Birg F, Favaloro J, Kamen R
Proc Natl Acad Sci U S A. 1977 Aug;74(8):3138-42. doi: 10.1073/pnas.74.8.3138.
The size and sequence composition of virus-specific RNA extracted from the nuclei of mouse cells late during polyoma virus productive infection were studied by blot-hybridization analysis of 32P-labeled RNA fractionated on CH3HgOH/agarose gels. Viral RNA molecules between approximately 0.4 and 4 times the length of a complete transcript of the 5.4-kilobase circular viral DNA were found. Less than 20% of such molecules were polyadenylylated. Although viral RNA of all sizes contained species that together hybridized to the entire polyoma genome, sequences complementary to the late region were more abundant than sequences complementary to the early region in transcripts less than 10-12 kilobases long.
通过对在CH3HgOH/琼脂糖凝胶上分级分离的32P标记RNA进行印迹杂交分析,研究了在多瘤病毒生产性感染后期从小鼠细胞核中提取的病毒特异性RNA的大小和序列组成。发现病毒RNA分子的长度约为5.4千碱基环状病毒DNA完整转录本长度的0.4至4倍。这类分子中不到20%是聚腺苷酸化的。尽管所有大小的病毒RNA都含有与整个多瘤病毒基因组杂交的物种,但在长度小于10 - 12千碱基的转录本中,与晚期区域互补的序列比与早期区域互补的序列更丰富。