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利用前导-弱化子-galK基因融合分析ilvGMEDA操纵子的调控

Analysis of regulation of the ilvGMEDA operon by using leader-attenuator-galK gene fusions.

作者信息

Lawther R P, Lopes J M, Ortuno M J, White M C

机构信息

Department of Biological Sciences, University of South Carolina, Columbia 29208.

出版信息

J Bacteriol. 1990 May;172(5):2320-7. doi: 10.1128/jb.172.5.2320-2327.1990.

Abstract

Five of the genes for the biosynthesis of isoleucine and valine form the ilvGMEDA operon of Escherichia coli K-12. Expression of the operon responds to changes in the availability of isoleucine, leucine, and valine (ILV). Addition of an excess of all three amino acids results in reduced expression of the operon, whereas limitation for one of the three amino acids causes an increase in expression. The operon is preceded by a leader-attenuator which clearly regulates the increased expression that occurs due to reduced aminoacylation of tRNA. To assess the factors that result in the reduced expression of this operon upon the addition of ILV, a series of plasmids were constructed in which the ilv regulatory region was fused to galK. In response to addition of the amino acids, expression of the galK gene fused to the leader-attenuator decreased five- to sevenfold, instead of the twofold observed for the chromosomal operon. A deletion analysis with these plasmids indicated that the ILV-specific decrease in expression required an intact leader-attenuator but not ilvGp2 or the DNA that precedes this promoter. This conclusion was supported by both S1 nuclease analysis of transcription initiation and determination of galK mRNA levels by RNA-RNA hybridization.

摘要

用于异亮氨酸和缬氨酸生物合成的五个基因构成了大肠杆菌K-12的ilvGMEDA操纵子。该操纵子的表达会对异亮氨酸、亮氨酸和缬氨酸(ILV)的可利用性变化做出反应。添加过量的这三种氨基酸会导致该操纵子的表达降低,而对这三种氨基酸中的一种进行限制则会导致表达增加。该操纵子之前有一个前导衰减子,它明显调控因tRNA氨基酰化减少而发生的表达增加。为了评估在添加ILV后导致该操纵子表达降低的因素,构建了一系列质粒,其中ilv调控区与galK融合。响应氨基酸的添加,与前导衰减子融合的galK基因的表达降低了五到七倍,而不是在染色体操纵子中观察到的两倍。用这些质粒进行的缺失分析表明,ILV特异性的表达降低需要完整的前导衰减子,但不需要ilvGp2或该启动子之前的DNA。转录起始的S1核酸酶分析以及通过RNA-RNA杂交测定galK mRNA水平均支持了这一结论。

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