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引发蛋白在复制起点的正负作用。

Positive and negative roles of an initiator protein at an origin of replication.

作者信息

Filutowicz M, McEachern M J, Helinski D R

出版信息

Proc Natl Acad Sci U S A. 1986 Dec;83(24):9645-9. doi: 10.1073/pnas.83.24.9645.

Abstract

The properties of mutants in the pir gene of plasmid R6K have suggested that the pi protein plays a dual role; it is required for replication to occur and also plays a role in the negative control of the plasmid copy number. In our present study, we have found that the pi level in cell extracts of Escherichia coli strains containing R6K derivatives is surprisingly high (approximately equal to 10(4) dimers per cell) and that this level is not altered in cells carrying high copy number pir mutants. The wild-type and a high copy mutant (Cos405) pir gene were inserted downstream of promoters of different strengths to measure the copy number of an R6K gamma replicon as a function of a 1000-fold range of intracellular pi concentrations. The data demonstrate that reducing the intracellular level of pi to 5% of its normal value can result in a substantial increase in copy number of a gamma origin replicon and that a pi level less than 1% of normal is still permissive for replication. Conversely, increasing the pi level even a few-fold above normal results in a marked inhibition of replication of plasmids containing a single, two, or all three of the R6K origins (alpha, beta, and gamma). We have also shown that the replication inhibition mediated by excess pi is greatly reduced by the pir405 Cos mutation. These results demonstrate that the total level of pi protein is not rate-limiting for a gamma replicon. We have also determined the sensitivity of the pir gene promoter to a wide range of pi concentrations. The activity of this promoter is stimulated by very low pi levels and is almost entirely inhibited when the protein is overproduced 2-fold.

摘要

质粒R6K的pir基因中突变体的特性表明,π蛋白具有双重作用;它是复制发生所必需的,并且在质粒拷贝数的负调控中也起作用。在我们目前的研究中,我们发现含有R6K衍生物的大肠杆菌菌株细胞提取物中的π水平出奇地高(约为每个细胞10⁴个二聚体),并且在携带高拷贝数pir突变体的细胞中该水平没有改变。将野生型和高拷贝突变体(Cos405)pir基因插入不同强度启动子的下游,以测量R6Kγ复制子的拷贝数作为细胞内π浓度1000倍范围的函数。数据表明,将细胞内π水平降低至其正常值的5%会导致γ起源复制子的拷贝数大幅增加,并且π水平低于正常水平的1%仍允许复制。相反,将π水平提高到比正常水平高几倍会导致含有R6K的一个、两个或所有三个起源(α、β和γ)的质粒复制受到显著抑制。我们还表明,pir405 Cos突变大大降低了过量π介导的复制抑制。这些结果表明,π蛋白的总水平对γ复制子不是限速的。我们还确定了pir基因启动子对广泛的π浓度的敏感性。该启动子的活性受到非常低的π水平的刺激,当蛋白质过量产生2倍时几乎完全被抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2250/387197/21eed4af9aaf/pnas00328-0381-a.jpg

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