Vennström B, Pettersson U, Philipson L
Nucleic Acids Res. 1978 Jan;5(1):205-19. doi: 10.1093/nar/5.1.205.
Initiation of adenovirus transcription was analyzed by incubation of isolated nuclei from virus infected cells in the presence of beta-32P GTP or beta-32P ATP. Nucleotide analysis of RNA from nuclei incubated with beta-32P GTP shows that the label is incorporated exclusively into pppGp and ppGp. Under similar incubation conditions, the label from beta-32P ATP was incorporated primarily into the 5' phosphate of 5', 3' mononucleoside diphosphates, but label was also detected in pppAp, pppGp and in the 3' nucleoside monophosphates. Analysis of RNA, synthesized in the presence of different concentrations of alpha-amanitin, shows that only RNA polymerase III initiates virus specific transcription in isolated nuclei. The virus specific transcripts containing pppAp and pppGp in their 5' termini were identified as the 5.5S and 5.2S viral RNA species by hybridization and finger printing.
通过在β-32P GTP或β-32P ATP存在的情况下孵育病毒感染细胞的分离细胞核,来分析腺病毒转录的起始。用β-32P GTP孵育的细胞核RNA的核苷酸分析表明,标记仅掺入pppGp和ppGp中。在类似的孵育条件下,β-32P ATP的标记主要掺入5',3'单核苷二磷酸的5'磷酸中,但在pppAp、pppGp和3'核苷单磷酸中也检测到标记。在不同浓度的α-鹅膏蕈碱存在下合成的RNA分析表明,只有RNA聚合酶III在分离的细胞核中起始病毒特异性转录。通过杂交和指纹分析,将其5'末端含有pppAp和pppGp的病毒特异性转录本鉴定为5.5S和5.2S病毒RNA种类。