May E, Maizel J V, Salzman N P
Proc Natl Acad Sci U S A. 1977 Feb;74(2):496-500. doi: 10.1073/pnas.74.2.496.
Simian virus 40 (SV40) late 19S and 16S mRNAs were annealed to complementary regions of partially melted viral double-stranded SV40(LHpa II) DNA or SV40(LBam HI) DNA. The RNA-DNA hybrid regions within the DNA molecules were visualized as loops [with SV40(LBam HI) DNA] in the electron microscope. The data confirm the previous localizations of the 3' and 5' ends of 16S SV40 mRNA and of the 3' end of late 19S SV40 mRNA. The 5' end of the major stable SV40 late 19S mRNA has been positioned at 0.755 map unit. Thus, the sequences of viral DNA from 0.655 to 0.755 map unit, including the replication origin, are not converted into major stable species of late viral mRNA.
将猴病毒40(SV40)晚期19S和16S mRNA与部分解链的病毒双链SV40(LHpa II)DNA或SV40(LBam HI)DNA的互补区域进行退火。DNA分子内的RNA-DNA杂交区域在电子显微镜下呈现为环(对于SV40(LBam HI)DNA)。这些数据证实了先前对16S SV40 mRNA的3'和5'末端以及晚期19S SV40 mRNA的3'末端的定位。主要稳定的SV40晚期19S mRNA的5'末端位于0.755图谱单位处。因此,从0.655到0.755图谱单位的病毒DNA序列,包括复制起点,不会转化为晚期病毒mRNA的主要稳定种类。