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noIXWBTUV的转录组织与表达,noIXWBTUV是一个调控费氏中华根瘤菌USDA257对大豆品种特异性结瘤的基因座。

Transcriptional organization and expression of noIXWBTUV, a locus that regulates cultivar-specific nodulation of soybean by Rhizobium fredii USDA257.

作者信息

Kovács L G, Balatti P A, Krishnan H B, Pueppke S G

机构信息

Department of Plant Pathology, University of Missouri, Columbia 65211, USA.

出版信息

Mol Microbiol. 1995 Sep;17(5):923-33. doi: 10.1111/j.1365-2958.1995.mmi_17050923.x.

Abstract

Rhizobium fredii is a nitrogen-fixing bacterial symbiont of soybean and a number of other legume species. We have studied the transcriptional organization of a Sym plasmid locus that restricts the host range of R. fredii USDA257 at both the host species and cultivar level. The genes of this host-specificity locus, noIXWBTUV, are transcribed from three promoters. Two of these, which are upstream of noIW and noIBTUV, are oriented face to face and initiate transcription at sites that are 14 bp apart. The third lies upstream from noIX. The noIW promoter is constitutive, whereas the noIB and noIX promoters are inducible by flavonoid signals. We have attempted to express genes from this locus in Escherichia coli systems, both in vivo and in vitro. We detected the insert- and orientation-specific expression of two genes, noIX and noIW, but we were unable to obtain expression of noIBTUV. Antiserum raised against NoIT nevertheless detected an abundantly expressed polypeptide of the predicted size in protein extracts of USDA257. This observation, as well as RNA dot blot data from a series of mutants, indicates that noIBTUV is expressed as a single transcriptional unit in R. fredii. Immunological detection of NoIT, and of a second protein, NoIX, was strictly dependent on flavonoid induction. The NoIX protein was larger than the size predicted from the previously published nucleotide sequence, and this led to resequencing and revision of the open reading frame.

摘要

费氏中华根瘤菌是大豆及其他一些豆科植物的固氮共生细菌。我们研究了一个共生质粒位点的转录组织,该位点在宿主物种和品种水平上限制了费氏中华根瘤菌USDA257的宿主范围。这个宿主特异性位点的基因noIXWBTUV由三个启动子转录。其中两个位于noIW和noIBTUV上游,它们面对面排列,并在相距14 bp的位点起始转录。第三个位于noIX上游。noIW启动子是组成型的,而noIB和noIX启动子可被类黄酮信号诱导。我们试图在大肠杆菌系统中体内和体外表达该位点的基因。我们检测到了两个基因noIX和noIW的插入和方向特异性表达,但未能获得noIBTUV的表达。然而,针对NoIT产生的抗血清在USDA257的蛋白提取物中检测到了一条预测大小的高表达多肽。这一观察结果以及一系列突变体的RNA斑点杂交数据表明,noIBTUV在费氏中华根瘤菌中作为一个单一转录单元表达。对NoIT和另一种蛋白NoIX的免疫检测严格依赖于类黄酮诱导。NoIX蛋白比先前发表的核苷酸序列预测的大小要大,这导致了对开放阅读框的重新测序和修订。

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