Resnekov O, Aloni Y
Department of Genetics, Weizmann Institute of Science, Rehovot, Israel.
Proc Natl Acad Sci U S A. 1989 Jan;86(1):12-6. doi: 10.1073/pnas.86.1.12.
By using the minute virus of mice, we have shown that in vivo and in vitro RNA polymerase II pauses or prematurely terminates transcription at a specific location 142-147 nucleotides downstream from the P4 promoter. The attenuated RNA was found and mapped in vivo in A9 cell late after infection in both the nuclear and cytoplasmic fractions, and the terminal nucleotide was shown to have a 3' OH group. The 3' end of the attenuated RNA is capable of forming a hairpin structure that is followed by a stretch of uridines. To distinguish whether the attenuated RNA is formed as a result of processing, pausing, or termination and to dissect structural elements, factors, or mechanisms that are involved in its formation, we used in vitro systems: isolated nuclei and cell-free extracts from HeLa cells. The results of the in vitro studies show that the attenuated RNA is a result of pausing or termination and not processing. Additionally, a salt-soluble factor and RNA secondary structure were implicated in the process of termination.
通过使用小鼠微小病毒,我们已经表明,在体内和体外,RNA聚合酶II在P4启动子下游142 - 147个核苷酸的特定位置暂停或过早终止转录。在感染后期的A9细胞核和细胞质组分中均发现并定位了体内衰减的RNA,并且末端核苷酸显示具有3' OH基团。衰减RNA的3'端能够形成一个发夹结构,其后跟着一段尿苷序列。为了区分衰减RNA是由加工、暂停还是终止形成的,并剖析参与其形成的结构元件、因子或机制,我们使用了体外系统:从HeLa细胞中分离的细胞核和无细胞提取物。体外研究结果表明,衰减RNA是暂停或终止的结果,而非加工的结果。此外,一种盐溶性因子和RNA二级结构与终止过程有关。