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Simian virus 40 early mRNAs in lytically infected and transformed cells contain six 5-terminal caps.

机译:经裂解感染和转化的细胞中的猿猴病毒40早期mRNA包含六个5端帽。

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摘要

Late simian virus 40 (SV40) mRNA contains eight different cap structures which we have previously identified and mapped on the viral genome. As reported here, 5'-cap heterogeneity is a common feature to both the early and the late SV40 mRNA's. methyl-3H-labeled viral mRNA was purified from cells infected at 41 degrees C with SV40 mutant tsA209. Three different cap cores were identified: m7GpppGm, m7GpppCm, and m7GpppAm. An average of three to four m6A residues per mRNA molecule was found. RNase T2-resistant 32P-labeled early caps from tsA209-infected cells isolated and characterized. Six distinct cap I structures were identified: m7GpppCmpU (30%), m7GpppGmpC (24%), m7GpppAmpG (18%), m7GpppGmpU (13%), m7GpppGmpG (12%), and m7GpppAmpU (3%). A similar 5'-end heterogeneity was observed in early SV40 mRNA from BSC-1 cells infected with wild-type SV40 strain 777 in the presence of cytosine arabinoside and in the SV40 UV-transformed permissive line C-6. Five of these capped dinucleotides are complementary to DNA sequences at 0.66 map unit in a region previously identified by the primer extension method (Reddy et al., J. Virol. 30:279-296, 1979; Thompson et al., J. Virol. 31:437-438, 1979) as the 5' end of the early message. DNA sequences upstream from this region contain the TATTTAT (Hogness-Goldberg box), which is missing from upstream of the 5'-cap sites of late SV40 mRNA. Thus, 5'-end heterogeneity is not necessarily related to the presence or the absence of this putative transcriptional "initiation signal." When the possibility that SV40 5' caps represent transcriptional initiation sites is considered, the data also suggest that, on SV40 DNA, eucaryotic RNA polymerase II initiates transcription at multiple nucleotide sequences, including pyrimidines.
机译:猿猴晚期病毒40(SV40)mRNA包含八个不同的帽结构,这些帽结构我们之前已经确定并定位在病毒基因组上。如此处报道的,5'-cap异质性是早期和晚期SV40 mRNA的共同特征。从在41摄氏度下用SV40突变体tsA209感染的细胞中纯化甲基3H标记的病毒mRNA。确定了三个不同的电容芯:m7GpppGm,m7GpppCm和m7GpppAm。每个mRNA分子平均发现3-4个m6A残基。从tsA209感染的细胞中分离并鉴定了耐RNase T2的32P标记的早期帽。确定了六个不同的Cap I结构:m7GpppCmpU(30%),m7GpppGmpC(24%),m7GpppAmpG(18%),m7GpppGmpU(13%),m7GpppGmpG(12%)和m7GpppAmpU(3%)。在胞嘧啶阿拉伯糖苷存在下和在SV40 UV转化的许可系C-6中,在野生型SV40株777感染的BSC-1细胞的早期SV40 mRNA中观察到了相似的5'端异质性。这些加帽的二核苷酸中的五个在先前通过引物延伸方法鉴定的区域(Reddy等人,J。Virol。30:279-296,1979; Thompson等人,J。Virol (1979年31:437-438)作为早期信息的5'末端。该区域上游的DNA序列包含TATTTAT(Hogness-Goldberg框),该序列在晚期SV40 mRNA 5'-cap位点的上游缺失。因此,5'末端异质性不一定与该假定的转录“起始信号”的存在或不存在有关。当考虑到SV40 5'帽代表转录起始位点的可能性时,数据还表明,在SV40 DNA上,真核RNA聚合酶II在包括嘧啶的多个核苷酸序列上起始转录。

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