Manor H, Wu M, Baran N, Davidson N
J Virol. 1979 Oct;32(1):293-303. doi: 10.1128/JVI.32.1.293-303.1979.
The polyoma virus (Py) RNA species transcribed from the L DNA strand of the "late" region of the Py genome in Py-infected mouse cells have been mapped by hybridization with specific fragments of Py DNA followed by electron microscopic visualization of the hybrids. Total cellular polyadenylated Py-specific RNA molecules having an S value in the range of 16S to 20S were purified by oligodeoxythymidylic acidcellulose column chromatography, preparative hybridization with Py DNA, and sucrose gradient centrifugation. Cytoplasmic Py-specific RNA was similarily purified, except that it was not fractionated by sucrose gradient centrifugation. Hybrids of these RNA molecules and Py DNA fragments were spread for electron microscopy by either the cytochrome c technique or the bacteriophage T4 gene 32 protein method. The polyadenylic acid at the 3'-end of the RNA in the hybrids was identified by labeling with simian virus 40 DNA circles to which polybromodeoxyuridylic acid tails had been covalently attached. These experiments revealed the presence of three L DNA strand transcripts in both RNA preparations. Two of these RNA molecules were found to be spliced from chains transcribed from two noncontiguous parts of the late region. The third molecule either is a continuous transcript of the entire late region or contains a splicing feature which is too small to be reliably observed by the electron microscope methods used. The 5'-ends of the three RNA species map within a region extending from 68 to 70 map units on the Py restriction endonuclease map. Each of the two spliced molecules contains a 5'-terminal leader sequence transcribed from a DNA segment with an estimated length of 60 to 110 nuvleotides. The 3'-ends of the leaders map at 66.7 +/- 1.0 and 66.4 +/- 0.50 map units. In these molecules the 5'-ends of the other part (the main body) map at 59.4 +/- 0.90 and 49.4 +/- 2.0 map units, respectively. The 3'-termini of all three RNA species map at 24 to 25 map units.
在多瘤病毒(Py)感染的小鼠细胞中,从Py基因组“晚期”区域的L DNA链转录而来的多瘤病毒RNA种类,已通过与Py DNA的特定片段杂交,随后对杂交体进行电子显微镜观察来进行定位。通过寡聚脱氧胸苷酸纤维素柱层析、与Py DNA的制备性杂交以及蔗糖梯度离心,纯化了总细胞中具有16S至20S S值范围的多聚腺苷酸化Py特异性RNA分子。细胞质Py特异性RNA以类似方式纯化,只是未通过蔗糖梯度离心进行分级分离。这些RNA分子与Py DNA片段的杂交体,通过细胞色素c技术或噬菌体T4基因32蛋白方法铺展用于电子显微镜观察。通过用共价连接有多溴脱氧尿苷酸尾巴的猿猴病毒40 DNA环进行标记,鉴定了杂交体中RNA 3'端的多聚腺苷酸。这些实验揭示了两种RNA制剂中均存在三种L DNA链转录本。发现其中两个RNA分子是从晚期区域两个不连续部分转录的链中剪接而来。第三个分子要么是整个晚期区域的连续转录本,要么包含一个太小而无法通过所用电子显微镜方法可靠观察到的剪接特征。这三种RNA种类的5'端位于Py限制性内切酶图谱上从68至70图谱单位延伸的区域内。两个剪接分子中的每一个都包含一个从估计长度为60至110个核苷酸的DNA片段转录而来的5'端前导序列。前导序列的3'端位于66.7±1.0和66.4±0.50图谱单位处。在这些分子中,另一部分(主体)的5'端分别位于59.4±0.90和49.4±2.0图谱单位处。所有三种RNA种类的3'末端位于24至25图谱单位处。