Daniell E, Fedor M J
Proc Natl Acad Sci U S A. 1982 Mar;79(6):1834-8. doi: 10.1073/pnas.79.6.1834.
Intact cores of adenovirus type 5 were transcribed in vitro in extracts derived from uninfected HeLa cells, and the products were analyzed by hybridization to restricted viral DNA. Predominant transcripts from cores were distinctly different from transcripts generated from deproteinized DNA. The extracts contained RNA polymerases II and III. Transcription from cores was completely inhibited by low levels of alpha-amanitin, and there was little or no hybridization of products to the region of the genome encoding the small polymerase III-dependent virus-associated RNA that was a major transcript from the DNA template. The major transcripts from cores hybridized to the rightward-transcribed strand of the region between 75 and 89 map units, early region 3 of the adenovirus genome. There was several-fold more transcription of this region in cores than of the region downstream from the major late promoter, which predominates among polymerase II transcripts from DNA.
5型腺病毒的完整核心在未感染的HeLa细胞提取物中进行体外转录,转录产物通过与限制性病毒DNA杂交进行分析。核心的主要转录本与脱蛋白DNA产生的转录本明显不同。提取物中含有RNA聚合酶II和III。核心转录被低水平的α-鹅膏蕈碱完全抑制,产物与基因组中编码小的聚合酶III依赖性病毒相关RNA的区域几乎没有杂交,而该区域是DNA模板的主要转录本。核心的主要转录本与腺病毒基因组早期区域3中75至89个图距单位之间区域的右向转录链杂交。核心中该区域的转录比主要晚期启动子下游区域的转录多几倍,而主要晚期启动子在DNA的聚合酶II转录本中占主导地位。