Suppr超能文献

转录终止因子ρ在以合成脱氧核糖核酸为模板的模型转录系统中的功能。

Function of transcription termination factor rho in a model transcription system using synthetic deoxyribonucleic acid as template.

作者信息

Shigesada K, Imai M

出版信息

Biochemistry. 1982 Nov 9;21(23):5849-56. doi: 10.1021/bi00266a019.

Abstract

The function of a transcription termination factor, rho, has been studied by using several synthetic DNAs with simple repetitive base sequences as templates for transcription. rho actually exhibits various effects on transcription depending on the base sequence of the template: (1) rho terminates poly(A) synthesis with poly(dA) x poly(dT), poly(dT), or oligo(dT), leading to release of RNA from RNA polymerase. rho also inhibits the synthesis of other homoribopolymers such as poly(U) directed by poly(dA) x poly(dT) and poly(C) and poly(I) directed by poly(dG) x poly(dC), presumably by a similar mechanism. (2) rho inhibits the synthesis of another homoribopolymer, poly(G), directed by poly(dG) x poly(dC) at the step of initiation rather than propagation of transcription. (3) rho stimulates rather than inhibits the synthesis of poly(A-C) and poly(G-U) directed by poly[d(A-C)] x poly[d(G-T)], presumably by enhancing the dissociation of transcription complexes. (4) rho has no influence on the synthesis of poly(A-U) and poly(G-C) directed by poly[d(A-T)] and poly[d(G-C)], respectively. In the first case, but not otherwise, the effect of rho is coupled with its RNA-dependent nucleosidetriphosphate phosphohydrolase activity, as is rho-mediated transcription termination on natural templates. The implication of these results is discussed in reference to the current view that rho acts on transcription complexes that have ceased elongation and causes release of RNA in an energy-requiring reaction.

摘要

通过使用几种具有简单重复碱基序列的合成DNA作为转录模板,对转录终止因子ρ的功能进行了研究。实际上,ρ对转录的影响因模板的碱基序列而异:(1)ρ以聚(dA)×聚(dT)、聚(dT)或寡聚(dT)终止聚(A)合成,导致RNA从RNA聚合酶中释放。ρ还抑制其他同聚核糖核酸的合成,例如由聚(dA)×聚(dT)指导的聚(U)以及由聚(dG)×聚(dC)指导的聚(C)和聚(I),推测是通过类似的机制。(2)ρ在转录起始而非延伸步骤抑制由聚(dG)×聚(dC)指导的另一种同聚核糖核酸聚(G)的合成。(3)ρ刺激而非抑制由聚[d(A-C)]×聚[d(G-T)]指导的聚(A-C)和聚(G-U)的合成,推测是通过增强转录复合物的解离。(4)ρ分别对由聚[d(A-T)]和聚[d(G-C)]指导的聚(A-U)和聚(G-C)的合成没有影响。在第一种情况下,与其他情况不同,ρ的作用与其RNA依赖性核苷三磷酸磷酸水解酶活性相关联,天然模板上的ρ介导的转录终止也是如此。参考当前认为ρ作用于已停止延伸的转录复合物并在耗能反应中导致RNA释放的观点,对这些结果的意义进行了讨论。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验