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转录暂停对色氨酸操纵子前导序列衰减作用的理论评估

Theoretical evaluation of transcriptional pausing effect on the attenuation in trp leader sequence.

作者信息

Suzuki H, Kunisawa T, Otsuka J

出版信息

Biophys J. 1986 Feb;49(2):425-35. doi: 10.1016/S0006-3495(86)83652-9.

Abstract

The effect of transcriptional pausing on attenuation is investigated theoretically on the basis of the attenuation control mechanism presented by Oxender et al. (Oxender, D. L., G. Zurawski, and C. Yanofsky, 1979, Proc. Natl. Acad. Sci. USA. 76:5524-5528). An extended stochastic model including the RNA polymerase pausing in the leader region is developed to calculate the probability of relative position between the RNA polymerase transcribing the trp leader sequence and the ribosome translating the transcript. The present study results in a new rationale that the transcriptional pausing site in the leader sequence makes the attenuation control both more sensitive as an on/off switch and less sensitive to variations in the concentration of cellular metabolites not connected with the need for expressing, or not expressing, the particular operon. It is also proposed that the transcriptional pausing diminishes the dependence of attenuation control characteristics on the number of nucleotides in the leader sequence. This result may be useful for understanding the attenuation control efficiencies of other amino acid leader sequences with different lengths of nucleotides.

摘要

基于奥克森德等人(Oxender, D. L., G. Zurawski, and C. Yanofsky, 1979, Proc. Natl. Acad. Sci. USA. 76:5524 - 5528)提出的衰减控制机制,从理论上研究了转录暂停对衰减的影响。开发了一个扩展的随机模型,该模型包括RNA聚合酶在前导区的暂停,以计算转录色氨酸前导序列的RNA聚合酶与翻译转录本的核糖体之间相对位置的概率。本研究得出了一个新的理论依据,即前导序列中的转录暂停位点使衰减控制作为一种开/关开关更加敏感,同时对与特定操纵子表达或不表达需求无关的细胞代谢物浓度变化不太敏感。还提出转录暂停降低了衰减控制特性对前导序列中核苷酸数量的依赖性。这一结果可能有助于理解其他具有不同核苷酸长度的氨基酸前导序列的衰减控制效率。

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