McGuire P M, Swart C, Hodge L D
Proc Natl Acad Sci U S A. 1972 Jun;69(6):1578-82. doi: 10.1073/pnas.69.6.1578.
The nuclear synthesis of adenovirus-specific RNA late in the infectious cycle in the presence of toyocamycin (an adenosine analogue) has been investigated. There is reduced synthesis of viral RNA with an accumulation of virus-specific RNA in the molecular weight range of at least 4 to 8 x 10(6). No new viral RNA associates with cytoplasmic polyribosomes. In addition, hybridization competition experiments indicate a 70% competition between these large nuclear transcripts and polyribosome-associated viral RNA that was synthesized in the absence of inhibitor. These data are consistent with the following interpretations: complete nuclear processing of viral RNA is necessary for polyribosome association, and precursor viral message(s) contain sequences that are lost normally during post-transcriptional processing.
已对在感染周期后期,在存在丰加霉素(一种腺苷类似物)的情况下腺病毒特异性RNA的核合成进行了研究。病毒RNA的合成减少,在至少4至8×10⁶分子量范围内积累了病毒特异性RNA。没有新的病毒RNA与细胞质多聚核糖体结合。此外,杂交竞争实验表明,这些大的核转录本与在无抑制剂情况下合成的多聚核糖体相关病毒RNA之间存在70%的竞争。这些数据与以下解释一致:病毒RNA的完全核加工对于多聚核糖体结合是必要的,并且前体病毒信息包含在转录后加工过程中通常会丢失的序列。