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大肠杆菌中七个核糖体RNA操纵子表达的比较。

Comparison of the expression of the seven ribosomal RNA operons in Escherichia coli.

作者信息

Condon C, Philips J, Fu Z Y, Squires C, Squires C L

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027.

出版信息

EMBO J. 1992 Nov;11(11):4175-85. doi: 10.1002/j.1460-2075.1992.tb05511.x.

Abstract

We have compared the expression of the seven ribosomal RNA operons (rrn) of Escherichia coli and their responses to a variety of physiological and genetic perturbations. We used a set of rrn promoter fusion constructs in their native chromosomal positions to examine effects of chromosomal location on rrn operon expression and the same set of fusions on lambda lysogens to assay intrinsic promoter strengths independent of chromosome context. In its native chromosomal location, expression of the rrnH operon was significantly lower than expected. This effect was not attributable to weak promoter activity and was dependent on the growth medium. The rrnE operon had reduced promoter activity relative to the other ribosomal operons in minimal medium and thus appears to have abnormal growth rate regulation. The ribosomal RNA operons showed varied responses to amino acid starvation; expression of rrnD was inhibited most. There was only a slight increase in rrn transcription in response to a temperature shift (30 degrees C to 42 degrees C) and the differences between individual operons was very small. The rrnG operon showed a significantly lower response than the other ribosomal RNA operons to a depletion of the rrn transcription activator, Fis, and thus appears to have decreased Fis-mediated transactivation. Finally, the chromosomal fusion strains were used to study the effect on growth rate of inactivating each rrn operon. In fast growth conditions, loss of certain rrn operons caused subtle decreases in growth rate on complex medium.

摘要

我们比较了大肠杆菌的七个核糖体RNA操纵子(rrn)的表达情况以及它们对各种生理和遗传扰动的反应。我们使用了一组处于其天然染色体位置的rrn启动子融合构建体,来研究染色体位置对rrn操纵子表达的影响,并使用同一组融合构建体对λ溶原菌进行分析,以测定独立于染色体背景的内在启动子强度。在其天然染色体位置,rrnH操纵子的表达明显低于预期。这种效应并非归因于启动子活性较弱,并且依赖于生长培养基。在基本培养基中,rrnE操纵子相对于其他核糖体操纵子具有降低的启动子活性,因此似乎具有异常的生长速率调节。核糖体RNA操纵子对氨基酸饥饿表现出不同的反应;rrnD的表达受到的抑制最大。响应温度变化(从30℃至42℃)时,rrn转录仅有轻微增加,并且各个操纵子之间的差异非常小。rrnG操纵子对rrn转录激活因子Fis的缺失表现出比其他核糖体RNA操纵子明显更低的反应,因此似乎具有降低的Fis介导的反式激活作用。最后,使用染色体融合菌株来研究使每个rrn操纵子失活对生长速率的影响。在快速生长条件下,某些rrn操纵子的缺失会导致在复合培养基上生长速率出现细微下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbed/556928/837166490f47/emboj00096-0359-a.jpg

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