Mangel W F, Delius H, Duesberg P H
Proc Natl Acad Sci U S A. 1974 Nov;71(11):4541-5. doi: 10.1073/pnas.71.11.4541.
The structure and molecular weight of the 60-70S RNA complex and the 30-40S RNA species of Rous sarcoma virus were analyzed in an electron microscope after treatment of the RNAs with the bacteriophage T4 gene-32 protein to stretch out the RNA strands. Although all RNA preparations treated with gene-32 protein showed considerable heterogeneity in length, a significant fraction of the RNA retained its original sedimentation coefficient after treatment to allow the following conclusions to be made: The 30-40S RNA was confirmed to be a linear polynucleotide with a molecular weight of about 3 x 10(6). The 60-70S RNA exhibited a network structure with a molecular weight predominantly of about 6 x 10(6). Therefore, the subunit hypothesis for the 60-70S RNA is confirmed. A model for the structure and molecular weight of the 60-70S RNA postulates that the complex consists of two 30-40S RNA subunits held together at many points. This model elucidates the biological observation that the infectivity of RNA tumor viruses is proportional to the amount of 30-40S RNA in a virus preparation and not to the amount of 60-70S RNA.
用噬菌体T4基因32蛋白处理劳斯肉瘤病毒的RNA,使其RNA链伸展后,在电子显微镜下分析了60 - 70S RNA复合物和30 - 40S RNA种类的结构和分子量。尽管用基因32蛋白处理的所有RNA制剂在长度上都表现出相当大的异质性,但相当一部分RNA在处理后仍保留其原来的沉降系数,从而可以得出以下结论:30 - 40S RNA被确认为是一种分子量约为3×10⁶的线性多核苷酸。60 - 70S RNA呈现出一种网络结构,其分子量主要约为6×10⁶。因此,60 - 70S RNA的亚基假说是成立的。一个关于60 - 70S RNA结构和分子量的模型假定,该复合物由两个在多个点结合在一起的30 - 40S RNA亚基组成。这个模型解释了生物学上的一个观察结果,即RNA肿瘤病毒的感染性与病毒制剂中30 - 40S RNA的量成正比,而与60 - 70S RNA的量无关。