Attenuation may regulate gene expression in animal viruses and cells.

Y Aloni, N Hay
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引用次数: 27

Abstract

In eukaryotes, an abundant population of promoter-proximal RNA chains have been observed and studied, mainly in whole nuclear RNA, in denovirus type 2, and in SV40. On the basis of these results it has been suggested that a premature termination process resembling attenuation in prokaryotes occurs in eukaryotes. Moreover, these studies have shown that the adenosine analog 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole (DRB) enhances premature termination, but its mode of action is not understood. The determination of the nucleotide sequences of SV40 and other viruses and cellular genes provide means for elucidating the nucleotide sequences involved in the attenuation mechanism. A model has recently been described in which attenuation and mRNA modulation in a feedback control system quantitatively regulate SV40 gene expression. The suggested mechanism described in this model opens up approaches to the investigation of attenuation and mRNA modulation as a possible mechanism whereby eukaryotes may regulate transcription in a variety of different circumstances.

衰减可能调节动物病毒和细胞中的基因表达。
在真核生物中,已经观察和研究了大量的启动子-近端RNA链,主要是在全核RNA中,在2型病毒和SV40中。在这些结果的基础上,提出了一个类似于原核生物衰减的过早终止过程发生在真核生物中。此外,这些研究表明腺苷类似物5,6-二氯-1- β -d -核糖呋喃基苯并咪唑(DRB)可促进过早终止,但其作用方式尚不清楚。SV40和其他病毒及细胞基因核苷酸序列的测定为阐明参与衰减机制的核苷酸序列提供了手段。最近描述了一个模型,其中反馈控制系统中的衰减和mRNA调制定量调节SV40基因表达。该模型中描述的机制为研究衰减和mRNA调节作为真核生物在各种不同情况下调节转录的可能机制开辟了途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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