首页> 外文期刊>Nucleic Acids Research >In vitro transcription of a poly(dA) centre dot poly(dT)-containing sequence is inhibited by interaction between the template and its transcripts
【24h】

In vitro transcription of a poly(dA) centre dot poly(dT)-containing sequence is inhibited by interaction between the template and its transcripts

机译:模板及其转录物之间的相互作用抑制了含多聚腺苷酸中心点聚多聚腺苷酸的序列的体外转录

获取原文
获取原文并翻译 | 示例
           

摘要

Transcription of poly(dA) centre dot poly(dT)-containing sequences was investigated in vitro using plasmids carrying a (dA)_(34) centre dot (dT)_(34) tract in the coding region of the lacZ gene. The efficiency of transcription of the (dT)_(34) sequence on the transcribing strand by Escherichia coli RNA polymerase was substantially lower (-60%) than that of the (dA)_(34) sequence or of the control lacZ gene. Analysts of the transcription process of the (dT)_(34) sequence by T3 RNA polymerase showed that the transcription was frequently arrested or terminated at the middle as well as immediately proximal of the (dA)_(34) centre dot (dT)_(34) tract, and it occurred more prominently following accumulation of transcription products. This inhibition was strongly enhanced by the addition of the oligonucleotide (dT)_(34) or poly(U) to the reaction mixture, while (dA)_(34) and the duplex (dA)_(34) centre dot (dT)_(34) suppressed the inhibition. A similar transcriptional inhibition was also observed in transcription mediated by T7 RNA polymerase and eukaryotic RNA poiymerase II. We also demonstrated RNA centre dot DNA complex formation of the (dA)_(34) centre dot (dT)_(34) tract with poly(U), but not with poly(A). These findings strongly suggest that poly(dT)-containing template sequences interact and form a complex with its transcription products, possibly an RNA centre dot DNA triplex, which blocks further transcription. This would explain the instability of the piasmids transcribing mRNAs with poly(U) but not poly(A) tracts and the underrepresentation of poly(U) but not poly(A) tracts in mRNAs.
机译:使用在lacZ基因的编码区带有(dA)_(34)中心点(dT)_(34)的质粒在体外研究了含poly(dA)中心点的poly(dT)序列的转录。大肠杆菌RNA聚合酶在转录链上转录(dT)_(34)序列的效率显着低于(dA)_(34)序列或对照lacZ基因的转录效率(-60%)。 T3 RNA聚合酶对(dT)_(34)序列转录过程的分析表明,该转录经常在(dA)_(34)中心点(dT)的中间以及近端终止或终止。 _(34)道,它在转录产物积累后更明显地发生。通过向反应混合物中添加寡核苷酸(dT)_(34)或poly(U),而(dA)_(34)和双链体(dA)_(34)中心点(dT)加入,可大大增强这种抑制作用)_(34)抑制了抑制作用。在由T7 RNA聚合酶和真核RNA聚合酶II介导的转录中也观察到类似的转录抑制作用。我们还证明了(dA)_(34)中心点(dT)_(34)的RNA中心点DNA复合物与poly(U)形成,但与poly(A)无关。这些发现强烈表明,含有聚(dT)的模板序列与其转录产物相互作用,并形成复合物,该转录产物可能是阻止进一步转录的RNA中心点DNA三链体。这可以解释用聚(U)而非聚(A)束转录mRNA的质粒的不稳定性,以及在mRNA中聚(U)而非聚(A)束的代表性不足。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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