Majumder H K, Bishayee S, Chakraborty P R, Maitra U
Proc Natl Acad Sci U S A. 1977 Nov;74(11):4891-4. doi: 10.1073/pnas.74.11.4891.
In vitro transcription of T3 DNA by T3 phage-induced RNA polymerase (nucleosidetriphosphate:RNA nucleotidyltransferase; EC 2.7.7.6) yields eight discrete RNAs (designated I-VIII) with molecular weights of approximately 6.2, 4.7, 4, 2.8, 1.8, 0.9, 0.52, and 0.21 X 10(6), respectively. Comparison of the size of in vitro T3 RNA polymerase transcripts with in vivo late T3 mRNAs indicates that several late RNAs produced in T3-infected cells do not correspond to any of the in vitro RNAs, and no RNAs as large as the three largest in vitro RNA species, I, II, and III, are observed. Escherichia coli RNase III cleaves these three high molecular weight T3 RNA polymerase transcripts to discrete RNAs that comigrate in polyacrylamide gel electrophoresis with some of the late T3 RNAs.
用T3噬菌体诱导的RNA聚合酶(核苷三磷酸:RNA核苷酸基转移酶;EC 2.7.7.6)对T3 DNA进行体外转录,产生了8种离散的RNA(命名为I - VIII),分子量分别约为6.2、4.7、4、2.8、1.8、0.9、0.52和0.21×10⁶。将体外T3 RNA聚合酶转录本的大小与体内晚期T3 mRNA的大小进行比较,结果表明,T3感染细胞中产生的几种晚期RNA与任何一种体外RNA都不对应,并且未观察到与体外最大的三种RNA(I、II和III)一样大的RNA。大肠杆菌RNase III将这三种高分子量的T3 RNA聚合酶转录本切割成离散的RNA,这些RNA在聚丙烯酰胺凝胶电泳中与一些晚期T3 RNA迁移率相同。