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Tn4652转座酶基因tnpA的表达受到整合宿主因子的正向影响。

Expression of the transposase gene tnpA of Tn4652 is positively affected by integration host factor.

作者信息

Hõrak R, Kivisaar M

机构信息

Estonian Biocentre and Institute of Molecular and Cell Biology, Tartu University, EE2400 Tartu, Estonia.

出版信息

J Bacteriol. 1998 Jun;180(11):2822-9. doi: 10.1128/JB.180.11.2822-2829.1998.

Abstract

Tn4652 is a derivative of the toluene degradation transposon Tn4651 that belongs to the Tn3 family of transposons (M. Tsuda and T. Iino, Mol. Gen. Genet. 210:270-276, 1987). We have sequenced the transposase gene tnpA of transposon Tn4652 and mapped its promoter to the right end of the element. The deduced amino acid sequence of tnpA revealed 96.2% identity with the putative transposase of Tn5041. Homology with other Tn3 family transposases was only moderate (about 20 to 24% identity), suggesting that Tn4652 and Tn5041 are distantly related members of the Tn3 family. Functional analysis of the tnpA promoter revealed that it is active in Pseudomonas putida but silent in Escherichia coli, indicating that some P. putida-specific factor is required for the transcription from this promoter. Additionally, tnpA promoter activity was shown to be modulated by integration host factor (IHF). The presence of an IHF-binding site upstream of the tnpA promoter enhanced the promoter activity. The positive role of IHF was also confirmed by the finding that the enhancing effect of IHF was not detected in the P. putida ihfA-deficient strain A8759. Moreover, the Tn4652 terminal sequences had a negative effect on transcription from the tnpA promoter in the ihfA-defective strain. This finding suggests that IHF not only enhances transcription from the tnpA promoter but also alleviates the negative effect of terminal sequences of Tn4652 on the promoter activity. Also, an in vitro binding assay demonstrated that both ends of Tn4652 bind IHF from a cell lysate of E. coli.

摘要

Tn4652是甲苯降解转座子Tn4651的衍生物,Tn4651属于转座子Tn3家族(M. Tsuda和T. Iino,《分子与普通遗传学》210:270 - 276,1987年)。我们已对转座子Tn4652的转座酶基因tnpA进行了测序,并将其启动子定位到该元件的右端。tnpA推导的氨基酸序列与Tn5041的推定转座酶显示出96.2%的同一性。与其他Tn3家族转座酶的同源性仅为中等水平(约20%至24%的同一性),这表明Tn4652和Tn5041是Tn3家族关系较远的成员。对tnpA启动子的功能分析表明,它在恶臭假单胞菌中具有活性,但在大肠杆菌中无活性,这表明该启动子的转录需要一些恶臭假单胞菌特异性因子。此外,已证明tnpA启动子活性受整合宿主因子(IHF)调节。tnpA启动子上游存在IHF结合位点可增强启动子活性。在恶臭假单胞菌ihfA缺陷菌株A8759中未检测到IHF的增强作用,这一发现也证实了IHF的积极作用。此外,Tn4652末端序列对ihfA缺陷菌株中tnpA启动子的转录有负面影响。这一发现表明,IHF不仅增强了tnpA启动子的转录,还减轻了Tn4652末端序列对启动子活性的负面影响。而且,体外结合试验表明,Tn4652的两端均能与大肠杆菌细胞裂解物中的IHF结合。

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