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一种对有效的植物信号转导必需的染色体根癌土壤杆菌基因。

A chromosomal Agrobacterium tumefaciens gene required for effective plant signal transduction.

作者信息

Huang M L, Cangelosi G A, Halperin W, Nester E W

机构信息

Department of Botany, University of Washington, Seattle 98195.

出版信息

J Bacteriol. 1990 Apr;172(4):1814-22. doi: 10.1128/jb.172.4.1814-1822.1990.

Abstract

The vir gene products of Agrobacterium tumefaciens carry out the transfer of T-DNA to the plant genome. Effective transcriptional induction of the vir genes by plant signal molecules is controlled by two vir gene products, VirA and VirG. In this study we have identified and cloned a chromosomal region which is also required for vir gene induction. Transposon insertions within this region reduce induction significantly and strongly attenuate virulence, resulting in a restricted host range for infection. The reduction in vir gene transcription can be partially overcome by high concentrations of the inducer molecule acetosyringone. Expression of virG at low pH and low phosphate concentrations, which is independent of plant signals, is not affected by these mutations. Sequence analysis of the region revealed two divergent open reading frames, which we have designated chvE and ORF1. Several transposon insertions mapped in chvE; this resulted in attenuated virulence. chvE codes for a putative protein which is homologous to two periplasmic receptor proteins involved in chemotaxis and uptake of sugars. Whether ORF1 is required for virulence is uncertain. One transposon insertion resulting in avirulence maps in or near the 5' end of ORF1, and several which do not affect virulence map in its 3' end. ORF1 codes for a putative protein which is homologous to a family of transcriptional activator proteins.

摘要

根癌土壤杆菌的vir基因产物负责将T-DNA转移至植物基因组。植物信号分子对vir基因的有效转录诱导由两种vir基因产物VirA和VirG控制。在本研究中,我们鉴定并克隆了一个对vir基因诱导也必需的染色体区域。该区域内的转座子插入显著降低诱导作用并强烈减弱毒力,导致感染的宿主范围受限。高浓度的诱导分子乙酰丁香酮可部分克服vir基因转录的降低。在低pH和低磷酸盐浓度下与植物信号无关的virG表达不受这些突变影响。对该区域的序列分析揭示了两个不同的开放阅读框,我们将其命名为chvE和ORF1。几个转座子插入定位于chvE中;这导致毒力减弱。chvE编码一种假定的蛋白质,该蛋白质与参与趋化作用和糖摄取的两种周质受体蛋白同源。ORF1是否为毒力所必需尚不确定。一个导致无毒力的转座子插入定位于ORF1的5'端或其附近,而几个不影响毒力的转座子插入定位于其3'端。ORF1编码一种假定的蛋白质,该蛋白质与一类转录激活蛋白同源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b0/208673/886ef165f8e6/jbacter01046-0147-a.jpg

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