Robertson D L, Varmus H E
J Virol. 1979 May;30(2):576-89. doi: 10.1128/JVI.30.2.576-589.1979.
We have characterized murine mammary tumor virus (MuMTV)-specific RNA in several types of cells in which viral DNA is transcribed into RNA: cultured GR mouse mammary tumor cells, S49 lymphoma cells from BALB/c mice, lactating mammary glands from C57BL/6 mice, and mink lung cells infected in vitro with MuMTV. In all cell types studied, there are three distinct species of intracellular viral RNA, with sedimentation coefficients of 35S, 24S, and 13S (or molecular weights of 3.1 X 10(6), 1.5 X 10(6), and 0.37 X 10(6), as determined by rate-zonal sedimentation in sucrose gradients and by electrophoresis in agarose gels under denaturing conditions. These three viral RNA species appear to be present regardless of viral RNA concentration, responsiveness to glucocorticoid hormones, production of extracellular virus, and use of either endogenous or acquired MuMTV proviral DNA as template. The three viral RNAs display characteristics of mRNAs in that they are polyadenylated, associated with polyribosomes, and released from polyribosomes by treatment with EDTA; hence all three species presumably direct the synthesis of virus-coded proteins. The two larger species of viral RNA are probably responsible for synthesis of the structural proteins of the virion, but the function of the 13S RNA is not known. Both of the subgenomic RNAs contain sequences found at the 3' terminus of 35S (or genomic) RNA. However, only the 24S RNA (not the 13S RNA) contains sequences which are located at the 5' terminus of 35S RNA and are apparently transposed during RNA synthesis of maturation, as described for subgenomic mRNA's of other retroviruses.
我们已经对几种能将病毒DNA转录为RNA的细胞中的鼠乳腺肿瘤病毒(MuMTV)特异性RNA进行了特性分析:培养的GR小鼠乳腺肿瘤细胞、来自BALB/c小鼠的S49淋巴瘤细胞、C57BL/6小鼠的泌乳乳腺以及体外感染MuMTV的貂肺细胞。在所有研究的细胞类型中,存在三种不同的细胞内病毒RNA,沉降系数分别为35S、24S和13S(通过蔗糖梯度速率区带沉降法和变性条件下琼脂糖凝胶电泳测定,其分子量分别为3.1×10⁶、1.5×10⁶和0.37×10⁶)。无论病毒RNA浓度、对糖皮质激素的反应性、细胞外病毒的产生以及以内源或获得性MuMTV前病毒DNA作为模板的情况如何,这三种病毒RNA似乎都存在。这三种病毒RNA具有mRNA的特征,因为它们是多聚腺苷酸化的,与多核糖体相关,并且通过用EDTA处理可从多核糖体上释放出来;因此,这三种RNA可能都指导病毒编码蛋白的合成。两种较大的病毒RNA可能负责病毒粒子结构蛋白的合成,但13S RNA的功能尚不清楚。两种亚基因组RNA都含有在35S(或基因组)RNA 3'末端发现的序列。然而,只有24S RNA(而非13S RNA)含有位于35S RNA 5'末端的序列,并且在RNA合成成熟过程中显然发生了转位,这与其他逆转录病毒的亚基因组mRNA情况类似。