Tamm I, Kikuchi T
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5750-4. doi: 10.1073/pnas.76.11.5750.
Labeling of RNA in isolated HeLa cell nuclei in vitro reveals an abundance of short RNA chains made by RNA polymerase II. These short chains were initiated prior to isolation of the nuclei. The short abundant chains are increased in amount in nuclei isolated from cells treated with 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole (DRB). Kinetic evidence indicates that the bulk of the putative heterogeneous nuclear RNA (hnRNA) precursor molecules that are terminated early in vivo are terminated approximately 100-300 nucleotides from sites of initiation. DRB increases the frequency of early termination, but there is a fraction of hnRNA precursor molecules whose elongation is not affected by DRB. Heparin is useful in studies of hnRNA transcription in isolated nuclei because it enhances chain elongation.
体外对分离的HeLa细胞核中的RNA进行标记,结果显示RNA聚合酶II合成了大量短RNA链。这些短链在细胞核分离之前就已起始合成。在用5,6-二氯-1-β-D-呋喃核糖基苯并咪唑(DRB)处理的细胞中分离得到的细胞核中,短链丰富的RNA数量增加。动力学证据表明,在体内早期终止的大部分假定的不均一核RNA(hnRNA)前体分子,是在起始位点约100 - 300个核苷酸处终止的。DRB增加了早期终止的频率,但有一部分hnRNA前体分子的延伸不受DRB影响。肝素在研究分离细胞核中的hnRNA转录时很有用,因为它能增强链延伸。