Ernoult-Lange M, May E
J Virol. 1983 Jun;46(3):756-67. doi: 10.1128/JVI.46.3.756-767.1983.
By means of S1 mapping, we observed that spliced 16S and 19S viral late mRNAs--in addition to early mRNAs--were present in cytoplasmic polyadenylated RNA preparations from simian virus 40-transformed cell lines of rat or mouse origin containing no detectable amount of free viral DNA. The amounts of early and late virus-specific mRNAs in these lines were quantified by hybridization of radioactive cytoplasmic polyadenylated RNA with cloned region-specific restriction fragments. The relative amount of late viral mRNA produced in these transformed cells was found to be of the same order as that produced in simian virus 40-infected, nonpermissive baby mouse kidney cells. Moreover, by using the S1 nuclease protection method, we compared the 5' ends of late mRNAs produced (i) in transformed cells, (ii) in abortively infected mouse cells, and (iii) in the late phase of the lytic cycle. The 5' ends of late mRNAs both in abortively infected and in transformed cells were less heterogeneous than the 5' ends of late mRNAs produced during the lytic cycle; however, they were a subset of the 5' ends of late transcripts produced in the lytic cycle.
通过S1图谱分析,我们观察到,除了早期mRNA外,在来自大鼠或小鼠来源的猿猴病毒40转化细胞系的细胞质多聚腺苷酸化RNA制剂中,存在剪接的16S和19S病毒晚期mRNA,这些细胞系中未检测到游离病毒DNA。通过用放射性细胞质多聚腺苷酸化RNA与克隆的区域特异性限制性片段杂交,对这些细胞系中早期和晚期病毒特异性mRNA的量进行了定量。发现这些转化细胞中产生的晚期病毒mRNA的相对量与在猿猴病毒40感染的、非允许性的幼鼠肾细胞中产生的量处于同一水平。此外,通过使用S1核酸酶保护法,我们比较了(i)转化细胞、(ii)流产感染的小鼠细胞以及(iii)裂解周期后期产生的晚期mRNA的5'端。流产感染细胞和转化细胞中晚期mRNA的5'端比裂解周期中产生的晚期mRNA的5'端异质性更低;然而,它们是裂解周期中产生的晚期转录本5'端的一个子集。