种方法提供了证据,证明来自2300个核苷酸的大内含子(74.6 - 68.8)的序列被切除,5'端转录本被剪接到mRNA主体上。利用S1核酸酶和外切核酸酶VII,第二种方法证明了来自较小的720个核苷酸内含子(68.5 - 66.3)序列的切除、第二个前导序列(68.8)的序列与mRNA主体的剪接,以及形成了1700个核苷酸的mRNA主体,这是在体内发现的大小。这些发现提供了证据,表明现在已有一种体外系统,可将病毒RNA剪接以产生与体内发现的产物相当的产物。