首页> 外文OA文献 >RNA polymerase II is capable of pausing and prematurely terminating transcription at a precise location in vivo and in vitro.
【2h】

RNA polymerase II is capable of pausing and prematurely terminating transcription at a precise location in vivo and in vitro.

机译:RNA聚合酶II能够在体内和体外的精确位置暂停并过早终止转录。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

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.
机译:通过使用小鼠的微小病毒,我们已经显示出体内和体外RNA聚合酶II在P4启动子下游特定位置142-147个核苷酸处暂停或过早终止转录。发现减毒的RNA并在感染后晚期在A9细胞中在核和细胞质部分中进行体内定位,并且末端核苷酸显示具有3'OH基团。减毒RNA的3'端能够形成发夹结构,然后延伸一段尿苷。为了区分减毒RNA是否由于加工,暂停或终止而形成,并分析其形成所涉及的结构元件,因子或机制,我们使用了体外系统:HeLa的分离核和无细胞提取物细胞。体外研究的结果表明,减毒的RNA是暂停或终止而不是加工的结果。另外,在终止过程中涉及盐溶性因子和RNA二级结构。

著录项

  • 作者

    Resnekov, O; Aloni, Y;

  • 作者单位
  • 年度 1989
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号