Hecht R M, Pettijohn D E
Nucleic Acids Res. 1976 Mar;3(3):767-88. doi: 10.1093/nar/3.3.767.
Methods are developed for studying RNA molecules bound directly to DNA in bacterial nucleoids. It is found that among the 1000-3000 nascent RNA chains that normally are attached to the DNA via their associated RNA polymerase molecules, 74 +/- 14 chains per nucleoid can be bound differently. These chains unlike the other nascent RNAs remained bound to the DNA after the chromosome was deproteinized and sheared. Sensitive assays using radioactive labels detected no RNA polymerase involved in the RNA-DNA linkage. The linkage was stable at low temperatures, but the RNA separated from the DNA at high temperature. The bound RNA molecules were heterodisperse (weight average length 1200 bases). Pulse-chase experiments and studies of the fate of these RNA molecules in rifampicin treated cells demonstrated that they are nascent RNAs, degraded or released from the DNA in vivo with kinetics similar to that of the total nascent RNA. Hybridization analyses showed that the chains are composed at least in part of nascent rRNA and known mRNA molecules. Some, but not more than 5% of the bound chains, contained sequences of about 300 nucleotides in length, bound to the DNA in an RNase resistant form.
已开发出用于研究直接与细菌类核中的DNA结合的RNA分子的方法。研究发现,在通常通过其相关的RNA聚合酶分子与DNA相连的1000 - 3000条新生RNA链中,每个类核有74±14条链可以以不同方式结合。与其他新生RNA不同,在染色体脱蛋白和剪切后,这些链仍与DNA结合。使用放射性标记的灵敏检测未发现RNA - DNA连接中有RNA聚合酶参与。该连接在低温下稳定,但RNA在高温下与DNA分离。结合的RNA分子是异质的(重均长度为1200个碱基)。脉冲追踪实验以及对这些RNA分子在利福平处理细胞中的命运的研究表明,它们是新生RNA,在体内从DNA降解或释放的动力学与总新生RNA相似。杂交分析表明,这些链至少部分由新生rRNA和已知的mRNA分子组成。一些但不超过5%的结合链包含长度约为300个核苷酸的序列,以抗核糖核酸酶的形式与DNA结合。