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不相容性与IncFII质粒复制控制

Incompatibility and IncFII plasmid replication control.

作者信息

Rownd R H, Womble D D, Dong X N, Luckow V A, Wu R P

出版信息

Basic Life Sci. 1985;30:335-54. doi: 10.1007/978-1-4613-2447-8_26.

Abstract

The DNA coding for replication control and incompatibility of the plasmid NR1 serves as a template in vivo and in vitro for RNA transcription in both directions. In the rightward direction, RNA synthesis begins from 2 different promoters, one of which is regulated and the other constitutive. In vivo, each of these transcripts is more than 1,000 nucleotides long, terminating near the estimated site for the origin of replication. These transcripts serve as messenger RNA for several proteins. One protein (repA1) is required for replication and another (repA2) serves as the repressor for the regulated rightward promoter. RNA synthesis in the leftward direction is constitutive and produces a single transcript of 91 nucleotides which is complementary in sequence to the rightward transcripts. This small transcript is the incompatibility product which regulates the replication of the plasmid. When the intracellular concentration of the small transcript is experimentally varied, the rate of translation of the rightward transcripts and the rate of initiation of replication (plasmid copy number) vary inversely to its concentration. The mode of action of this inhibitor RNA is likely to be formation of an RNA-RNA duplex with the rightward transcripts, thereby inhibiting the translation which would produce the required replication protein. The probability that a rightward transcript will escape interaction with the small RNA molecules and thus allow replication to initiate can be predicted from the laws of mass action based on base-stacking free energies for the likely sequences of initial contact. The estimated intracellular RNA concentrations, based on quantitative hybridization experiments, are agreement with those predicted from the calculated equilibrium constants for duplex formation.

摘要

编码质粒NR1复制控制和不相容性的DNA在体内和体外均作为双向RNA转录的模板。在向右的方向上,RNA合成从2个不同的启动子开始,其中一个是受调控的,另一个是组成型的。在体内,这些转录本中的每一个都超过1000个核苷酸长,在估计的复制起点附近终止。这些转录本作为几种蛋白质的信使RNA。一种蛋白质(repA1)是复制所必需的,另一种蛋白质(repA2)作为受调控的向右启动子的阻遏物。向左的RNA合成是组成型的,并产生一个91个核苷酸的单一转录本,其序列与向右的转录本互补。这个小转录本是调节质粒复制的不相容性产物。当通过实验改变小转录本的细胞内浓度时,向右转录本的翻译速率和复制起始速率(质粒拷贝数)与其浓度成反比。这种抑制性RNA的作用方式可能是与向右的转录本形成RNA-RNA双链体,从而抑制产生所需复制蛋白的翻译。根据初始接触可能序列的碱基堆积自由能,基于质量作用定律可以预测向右转录本逃脱与小RNA分子相互作用从而允许复制起始的概率。基于定量杂交实验估计的细胞内RNA浓度与根据双链体形成的计算平衡常数预测的浓度一致。

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